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As an ICF Medical Writing Project Manager, you'll lead ambitious projects that strictly adhere to timelines and quality standards. Collaborate with world-class teams to make a significant impact on patient care.

A day in the Life:
• Develops project timelines, standards, budgets, and forecasts.
• Collaborates with cross-functional teams to meet project deliverables.
• Ensures timely achievement of final deliverables.
• Advances or resolves risks to project quality, budget, or timeline.
• Ensures compliance with quality processes and requirements.

Keys to Success:
• BS/BA (preferably in a scientific field) with a minimum of 2 years of relevant experience or an advanced degree with at least 1 year of relevant experience.

Experience
• Experience managing medical writing or clinical projects.
• Experience in the pharmaceutical/CRO industry preferred.
• Proven experience in medical writing (eg, Regulatory and/or plain language).
Knowledge, Skills, Abilities
• Proficient project management skills, including budgeting and forecasting.
• Solid planning and organizational abilities.
• Excellent interpersonal and communication skills; self-motivated.
• Good knowledge of global regulatory and document development guidelines.
• Effective decision-making and problem-solving skills.
What We Offer:
As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a flexible working culture, where PPD clinical research services truly value a work-life balance. We’ve grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. We are a global organisation but with a local feel.
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

As an ICF Medical Writing Project Manager, you'll lead ambitious projects that strictly adhere to timelines and quality standards. Collaborate with world-class teams to make a significant impact on patient care. A day in the Life:• Develops project timelines, standards, budgets, and forecasts.• Collaborates with cross-functional teams to meet project deliverables.• Ensures timely achievement of final deliverables.• Advances or resolves risks to project quality, budget, or timeline.• Ensures compliance with quality processes and requirements. Keys to Success:• BS/BA (preferably in a scientific field) with a minimum of 2 years of relevant experience or an advanced degree with at least 1 year of relevant experience. Experience• Experience managing medical writing or clinical projects.• Experience in the pharmaceutical/CRO industry preferred.• Proven experience in medical writing (eg, Regulatory and/or plain language).Knowledge, Skills, Abilities• Proficient project management skills, including budgeting and forecasting.• Solid planning and organizational abilities.• Excellent interpersonal and communication skills; self-motivated.• Good knowledge of global regulatory and document development guidelines.• Effective decision-making and problem-solving skills.What We Offer:As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a&nbsp;flexible working culture, where PPD clinical research services truly value a work-life balance. We’ve grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. We are a global organisation but with a local feel.Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain&nbsp;5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

ICF Medical Writing Project Manager

Supports supply chain for global clinical trials. Ensures project/study activities are in compliance with company and client requirements.
A day in the life
Develops study specific plans for each assigned project.
Meets with internal teams to coordinate efforts, provide recommendations and risks, and update project reports/spreadsheets.
Ensures fluent communication and interaction between internal departments in order to avoid obstacles during the course of the study.
Integrates all clinical supplies activities into the supply chain to support project logistic strategy and compliance with GxP requirements.
Participates in ongoing training on new regulations
Education and Experience:
Bachelor's degree or equivalent and relevant formal academic / vocational qualification
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years).
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills and Abilities:
We require experience working in a clinical trial environment with clinical supplies.
Good English and communication skills both written and verbal
Strong interpersonal, planning, organizational, problem solving, sense of urgency and decision making skills
Demonstrated effective leadership and team building skills
Strong working knowledge of Microsoft Office suite
Strong focus on customers and attention to detail
Ability to work in team environment, as well as work independently with moderate guidance
Basic understanding of clinical supply operations
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Supports supply chain for global clinical trials. Ensures project/study activities are in compliance with company and client requirements.A day in the life<ul><li>Develops study specific plans for each assigned project.</li><li>Meets with internal teams to coordinate efforts, provide recommendations and risks, and update project&nbsp;reports/spreadsheets.</li><li>Ensures fluent communication and interaction between internal departments in order to avoid obstacles during the course of the study.</li><li>Integrates all clinical supplies activities into the supply chain to support project logistic strategy and compliance with GxP requirements.</li><li>Participates in ongoing training on new regulations</li></ul>Education and Experience:<ul><li>Bachelor's degree or equivalent and relevant formal academic / vocational qualification</li><li>Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years).</li></ul>In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.Knowledge, Skills and Abilities:<ul><li>We require experience working in a clinical trial environment with clinical supplies.</li><li>Good English and communication skills both written and verbal</li><li>Strong interpersonal, planning, organizational, problem solving, sense of urgency and decision making skills</li><li>Demonstrated effective leadership and team building skills</li><li>Strong working knowledge of Microsoft Office suite</li><li>Strong focus on customers and attention to detail</li><li>Ability to work in team environment, as well as work independently with moderate guidance</li><li>Basic understanding of clinical supply operations</li></ul>We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Associate Project Manager - Global Clinical Supplies

