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JOB SUMMARY<ul><li>This internship role is a hands-on statistical data scientist supporting study and asset teams with statistical data sciences and analytics deliverables.</li><li>Ensures excellence in the delivery of analysis ready datasets, analysis results and displays and qc work for which they are responsible.</li><li>Ensures adherence to high quality statistical data sciences principles, processes and techniques in their daily work.</li></ul>JOB RESPONSIBILITIES<ul><li>Will be learning in the space of statistical data sciences and data standards.</li><li>Accountable for their assigned work supporting the statistical data sciences leads for a particular study or asset deliverable.</li><li>Ensures appropriate documentation and QC documentation for their deliverables.</li><li>May provide supportive QC work for other statistical data scientists deliverables.</li><li>Works with statistical data sciences leads to ensure clear specifications for their deliverables are in place.</li></ul>QUALIFICATIONS / SKILLS<ul><li>Bachelor or Master (preferred) Degree in Statistics, Data Sciences, Biological Sciences, IT, or related field.</li><li>Some experience in SAS, R, or Python programming and knowledge of clinical trials would be considered as an asset.</li><li>Strong written and oral communication skills, and time management skills.</li><li>Proven ability to manage timelines.</li><li>Fluent in English.</li></ul>

Assistant, Statistical Data Scientist (Intern - 6 months fixed term)

As part of the Clinical Data &amp; Information Sciences (CDIS) group, an integral delivery unit within the Clinical Development &amp; Operations (CD&amp;O) organization, the Senior Data Manager is responsible for timely and high quality data review and query management of clinical data supporting the Pfizer portfolio.&nbsp;The SeniorData Manager develops and maintains key data management deliverables used to collect, review, monitor, and ensure the integrity of clinical data.ROLE RESPONSIBILITIES&nbsp;&nbsp;<ul><li>Serve as Lead Data Manager for one or more clinical trials assuming responsibility for CDS activities including selection and application of data acquisition standards, database design (including specification documentation and testing of clinical data collection tools, both CRF and non-CRF, using an EDC system and/or other data collection systems), development and maintenance of the Data Management Plan, data review and query management, data access and visualization, Data Management metrics reporting, database release, and submission related activities.&nbsp;</li></ul><ul><li>Independently lead the daily DM activities and allocate study DM resource in the appropriate way.&nbsp;</li></ul><ul><li>Coach junior Data Managers in the study and perform peer review of study DM's deliverables for quality control.&nbsp;&nbsp;</li></ul><ul><li>Be responsible to achieve the study DM milestone on time with good quality.&nbsp;</li></ul><ul><li>In collaboration with the Clinical Data Scientist (CDS), ensure operational excellence across all deliverables.&nbsp;</li></ul><ul><li>Ensure work carried out in accordance with applicable SOPs and working practices.&nbsp;</li></ul><ul><li>Ensure the required study-specific CDIS documents in the Trial Master File (TMF) are of high quality and are filed contemporaneously to support downstream inspection and submission readiness activities.&nbsp;&nbsp;</li></ul><ul><li>Ensure operational excellence in collaboration with CDS for application of standards, data acquisition, proactive data review and query management, data cleaning, e-data processing, data access and visualization, DM metrics reporting, database release, and submission related activities.&nbsp;</li></ul><ul><li>Ensure lessons learnt during the course of the study are documented and shared with other study teams to facilitate cross study learning.&nbsp;&nbsp;</li></ul><ul><li>Be capable to contribute on the DM related continuous improvement activities.</li></ul>QUALIFICATIONS&nbsp;&nbsp;<ul><li>Bachelor’s degree minimum requirement. &nbsp;</li><li>Minimum 3 years Data Management experience required.&nbsp;</li><li>Demonstrated knowledge of clinical development process including knowledge and understanding of the principles of GCP.&nbsp;</li><li>Demonstrated knowledge of data management processes and principles in area of responsibility.&nbsp;</li><li>Working knowledge of clinical research, FDA &amp; ICH, GCP, GCDMP, and related regulatory requirements.</li><li>Working knowledge of all phases of clinical trials and ability to assess and determine study requirement from protocol review.&nbsp;</li><li>Familiarity with MedDRA/WHO-Drug.&nbsp;&nbsp;</li><li>Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.).&nbsp;</li><li>Demonstrates strong verbal and written communication skills including ability to communicate remotely.&nbsp;&nbsp;</li><li>Proficient experience using commercial clinical data management systems and/or EDC products (e.g. Inform preferred).&nbsp;&nbsp;</li><li>Experience using data visualization tools (e.g. Spotfire,&nbsp;J-Review) preferred.&nbsp;</li><li>Experience of project management skill in terms of resource management and timeline and quality control preferred.&nbsp;</li></ul>