The Lead Statistician works with multi-disciplinary research teams to provide methodological expertise, leadership and strategic support at all stages of projects from planning to completion. This individual provides guidance to junior and middle level staff or works independently on projects requiring advanced statistical analysis, interpretation and dissemination of findings. 
This is a fully remote based role.
Essential Functions):
Statistical Analysis Plan (SAP) Development 
Drafts SAPs for projects that require use of advanced statistical methodologies
Advises junior and middle level staff on methodology and approach on projects requiring use of standard statistical methodologies
Reviews and approves SAPs projects that require use of standard statistical methodologies
Implementation & Interpretation of Analyses
Project Lead (including execution of analyses) on project requiring the use of advanced statistical methodologies
Provides guidance and advice as needed for junior and mid-level staff on projects requiring use of standard statistical methodologies
Proposal Writing and Report Preparation
Leads proposal development in familiar project-types or takes a supportive role for more complex projects
Determines technical approach, reviews proposal drafts and takes responsibility of stats components
Gets involved in client discussions
Obtains significant levels of repeat business from clients
May lead technical response to requests for proposals, generates repeat work and amendments
May identify opportunities for new work
May advise and peer-review budget
Communication with internal/external Clients
Leads meetings and discussions with clients
Acts as an escalation point for client concerns related to the project
Communicate effectively and proactively with project teams
Ability to work with and delegate to junior and mid-level staff, responsible for deliverable quality and integrity
Reviews and supports presentations by more junior staff
Consulting Expectations
Provides on-the-spot problem-solving and consulting in discussions of results
Provides methodological expertise within and outside the team
Methodological Development
Contributes to the conceptualization and development of novel/bespoke solutions to meet client project needs
Independently investigates the properties, applicability and advantages/disadvantages of both:
Methodologies developed by Evidera as bespoke solutions to client projects
Newly published methodologies, and seeks senior input when needed
May lead the development of parts of tools/macros that improve efficiency of project execution, seeking senior input when needed
Provides technical training on the developed tools within HEMA
Scientific Presence
Develops and implements scientific best practices/guidelines, product development/new methods, or deliverable standards
Supports external thought leadership through publications and workshops
Looks for opportunities to disseminate knowledge
Financial - Responsible for achieving utilization and proposal and sales target
Management - Can supervise and mentor junior and middle level staff, involvement in hiring and development of staff, conducting performance reviews. 
Education, Professional Skills & Experience
Bachelors plus 10 years hands-on experience, Masters plus 6 years hands-on experience, or Doctorate plus 3 years hands-on experience in Biostatistics, Statistics, or Related field
Strong basis in fundamental statistical concepts and methods, and expertise with techniques such as regression analysis (continuous, binary, count data), longitudinal data analysis (mixed effects linear regression), parametric and semi-parametric survival analysis, meta-analysis, indirect treatment comparisons, issues related to missing data, etc.
Practical experience in standard statistical applications in health economics such as
Standard parametric and semi-parametric survival analyses
Flexible parametric models (spline, piecewise)
ITC methods (Bucher, network meta-analyses [NMA], matching-adjusted indirect comparisons [MAICs], simulated treatment comparisons)
Country-specific utility analyses to inform CEMs
Familiarity with complex methods, including:
Projecting incomplete survival data using Bayesian parametric survival models with informative priors
Adjustment for treatment switching (rank preserving structural failure time, inverse probability of censoring weighting, two-stage estimation)
Mixture cure models
Multi-state models
Multilevel network meta-regression and fractional polynomial NMA
Surrogacy analyses
Strong statistical programming skills with standard software, including R and/or STATA/SAS
Ability to communicate analysis plans and results to clients or colleagues who may have limited background in statistics
Scientific visibility in terms of authorship of peer-reviewed publications, podium presentations and posters at conferences
Personal Skills & Competencies
Demonstrates sound professional judgment in analyzing, responding to, and resolving enquiries, issues and escalations
Work well in a team as well as independently and be able to take leadership role with regard to methodological elements in projects.
Demonstrated ability to communicate and document information effectively in written English, including the ability to produce reports, documents, emails and other written pieces which are well-organized, free from errors, and are appropriately adjusted to the characteristics and needs of the audience.
Able to create, communicate, and manage effective project plans that support the delivery of overall project objective(s); to identify, manage and guide project team members; to monitor and report on progress in an organized fashion; and to deliver the required results.
Benefits
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

The Lead Statistician works with multi-disciplinary research teams to provide methodological expertise, leadership and strategic support at all stages of projects from planning to completion. This individual provides guidance to junior and middle level staff or works independently on projects requiring advanced statistical analysis, interpretation and dissemination of findings.&nbsp;This is a fully remote based role.Essential Functions):<ul><li>Statistical Analysis Plan (SAP) Development&nbsp;</li><li>Drafts SAPs for&nbsp;projects that require use of advanced statistical methodologies</li><li>Advises junior and middle level staff on methodology and approach on projects requiring use of standard statistical methodologies</li><li>Reviews and approves SAPs projects that require use of standard statistical methodologies</li><li>Implementation &amp; Interpretation of Analyses</li><li>Project Lead (including execution of analyses) on project requiring the use of advanced statistical methodologies</li><li>Provides guidance and advice as needed for junior and mid-level staff on projects requiring use of standard statistical methodologies</li><li>Proposal Writing and Report Preparation</li><li>Leads proposal development in familiar project-types or takes a supportive role for more complex projects</li><li>Determines technical approach, reviews proposal drafts and takes responsibility of stats components</li><li>Gets involved in client discussions</li><li>Obtains significant levels of repeat business from clients</li><li>May lead technical response to requests for proposals, generates repeat work and amendments</li><li>May identify opportunities for new work</li><li>May advise and peer-review budget</li><li>Communication with internal/external Clients</li><li>Leads meetings and discussions with clients</li><li>Acts as an escalation point for client concerns related to the project</li><li>Communicate effectively and proactively with project teams</li><li>Ability to work with and delegate to junior and mid-level staff, responsible for deliverable quality and integrity</li><li>Reviews and supports presentations by more junior staff</li><li>Consulting Expectations</li><li>Provides on-the-spot problem-solving and consulting in discussions of results</li><li>Provides methodological expertise within and outside the team</li><li>Methodological Development</li><li>Contributes to the conceptualization and development of novel/bespoke solutions to meet client project needs</li><li>Independently investigates the properties, applicability and advantages/disadvantages of both:</li><li>Methodologies developed by Evidera as bespoke solutions to client projects</li><li>Newly published methodologies, and seeks senior input when needed</li><li>May lead the development of parts of tools/macros that improve efficiency of project execution, seeking senior input when needed</li><li>Provides technical training on the developed tools within HEMA</li><li>Scientific Presence</li><li>Develops and implements scientific best practices/guidelines, product development/new methods, or deliverable standards</li><li>Supports external thought leadership through publications and workshops</li><li>Looks for opportunities to disseminate knowledge</li><li>Financial - Responsible for achieving utilization and proposal and sales target</li><li>Management - Can supervise and mentor junior and middle level staff, involvement in hiring and development of staff, conducting performance reviews.&nbsp;</li></ul>Education, Professional Skills &amp; Experience<ul><li>Bachelors plus 10 years hands-on experience, Masters plus 6 years hands-on experience, or Doctorate plus 3 years hands-on experience in Biostatistics, Statistics, or Related field</li><li>Strong basis in fundamental statistical concepts and methods, and expertise with techniques such as regression analysis (continuous, binary, count data), longitudinal data analysis (mixed effects linear regression), parametric and semi-parametric survival analysis, meta-analysis, indirect treatment comparisons, issues related to missing data, etc.</li><li>Practical experience in standard statistical applications in health economics such as</li><li>Standard parametric and semi-parametric survival analyses</li><li>Flexible parametric models (spline, piecewise)</li><li>ITC methods (Bucher, network meta-analyses [NMA], matching-adjusted indirect comparisons [MAICs], simulated treatment comparisons)</li><li>Country-specific utility analyses to inform CEMs</li><li>Familiarity with complex methods, including:</li><li>Projecting incomplete survival data using Bayesian parametric survival models with informative priors</li><li>Adjustment for treatment switching (rank preserving structural failure time, inverse probability of censoring weighting, two-stage estimation)</li><li>Mixture cure models</li><li>Multi-state models</li><li>Multilevel network meta-regression and fractional polynomial NMA</li><li>Surrogacy analyses</li><li>Strong statistical programming skills with standard software, including R and/or STATA/SAS</li><li>Ability to communicate analysis plans and results to clients or colleagues who may have limited background in statistics</li><li>Scientific visibility in terms of authorship of peer-reviewed publications, podium presentations and posters at conferences</li></ul>Personal Skills &amp; Competencies<ul><li>Demonstrates sound professional judgment in analyzing, responding to, and resolving enquiries, issues and escalations</li><li>Work well in a team as well as independently and be able to take leadership role with regard to methodological elements in projects.</li><li>Demonstrated ability to communicate and document information effectively in written English, including the ability to produce reports, documents, emails and other written pieces which are well-organized, free from errors, and are appropriately adjusted to the characteristics and needs of the audience.</li><li>Able to create, communicate, and manage effective project plans that support the delivery of overall project objective(s); to identify, manage and guide project team members; to monitor and report on progress in an organized fashion; and to deliver the required results.</li></ul>BenefitsWe offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Lead Statistician, Evidera

We have a vacancy for an ICF Medical Writing Program Manager based in Bulgaria and/or Serbia.

Discover Impactful Work:
Lead patient-centric medical writing programs with a focus on Informed Consent Forms (ICFs). Manage complex projects, engage with clients, and ensure flawless delivery and quality of documents, contributing to world-class research outcomes.

A day in the Life:
• Develop and adapt project plans and timelines.
• Engage and manage client relationships.
• Collaborate with cross-functional teams.
• Monitor project progress and provide status updates.
• Mentor junior staff and ensure compliance with quality processes.

Keys to Success:
• Advanced project management skills.
• Outstanding planning and organizational abilities.
• Excellent communication, negotiation, and decision-making skills.
• In-depth knowledge of regulatory and document development guidelines.
• Proven ability to lead and mentor junior staff.

Education
• BS/BA (preferably in a scientific field) with a minimum of 8 years of relevant experience, or an advanced degree with a minimum of 6 years of relevant experience.

Experience
• Experience managing medical writing or clinical projects.
• Experience working in the pharmaceutical/CRO industry.
• Preferably, experience in medical writing (Regulatory and/or plain language).

Knowledge, Skills, Abilities
• Advanced skills in budgeting, forecasting, and resource management.
• Expert planning and organizational skills.
• Excellent interpersonal and communication skills.
What We Offer:
As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a flexible working culture, where PPD clinical research services truly value a work-life balance. We’ve grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. We are a global organisation but with a local feel.
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

We have a vacancy for an ICF Medical Writing Program Manager based in Bulgaria and/or Serbia. Discover Impactful Work:Lead patient-centric medical writing programs with a focus on Informed Consent Forms (ICFs). Manage complex projects, engage with clients, and ensure flawless delivery and quality of documents, contributing to world-class research outcomes. A day in the Life:• Develop and adapt project plans and timelines.• Engage and manage client relationships.• Collaborate with cross-functional teams.• Monitor project progress and provide status updates.• Mentor junior staff and ensure compliance with quality processes. Keys to Success:• Advanced project management skills.• Outstanding planning and organizational abilities.• Excellent communication, negotiation, and decision-making skills.• In-depth knowledge of regulatory and document development guidelines.• Proven ability to lead and mentor junior staff. Education• BS/BA (preferably in a scientific field) with a minimum of 8 years of relevant experience, or an advanced degree with a minimum of 6 years of relevant experience. Experience• Experience managing medical writing or clinical projects.• Experience working in the pharmaceutical/CRO industry.• Preferably, experience in medical writing (Regulatory and/or plain language). Knowledge, Skills, Abilities• Advanced skills in budgeting, forecasting, and resource management.• Expert planning and organizational skills.• Excellent interpersonal and communication skills.What We Offer:As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a&nbsp;flexible working culture, where PPD clinical research services truly value a work-life balance. We’ve grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. We are a global organisation but with a local feel.Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain&nbsp;5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

ICF Medical Writing Program Manager

We are looking to hire an Executive Account Director, Business Development – Biopharma.
Summarized Purpose:
Secures and retains business for PPD through professional, consultative, proactive sales activities directed at decision-makers and decision influencers at existing and new clinical sponsors. Positions PPD as a primary or preferred provider for all clinical development work to be outsourced. Qualifies deals and develops proposals including defining the solutions and recommending pricing structures to meet strategic company goals. Serves as the primary contact until work is sold, then coordinates with the relevant clinical development area(s) to ensure a successful implementation. Acts as a liaison between sponsor and company on all business development activities and requirements. Gathers data on marketing trends and competitive products/services and pricing. Mentors and trains junior level staff.
Essential Functions:
• Orchestrates RFP strategy calls, develops client proposals, prepares client presentations, and negotiates and closes contracts. Signs new business authorizations at or above assigned authorization goal.
• Makes cold calls and client visits; maintains sales database; maintains cold call and client visit activity reports.
• Ensures client satisfaction through periodic client contact; reports and develops recommendations to address client dissatisfaction; respond to all client requests.
• Mentors and trains junior level staff.
Qualifications:
Education and Experience:
Bachelor's degree or equivalent and relevant formal academic / vocational qualification
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8+ years’) or equivalent combination of education, training, & experience.
Years of experience refers to typical years of related experience needed to gain the required
knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions.
Knowledge, Skills and Abilities:
• Scientific, sales and/or marketing background with concentration in pharmaceutical/biotech area.
• Proven track record of developing mid- and high- level business contacts.
• Experience in CRO organization
• Solid sales and key accounts management experience in the area of Clinical Development Services
• Excellent interpersonal skills in order to manage and fully integrate with Operations, Finance, Bids & Contracts and Marketing, and follow-up to expand relationships and business opportunities.
• Demonstrated experience in identifying and developing sales leads, making professional presentations,
managing the sales process through close, and handling all aspects of contract negotiations.
• Understanding of sales automation systems and Microsoft Office programs.
Management Role:
No management responsibility
What we offer:
At PPD Clinical Research Services we hire the best, develop ourselves and each other, and recognise the power of being one team. We understand that you will want to grow both professionally and personally throughout your career, and therefore at PPD you will benefit from an award-winning learning and development programme, ensuring you reach your potential.  
As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a flexible working culture, where PPD Clinical Research Services truly value a work-life balance. We’ve grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. We are a global organisation but with a local feel.
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