Senior Data Manager, Clinical Data Management Pylaia

Resource Demand Manager provides operational resource support to functional line(s) within the R&amp;D division ensuring resource requirements in support of the Research, Development and Commercial portfolios are properly planned and understood to facilitate informed decision-making and allocation of resources based on business priorities. Contributes to the achievement of business strategies and goals by partnering with applicable business SMEs across key stakeholder groups to enable and enhance operational performance through effective forecasting, planning management of organizational resources, the development of tools and processes to effectively assess resources, both internal and external through Functional Service Providers.ROLE RESPONSIBILITIES<ul><li>Supports functional lines with mix of fixed and variable headcount, 1000 resources across several resource work types and high algorithm complexity.</li><li>Ensures potential resource capacity issues (shortfalls) are surfaced and discussed in a timely fashion.</li><li>Derive demand forecasts utilizing the Planisware enterprise portfolio project management system; create variance and trend analyses.</li><li>Manages resource and cost assessments related to internal Pfizer portfolio optimization opportunities (e.g., project accelerations, PSI buy-ups, etc.) for supported Functional Lines</li><li>Partners with senior leaders and Resourcing Business Partners to ensure organizational resources are optimized and appropriately aligned to business priorities across the business functional areas.</li><li>Innovate new strategies and tools such as dashboards, metrics and KPI’s.</li><li>Utilizes business-specific portfolio and project information to facilitate portfolio and resource planning reviews and deliver the Annual Operating Plan.</li><li>Produce business performance dashboards and key metrics utilizing advanced visualizations and appropriate communications that effectively illustrate data trends</li><li>Supports multiple aspects of resource and clinical development cost management including data transformation, analysis, and reporting</li><li>Supports the development, maintenance and analysis of clinical trial cost and resource metrics to increase accuracy in assumptions in planning.</li><li>Support the delivery of holistic view of resource capacity and allocation across business functional areas.</li><li>Reinforces the value of the FTE Tracking (Activity Tracker), CRIS (Capacity Resource Information System) and Resource Planning &amp; Forecasting (RAPID) programs for the business.</li><li>Proactively surfaces potential resource and cost related issues to key stakeholders and recommends go forward actions / sourcing solutions.</li><li>Supports the partnership with Finance to coordinate the development of the annual operating budget build.</li><li>Partners with subject matter experts in business lines on the design, development, and maintenance of resource estimating assumptions (algorithms), drivers, and templates for use in generating algorithmically derived demand forecasts utilizing the PLW enterprise portfolio project management system.</li><li>Innovate new strategies and tools such as dashboards, metrics and KPI’s</li><li>Supports high-impact cross functional special projects that improve our business in the short and long term.</li><li>For certain functional areas support the assessment of quarterly Functional Service Provider (FSP) Resource Demand Plan keying on relevant business drivers to justify resource projections, summarize changes, performs and delivers analyses summarizing forecast changes and communicates to finance and budgetary stakeholders.</li></ul>QUALIFICATIONS / SKILLS<ul><li>Bachelor’s degree required, scientific or technical focus preferred, and minimum 4+ years of relevant experience (R&amp;D operational strategy and finance a plus) or Master's degree with 3+ years related experience with ability to translate complex business questions and requirements and develop effective solutions</li><li>Business experience and understanding of processes associated with operational aspects of clinical development</li><li>Expert in Excel, SQL, XML, dashboard tools (PowerBI, Spotfire, Tableau). Strong working knowledge Planisware, Business Objects and SaaS systems. Planisware certification is a plus.</li><li>Expertise in resource algorithm design and development</li><li>Ability to translate complex business questions and requirements and develop effective solutions</li><li>Ability to synthesize detailed information from multiple, disparate sources, understand the underlying data and be able to interpret and articulate key takeaways to executive leadership</li><li>Versed in data analytics, predictive modelling, AI capabilities, and able to build dashboards and reporting tools</li><li>Strong analytical skills, critical thinker, collaborator and effective communicator</li><li>Drive for results; planning; managing and measuring work</li><li>Comfortable multi-tasking; prioritizing and balancing heavy workloads</li></ul>Out of scope:<ul><li>Category management</li><li>Vendor quality and compliance</li><li>Vendor management (sourcing, RFIs/RFPs)</li></ul>