We are looking to hire an&nbsp;Executive Account Director, Business Development – Biopharma.Summarized Purpose:Secures and retains business for PPD through professional, consultative, proactive sales activities directed at decision-makers and decision influencers at existing and new clinical sponsors. Positions PPD as a&nbsp;primary or preferred provider for all&nbsp;clinical development&nbsp;work to be outsourced. Qualifies deals and develops proposals including defining the solutions and recommending pricing structures to meet strategic company goals. Serves as the primary contact until work is sold, then coordinates with the relevant clinical development area(s) to ensure a successful implementation. Acts as a liaison between sponsor and company on all business development activities and requirements. Gathers data on marketing trends and competitive products/services and pricing. Mentors and trains junior level staff.Essential Functions:• Orchestrates RFP strategy calls, develops client proposals, prepares client presentations, and negotiates and closes contracts. Signs new business authorizations at or above assigned authorization goal.• Makes cold calls and client visits; maintains sales database; maintains cold call and client visit activity reports.• Ensures client satisfaction through periodic client contact; reports and develops recommendations to address client dissatisfaction; respond to all client requests.• Mentors and trains junior level staff.Qualifications:Education and Experience:<ul><li>Bachelor's degree or equivalent and relevant formal academic / vocational qualification</li></ul>Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8+ years’) or equivalent combination of education, training, &amp; experience.<ul><li>Years of experience refers to typical years of related experience needed to gain the required</li></ul>knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions.Knowledge, Skills and Abilities:• Scientific, sales and/or marketing background with concentration in pharmaceutical/biotech area.• Proven track record of developing mid- and high- level business contacts.• Experience in CRO organization• Solid sales and key accounts management experience in the area of Clinical Development Services• Excellent interpersonal skills in order to manage and fully integrate with Operations, Finance, Bids &amp; Contracts and Marketing, and follow-up to expand relationships and business opportunities.• Demonstrated experience in identifying and developing sales leads, making professional presentations,managing the sales process through close, and handling all aspects of contract negotiations.• Understanding of sales automation systems and Microsoft Office programs.Management Role:No management responsibilityWhat we offer:At PPD Clinical Research Services we hire the best, develop ourselves and each other, and&nbsp;recognise&nbsp;the power of being one team.&nbsp;We understand that you will want to grow both professionally and personally throughout your career, and therefore at PPD you will benefit from an award-winning learning and development&nbsp;programme, ensuring you reach your potential.&nbsp;&nbsp;As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have&nbsp;a&nbsp;flexible working culture, where PPD Clinical Research Services truly value a work-life&nbsp;balance.&nbsp;We’ve grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together.&nbsp;We are a&nbsp;global&nbsp;organisation&nbsp;but with a local feel.Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Exec Account Director, Business Development - Biopharma

We are looking for an Incident Response Leader focused on safeguarding the organization from cybersecurity threats that might or already materialized into incidents. This role ensures rapid triage, response, and mitigation of Cyber Security incidents to minimize damage and reduce recovery time. 
You will be responsible for leading an external team of SOC analysts and incident responders, forensic experts, as well as coordinating cross-functional teams to ensure the organization's resilience against emerging threats while also co-designing, maintaining and overseeing incident response strategies and processes. You will be reporting to a Cyber Incident Response Product Manager.

YOUR NEW KEY RESPONSIBILITIES:
• Oversee the entire lifecycle of cybersecurity incidents, from detection to resolution.
• Serve as the primary point of contact for managing third-party SOC and CSIRT providers to triage incidents.
• Coordinate efforts with cross-functional teams to ensure rapid containment, eradication, and recovery of compromised systems.
• Conduct post-incident analysis, documenting lessons learned and implement improvements points.
• Ensure compliance to SLAs, process adherence and process improvement to achieve operational and regulatory objectives.
• Implement industry best practices, co-develop incident playbooks with external SOC/CSIRT teams, and ensure that the organization is prepared to handle any security incidents effectively.
• Ensure incidents are prioritized and response plans are available to effectively react to relevant modern threats.
• Coordinate forensic investigations which includes acquisition and analysis of digital artifacts to determine the root cause, impact, and extent of cyber incidents to support incident response efforts.
• Lead consistent and effective advanced threat hunting based on threat intelligence feeds and against today’s threat landscape and best practices.
• Maintain clear communication channels during an incident and provide timely updates to all relevant stakeholders, including senior management.
• Support continuous training programs (e.g., tabletop exercises).
• Ensure incident response activities align with the organization’s broader business continuity and disaster recovery plans.

ARE THESE YOUR SECRET INGREDIENTS?
• 3 + years of experience in cyber security incident management.
• Strong knowledge of common attack methods, including malware, ransomware, phishing, and their mitigation strategies.
• Familiarity with Security Orchestration, Automation, and Response (SOAR) platforms to streamline incident detection and response workflows.
• Ability to lead and manage external SOC/CSIRT teams, making fast, effective decisions during crises.
• Strong documentation skills for post-incident reporting and sharing insights.
• Strong analytical thinking to continuously refine and improve incident response processes.
• Exceptional ability to communicate complex technical issues in clear, concise terms to non-technical stakeholders.
• Strong communication skills to effectively work with Vendors.

We are looking for an Incident Response Leader focused on safeguarding the organization from cybersecurity threats that might or already materialized into incidents. This role ensures rapid triage, response, and mitigation of Cyber Security incidents to minimize damage and reduce recovery time.&nbsp;You will be responsible for leading an external team of SOC analysts and incident responders, forensic experts, as well as coordinating cross-functional teams to ensure the organization's resilience against emerging threats while also co-designing, maintaining and overseeing incident response strategies and processes. You will be reporting to a Cyber Incident Response Product Manager. YOUR NEW KEY RESPONSIBILITIES:• Oversee the entire lifecycle of cybersecurity incidents, from detection to resolution.• Serve as the primary point of contact for managing third-party SOC and CSIRT providers to triage incidents.• Coordinate efforts with cross-functional teams to ensure rapid containment, eradication, and recovery of compromised systems.• Conduct post-incident analysis, documenting lessons learned and implement improvements points.• Ensure compliance to SLAs, process adherence and process improvement to achieve operational and regulatory objectives.• Implement industry best practices, co-develop incident playbooks with external SOC/CSIRT teams, and ensure that the organization is prepared to handle any security incidents effectively.• Ensure incidents are prioritized and response plans are available to effectively react to relevant modern threats.• Coordinate forensic investigations which includes acquisition and analysis of digital artifacts to determine the root cause, impact, and extent of cyber incidents to support incident response efforts.• Lead consistent and effective advanced threat hunting based on threat intelligence feeds and against today’s threat landscape and best practices.• Maintain clear communication channels during an incident and provide timely updates to all relevant stakeholders, including senior management.• Support continuous training programs (e.g., tabletop exercises).• Ensure incident response activities align with the organization’s broader business continuity and disaster recovery plans. ARE THESE YOUR SECRET INGREDIENTS?• 3 + years of experience in cyber security incident management.• Strong knowledge of common attack methods, including malware, ransomware, phishing, and their mitigation strategies.• Familiarity with Security Orchestration, Automation, and Response (SOAR) platforms to streamline incident detection and response workflows.• Ability to lead and manage external SOC/CSIRT teams, making fast, effective decisions during crises.• Strong documentation skills for post-incident reporting and sharing insights.• Strong analytical thinking to continuously refine and improve incident response processes.• Exceptional ability to communicate complex technical issues in clear, concise terms to non-technical stakeholders.• Strong communication skills to effectively work with Vendors.

Cyber Security - Incident Response Leader

YOUR NEW KEY RESPONSIBILITIES:
• Design and Implement Secure Cloud Infrastructure: Develop and enforce security architectures and practices across our cloud environments on Azure
• Identity and Access Management (IAM): Create and manage roles, permissions, and policies to ensure least privilege access.
• Data Protection: Implement encryption mechanisms for data at rest, in transit, and in use, and manage encryption keys securely.
• Threat Modeling: Analyze potential threats and vulnerabilities in cloud systems, and design countermeasures to mitigate risks.
• Security Automation: Automate security tasks using Infrastructure as Code (IaC) and other tools to improve response times and reduce human error.
• Compliance Management: Ensure cloud environments adhere to industry security best practices (e.g. CIS, CAF)
• Risk Assessment: Continuously assess risks associated with cloud services and applications, and implement risk mitigation strategies.
• Collaboration and Training: Work closely with development, operations, and business teams to foster a culture of security awareness and best practices.
• Security Documentation: Create and maintain security policies, procedures, and architecture diagrams.
• Troubleshooting and Problem Solving: Analyze, troubleshoot, and resolve complex security issues, applying effective problem-solving strategies to ensure minimal downtime and risk.
• Reporting: Prepare reports for stakeholders, highlighting security posture, and compliance status on Microsoft Defender for Cloud.

ARE THESE YOUR SECRET INGREDIENTS?
• Bachelor’s or Master’s Degree in Computer Science, Computer Engineering or Information Security.
• 3+ years of experience in cloud security, with hands-on experience in Azure.
• Strong knowledge of cloud security principles, IAM, encryption, and network security.
• Experience with security tools: Cloud-native security tools Azure Security Center/Defender for Cloud.
• Experience with automation tools for Infrastructure as Code (IaC) such as ARM templates, Terraform, or Ansible within Azure.
• Excellent problem-solving skills and the ability to work in a fast-paced environment.
• Strong communication skills to effectively convey complex security concepts to both technical and non-technical stakeholders.

HOW CAN YOU BENEFIT FROM THIS POSITION?
• Opportunity to work with the leading technologies and vendors in the area of responsibility.
•Opportunity to gain deep business understanding of FMCG industry on a group level.
•Further enhancement of your capabilities in the field of Cyber Security.
•You will be able to build international experience in a multicultural and dynamic environment.

ABOUT YOUR NEW TEAM:
We are Coca-Cola Hellenic, a growth-focused consumer goods business and strategic bottling partner of the Coca-Cola Company. We bottle, distribute and sell an unrivalled range of products in 29 markets in Europe, Africa and Eurasia. As we do, we create value for all stakeholders, support socio-economic growth and build a more positive environmental impact.
We bring together more than 30,000 people from over 70 nationalities, coming from five continents. The diversity of our markets, from mature to emerging economies, provides a wide range of attractive opportunities for growth.
We nurture our talents. We give opportunities to people across all functions and levels, as well as different geographies, backgrounds and education. We are willing to take a risk on the people we believe in, even if they don’t have the perfect experience. We have faith in what every person can be. 
And although we have so much to be proud of, we always stay humble. We believe the real magic happens – for us and for you – when we OPEN UP.


AT COCA-COLA HBC, DIVERSITY HELPS US THRIVE

Including and celebrating different people and opinions is embedded in our growth story. We are committed to fostering diverse teams that reflect the communities we serve, and to creating an inclusive environment where everyone’s unique perspectives are valued and heard. By constantly building a diverse and inclusive workplace, we enrich our decision-making and provide ever more innovative solutions and shared value.

YOUR NEW KEY RESPONSIBILITIES:• Design and Implement Secure Cloud Infrastructure: Develop and enforce security architectures and practices across our cloud environments on Azure• Identity and Access Management (IAM): Create and manage roles, permissions, and policies to ensure least privilege access.• Data Protection: Implement encryption mechanisms for data at rest, in transit, and in use, and manage encryption keys securely.• Threat Modeling: Analyze potential threats and vulnerabilities in cloud systems, and design countermeasures to mitigate risks.• Security Automation: Automate security tasks using Infrastructure as Code (IaC) and other tools to improve response times and reduce human error.• Compliance Management: Ensure cloud environments adhere to industry security best practices (e.g. CIS, CAF)• Risk Assessment: Continuously assess risks associated with cloud services and applications, and implement risk mitigation strategies.• Collaboration and Training: Work closely with development, operations, and business teams to foster a culture of security awareness and best practices.• Security Documentation: Create and maintain security policies, procedures, and architecture diagrams.• Troubleshooting and Problem Solving: Analyze, troubleshoot, and resolve complex security issues, applying effective problem-solving strategies to ensure minimal downtime and risk.• Reporting: Prepare reports for stakeholders, highlighting security posture, and compliance status on Microsoft Defender for Cloud. ARE THESE YOUR SECRET INGREDIENTS?• Bachelor’s or Master’s Degree in Computer Science, Computer Engineering or Information Security.• 3+ years of experience in cloud security, with hands-on experience in Azure.• Strong knowledge of cloud security principles, IAM, encryption, and network security.• Experience with security tools: Cloud-native security tools Azure Security Center/Defender for Cloud.• Experience with automation tools for Infrastructure as Code (IaC) such as ARM templates, Terraform, or Ansible within Azure.• Excellent problem-solving skills and the ability to work in a fast-paced environment.• Strong communication skills to effectively convey complex security concepts to both technical and non-technical stakeholders. HOW CAN YOU BENEFIT FROM THIS POSITION?• Opportunity to work with the leading technologies and vendors in the area of responsibility.•Opportunity to gain deep business understanding of FMCG industry on a group level.•Further enhancement of your capabilities in the field of Cyber Security.•You will be able to build international experience in a multicultural and dynamic environment. ABOUT YOUR NEW TEAM:We are Coca-Cola Hellenic, a growth-focused consumer goods business and strategic bottling partner of the Coca-Cola Company. We bottle, distribute and sell an unrivalled range of products in 29 markets in Europe, Africa and Eurasia. As we do, we create value for all stakeholders, support socio-economic growth and build a more positive environmental impact.We bring together more than 30,000 people from over 70 nationalities, coming from five continents. The diversity of our markets, from mature to emerging economies, provides a wide range of attractive opportunities for growth.We nurture our talents. We give opportunities to people across all functions and levels, as well as different geographies, backgrounds and education. We are willing to take a risk on the people we believe in, even if they don’t have the perfect experience. We have faith in what every person can be.&nbsp;And although we have so much to be proud of, we always stay humble. We believe the real magic happens – for us and for you – when we OPEN UP. AT COCA-COLA HBC, DIVERSITY HELPS US THRIVE Including and celebrating different people and opinions is embedded in our growth story. We are committed to fostering diverse teams that reflect the communities we serve, and to creating an inclusive environment where everyone’s unique perspectives are valued and heard. By constantly building a diverse and inclusive workplace, we enrich our decision-making and provide ever more innovative solutions and shared value.

Security Engineer – Cloud

We are offering a great work experience in amazing Athens, Greece for a role as a Danish Customer Advisor.
 
Why a Customer Advisor role is great for your professional and personal development:
Live in Greece and embrace multicultural experiences
Represent a global brand
Fast-track career development opportunity
 
How your day-to-day in this role will look like: 
 
Specialist training for the product/service
You will:
Assist customer’s inquiries
Guide customers on their questions for the best use of the product/service
Maintain a high level of quality in each case you review
 
Requirements
What do you need to be successful at this job?
Language Maestro: Fluent in Danish, good English
Tech Savvy: Curious about the latest tech
Customer Charmer: Experience is a bonus
Communication Virtuoso
Empathy Expert
Benefits
Joyful Greece
Skyrock Growth starting with a permanent contract
Greek Extra Delights: Meal Card Voucher + 2 extra salaries (14 salaries annually)
Guardians of Wellness: Private health insurance from day 1
Language bonus + Performance bonus
 
Relocation Package is included:
Flight to the Future: Paid flight expenses
First-Class Arrival: Airport pick-up and settling assistance
Nest in Comfort: Accommodation is provided in hotel or apartment for the first 2 weeks
Finding your place: Real Estate agency support to find accommodation + agency covered by the company
 
Make it your Next Job Without Boundaries!

We are offering a great work experience in amazing Athens, Greece for a role as a Danish Customer Advisor.&nbsp;Why a Customer Advisor role is great for your professional and personal development:<ul><li>Live in Greece and embrace multicultural experiences</li><li>Represent a global brand</li><li>Fast-track career development opportunity</li></ul>&nbsp;How your day-to-day in this role will look like:&nbsp;&nbsp;<ul><li>Specialist training for the product/service</li><li>You will:</li><li>Assist customer’s inquiries</li><li>Guide customers on their questions for the best use of the product/service</li><li>Maintain a high level of quality in each case you review</li></ul>&nbsp;RequirementsWhat do you need to be successful at this job?<ul><li>Language Maestro: Fluent in Danish, good English</li><li>Tech Savvy: Curious about the latest tech</li><li>Customer Charmer: Experience is a bonus</li><li>Communication Virtuoso</li><li>Empathy Expert</li></ul>Benefits<ul><li>Joyful Greece</li><li>Skyrock Growth starting with a permanent contract</li><li>Greek Extra Delights: Meal Card Voucher + 2 extra salaries (14 salaries annually)</li><li>Guardians of Wellness: Private health insurance from day 1</li><li>Language bonus + Performance bonus</li></ul>&nbsp;Relocation Package is included:<ul><li>Flight to the Future: Paid flight expenses</li><li>First-Class Arrival: Airport pick-up and settling assistance</li><li>Nest in Comfort: Accommodation is provided in hotel or apartment for the first 2 weeks</li><li>Finding your place: Real Estate agency support to find accommodation + agency covered by the company</li></ul>&nbsp;Make it your Next Job Without Boundaries!

Finnish Customer Advisor – Remote

We are seeking a candidate for the position of Technical Writer for the preparation of the technical portion of Scientific Research and Experimental Development (SR&ED) tax credit claims for the Canada Revenue Agency (CRA). These claims are prepared for the benefit of Canadian companies who undertake research and development projects and are coordinated by a team from the Montreal, Canada office of Grant Thornton (RCGT). 
The successful candidate will be responsible for analyzing technical documentation provided by the client, including internal records and recorded interviews with specialists involved in the project. Based on this information and following drafting strategies outlined by the RCGT manager, the candidate will prepare technical reports that address key elements such as the technological limitations faced by the project, the work undertaken to address these challenges, and the technological advancements achieved as a result.
The position is for full-time employment through Grant Thornton Greece and will be working exclusively with the RCGT team in Montreal, remotely.
The candidate will be mentored and trained by engineers and scientists at the forefront of the field of tax incentives for technological development. The position involves drafting a technical report which relates the key elements of the client’s project.
Who You Are: Skills & Experience

A relevant academic background in Computer Science or Information Technology;
Fluency in English (CEFR C1-C2, proficient user spoken and written), as the deliverable will be a technical report;
Mastery of Informatics / Computer Science technologies and associated scientific language;
The candidate must be able to quickly understand projects involving, but not limited to, research in the following fields:
Programming and algorithms (artificial intelligence);
Platforms (SaaS, e-commerce, deployment, scaling);
Infrastructures (distributed architectures, cloud computing);
Multimedia (game engines, rendering technologies, real-time);
Telecoms (electronics, signal processing, embedded code).
This role requires a solid understanding of many different technological verticals and a capacity to synthesize information into a concise report which reflects the key elements of a project.
What’s in it for You?
At Grant Thornton Greece, we believe that great work deserves great rewards! Here’s what you can look forward to:
🌈 Diverse and inclusive workplace
🏋️‍♂️ Friendly, Dynamic Working environment
💰 Competitive Salary & Bonus
🩺 Insurance Program for all GT members
👩‍🏫 Fully funded Training & Professional Qualifications
🏖 Extra Days-off: August Freedays, Volunteering Days, Early leave days
🏃🏽‍♂️ Corporate Sports Teams (e.g., Running, Basketball, Volleyball)
🎁 Exclusive Discounts: Special offers and discounts for employees
🚗 Company Car (depending on job level)
Ready to Go Beyond?
If you're imagining a career that’s anything but ordinary, then Grant Thornton Greece is the place for you! We don’t just do business as usual—we go beyond. Ready to take that leap?
Simply upload your up-to-date CV, hit "apply", and we’ll handle the rest! ✨
We are Grant Thornton. We go beyond business as usual, so you can too.
#WelcomeToMore #GoBeyondWithUs

We are seeking a candidate for the position of&nbsp;Technical Writer&nbsp;for the preparation of the technical portion of Scientific Research and Experimental Development (SR&amp;ED) tax credit claims for the Canada Revenue Agency (CRA). These claims are prepared for the benefit of Canadian companies who undertake research and development projects and are coordinated by a team from the Montreal, Canada office of Grant Thornton (RCGT).&nbsp;The successful candidate will be responsible for&nbsp;analyzing technical documentation&nbsp;provided by the client, including internal records and recorded interviews with specialists involved in the project. Based on this information and following drafting strategies outlined by the RCGT manager, the candidate will&nbsp;prepare technical reports&nbsp;that address key elements such as the technological limitations faced by the project, the work undertaken to address these challenges, and the technological advancements achieved as a result.The position is for full-time employment through Grant Thornton Greece&nbsp;and will be working exclusively with the RCGT team in Montreal, remotely.The candidate will be mentored and trained by engineers and scientists at the forefront of the field of tax incentives for technological development. The position involves drafting a technical report which relates the key elements of the client’s project.Who You Are: Skills &amp; Experience<ul><li> </li><li>A relevant academic background in Computer Science or Information Technology;</li><li>Fluency in English (CEFR C1-C2, proficient user spoken and written), as the deliverable will be a technical report;</li><li>Mastery of Informatics / Computer Science technologies and associated scientific language;</li><li>The candidate must be able to quickly understand projects involving, but not limited to, research in the following fields:</li></ul><ol><li>Programming and algorithms (artificial intelligence);</li><li>Platforms (SaaS, e-commerce, deployment, scaling);</li><li>Infrastructures (distributed architectures, cloud computing);</li><li>Multimedia (game engines, rendering technologies, real-time);</li><li>Telecoms (electronics, signal processing, embedded code).</li></ol><ul><li>This role requires a solid understanding of many different technological verticals and a capacity to synthesize information into a concise report which reflects the key elements of a project.</li></ul>What’s in it for You?At Grant Thornton Greece, we believe that great work deserves great rewards! Here’s what you can look forward to:<ul><li>🌈&nbsp;Diverse and inclusive workplace</li><li>🏋️‍♂️ Friendly, Dynamic Working environment</li><li>💰&nbsp;Competitive Salary &amp; Bonus</li><li>🩺&nbsp;Insurance Program for all GT members</li><li>👩‍🏫&nbsp;Fully funded Training &amp; Professional Qualifications</li><li>🏖&nbsp;Extra Days-off: August Freedays, Volunteering Days, Early leave days</li><li>🏃🏽‍♂️ Corporate Sports Teams&nbsp;(e.g., Running, Basketball, Volleyball)</li><li>🎁&nbsp;Exclusive Discounts:&nbsp;Special offers and discounts for employees</li><li>🚗&nbsp;Company Car&nbsp;(depending on job level)</li></ul>Ready to Go Beyond?If you're imagining a career that’s anything but ordinary, then&nbsp;Grant Thornton Greece&nbsp;is the place for you! We don’t just do business as usual—we go beyond. Ready to take that leap?Simply upload your&nbsp;up-to-date CV, hit "apply", and we’ll handle the rest! ✨We are Grant Thornton. We go beyond business as usual, so you can too.#WelcomeToMore #GoBeyondWithUs

Technical Writer – Scientific Research & Experimental Development (SR&ED) Tax Incentive Program

According to our flexibility policy "Wherever Works", we are looking for people based anywhere in Greece who can work 100% remotely and report to our headquarters in Athens.
The opportunity
Assist in the creation of the system design and functional specifications
Drafting technical specifications for the several stages of the implementation project;
Design, implementation, testing and documentation of enterprise level tailor made multi-tier applications
Implement integration with third party applications / data sources
Utilise various workflow, document management, content management, portal systems / frameworks
Active contribution in business development activities, participating in meetings/presentations with clients, participating in the RFP process, preparing the necessary documentation
What we are looking for:
At least four (4) years of relevant professional experience in Software Development using .NET technologies
Bachelor or Master degree in IT Engineering, Computer Science, Applied Sciences or related discipline
Excellent programming skills in Object-oriented development and experience in .NET an/or .NET Core and related frameworks
Sound knowledge of Asp.Net, Asp.Net Core and Core WebAPI
In-depth knowledge of Databases and SQL (mainly MS SQL Server and/or Oracle DB, MySQL)
Sound knowledge of client-server architecture and web services (SOAP/REST)
The ability to use Design patterns and produce clean, maintainable and self-documented code is a must
Be familiar with Azure DevOps or similar platform (i.e. Atlassian JIRA, GitHub, GitLab)
Proven experience in Scrum Methodology
Ability to use modeling languages (e.g. UML) for data modeling, design of business workflows and other types of diagrams
Strong understanding of Multithreaded applications and High Performance web applications
Sound knowledge of automated unit/integration testing processes and related frameworks (e.g. nUnit, xUnit, Specflow, Selenium or other)
Any technical knowledge of Cloud environments and architecture (Azure or AWS) is considered a plus.
Any experience with React, Angular 2+, JavaScript, TypeScript, jQuery, CSS is considered a plus.
 
What’s in it for you 
At PwC is all about people, encouraging high performance and quality work.
Being part of our team includes:
🕑 Hybrid working model
💸 Competitive total compensation package
🏥 Health and life insurance 
🤵 Dress for the day - wear what makes you feel comfortable and dress for your day
💻 Company mobile phone and laptop 
🌴 Extra days of annual leave
🧘🏼 Wellness Initiatives like gym sessions & nutritionist
🏃🏽‍♂️ Actions Teams eligible to participate (e.g. Running, Trekking) 
📚 Career development opportunities & continuous training whilst learning from a wide range of top professionals and through tailor made training programmes
🌎 Global mobility opportunities
If you're looking for a team that values your work and solves meaningful problems, apply now!
We believe the best work is human-led and tech-powered. If you’re keen to apply and need reasonable adjustments or would like to note which pronouns you use at any point in the application or interview process, please let us know.

According to our flexibility policy "Wherever Works", we are looking for people based anywhere in Greece who can work&nbsp;100% remotely&nbsp;and report to our headquarters in Athens.The opportunity<ul><li>Assist in the creation of the system design and functional specifications</li><li>Drafting technical specifications for the several stages of the implementation project;</li><li>Design, implementation, testing and documentation of enterprise level tailor made multi-tier applications</li><li>Implement integration with third party applications / data sources</li><li>Utilise various workflow, document management, content management, portal systems / frameworks</li><li>Active contribution in business development activities, participating in meetings/presentations with clients, participating in the RFP process, preparing the necessary documentation</li></ul>What we are looking for:<ul><li>At least four (4) years of relevant professional experience in Software Development using .NET technologies</li><li>Bachelor or Master degree in IT Engineering, Computer Science, Applied Sciences or related discipline</li><li>Excellent programming skills in Object-oriented development and experience in .NET an/or .NET Core and related frameworks</li><li>Sound knowledge of Asp.Net, Asp.Net Core and Core WebAPI</li><li>In-depth knowledge of Databases and SQL (mainly MS SQL Server and/or Oracle DB, MySQL)</li><li>Sound knowledge of client-server architecture and web services (SOAP/REST)</li><li>The ability to use Design patterns and produce clean, maintainable and self-documented code is a must</li><li>Be familiar with Azure DevOps or similar platform (i.e. Atlassian JIRA, GitHub, GitLab)</li><li>Proven experience in Scrum Methodology</li><li>Ability to use modeling languages (e.g. UML) for data modeling, design of business workflows and other types of diagrams</li><li>Strong understanding of Multithreaded applications and High Performance web applications</li><li>Sound knowledge of automated unit/integration testing processes and related frameworks (e.g. nUnit, xUnit, Specflow, Selenium or other)</li><li>Any technical knowledge of Cloud environments and architecture (Azure or AWS) is considered a plus.</li><li>Any experience with React, Angular 2+, JavaScript, TypeScript, jQuery, CSS is considered a plus.</li></ul>&nbsp;What’s in it for you&nbsp;At PwC is all about people, encouraging high performance and quality work.Being part of our team includes:<ul><li>🕑 Hybrid working model</li><li>💸 Competitive total compensation package</li><li>🏥 Health and life insurance&nbsp;</li><li>🤵&nbsp;Dress for the day - wear what makes you feel comfortable and dress for your day</li><li>💻 Company mobile phone and laptop&nbsp;</li><li>🌴 Extra days of annual leave</li><li>🧘🏼 Wellness Initiatives like gym sessions &amp; nutritionist</li><li>🏃🏽‍♂️ Actions Teams eligible to participate (e.g. Running, Trekking)&nbsp;</li><li>📚 Career development opportunities &amp; continuous training whilst learning from a wide range of top professionals and through tailor made training programmes</li><li>🌎 Global mobility opportunities</li></ul>If you're looking for a team that values your work and solves meaningful problems, apply now!We believe the best work is human-led and tech-powered. If you’re keen to apply and need reasonable adjustments or would like to note which pronouns you use at any point in the application or interview process, please let us know.

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Θέσεις Εργασίας - Ελλάδα

(177 Αποτελέσματα)

Εξ αποστάσεως

Thermo Fisher Scientific

icf medical writing project manager

Ελλάδα

Thermo Fisher Scientific

associate project manager - global clinical supplies

Ελλάδα

Thermo Fisher Scientific

lead statistician, evidera

Ελλάδα

Thermo Fisher Scientific

icf medical writing program manager

Ελλάδα

Thermo Fisher Scientific

exec account director, business development - biopharma

Ελλάδα

Coca-Cola HBC

cyber security - incident response leader

Ελλάδα

Coca-Cola HBC

security engineer – cloud

Ελλάδα

Atlean World

finnish customer advisor – remote

Αττική

Grant Thornton Greece

technical writer – scientific research & experimental development (sr&ed) tax incentive program

Αττική

PwC Greece

senior .net developer - θεσσαλονίκη

Θεσσαλονίκη

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