Manager, Resource Demand

The&nbsp;Director, Product Engineering&nbsp;will lead a global team of highly skilled software engineers responsible for designing, developing and sustaining enterprise-grade digital manufacturing applications and solutions. This leader will ensure engineering excellence across multiple complex and competing priorities balancing rapid delivery with stability, scalability and maintainability.&nbsp;This role requires a seasoned technical leader who can drive architectural vision, establish best practices and standards, mentor emerging engineering talent, and guide the adoption of modern technologies including AI and emerging Agentic AI paradigms. The ideal candidate combines deep software engineering expertise with strong leadership, prioritization, and a passion for enabling innovation within a complex, global organization.ROLE RESPONSIBILITIES&nbsp;The&nbsp;Director, Product Engineering&nbsp;&nbsp;colleague’s responsibilities include but are not limited to:<ul><li>Product Delivery &amp; Execution Excellence<ul><li>Oversee multiple concurrent development initatives supporting the Digital Manufacturing portfolio</li><li>Drive end-to-end solution delivery, architecture, design, development testing, deployment and sustainment</li><li>Manage competing priorities and resource allocations across projects, balancing delivery speed with quality and compliance</li><li>Partner with product managers, solution architects, and business stakeholders to align engineering coutcomes with product roadmaps</li></ul></li></ul><ul><li>Technical Architecture &amp; Best Practices<ul><li>Define and uphold modern engineering standards such as CI/CD pipelines, code reviews, automated testing, observability and secure-by-design principles</li><li>Ensure system architectures are scalable, reliable, and maintanable across global deployments</li><li>Manage technical debt and implement continuous improvement initiatives to enhance performance and efficiency</li><li>Drive alignment with enterprise architecture, data, and cybersecurity standards</li></ul></li><li>AI Enablement &amp; Technology Integration<ul><li>Partner with AI COE, Manufacturing Intelligence, Data Engineering and Platform Engineering teams to enable AI-powered features and intelligent automation</li><li>Maintain a high-level understanding of the tools, frameworks, and infrastructure supporting AI and agentic systems (e.g. LLMs, RAG pipelines, vector databases, orchestration frameworks like LangChain or Semantic Kernel)</li><li>Advocate for AI readiness within existing applications and influence the technical direction of future applications</li></ul></li><li>Engineering Leadership &amp; Team Development<ul><li>Lead and inspire a global team of software enterprise-grade digital manufacturing applications</li><li>Serve as a hands-on technical mentor guiding junior engineers, facilitating skill growth and fostering a culture of excellence</li><li>Build an inclusive, collaborative, and high-performance engineering culture centered on ownership, continuous improvement, learning and accountability</li><li>Establish clear career paths and succession planning within the team</li></ul></li><li>Governance, Compliance &amp; Performance Management<ul><li>Ensure all solutions adhere to Pfizer’s digital standards, including cybersecurity, GxP, and data integrity requirements</li><li>Establish and track engineering KPIs – delivery, velocity, system uptime, incident response times, and technical debt reduction</li><li>Drive transparency through dashboards and regular operational reviews</li></ul></li></ul>BASIC QUALIFICATIONS&nbsp;<ul><li>Bachelor’s degree in computer science, software engineering, or relevant experience</li><li>Minimum 8+ years of experience in software engineering, including full-stack or backend development in enterprise environments</li><li>Demonstrated experience leading high-performing engineering teams delivering complex, mission-critical applications</li><li>Strong technical depth in modern software architectures, APIs, microservices, and cloud-native design patterns</li><li>Proven success managing competing priorities, allocating resources effectively, and communicating tradeoffs with senior stakeholders</li><li>Experience mentoring engineers and establishing professional growth and development paths within engineering teams</li><li>Working knowledge of AI technologies and architectures including experience with LLMs, RAG vector databases, orchestration frameworks (e.g. LangChain, Semantic Kernel), or intelligent agent systems</li><li>Strong communication skills with the ability to bridge technical and business audiences</li><li>Demonstrated success operating in global, matrixed organizations</li></ul>PREFERRED QUALIFICATIONS<ul><li>Master’s degree in computer science, Engineering Management or related field</li><li>Experience with regulated or GxP environments such as pharma and medical devices</li><li>Experience in a manufacturing environment</li><li>Familiarity with MLOps and AI infrastructure (e.g. Azure AI Foundry, OpenAI API, Amazon Bedrock and Sagemaker AI, Databricks or similar ecosystems)</li><li>Strong background in agile development, preferabily SaFE, and DevOps culture</li></ul>

Director, Product Engineering

The Order to Cash Collections Analyst will form part of a virtual Global O2C Collections team reporting under the Global O2C Collections Director, Jennifer Strecker. The successful candidate will be responsible for the performance of activities such as Customer Collections and dunning, customer account management, query and dispute management. Completion of these activities will ensure that F&amp;GBS continue to support the achievement of working capital objectives and Leadership amongst other key stakeholders will have access to timely, accurate, and complete Order to Cash information. The successful candidate will receive the benefit of working for a stable and very well-established international corporation with a sonorous name and highly established organizational culture. All our colleagues become an important part of our international, friendly and dynamic team.&nbsp;ROLE RESPONSIBILITIES&nbsp;These responsibilities include but are not limited to the following:&nbsp;<ul><li>Proactively analyze AR falling due and delinquent account balances to ensure timely collection of 3rd party receivables.&nbsp;</li><li>Timely execution of customer dunning activities (e.g. outbound calls, emails, letters, etc.)&nbsp;</li><li>Coordinate customer account resolution with internal parties and execute on agreed collection strategies.&nbsp;</li><li>Timely resolution of inbound billing inquiries (calls, emails, letters, etc.,) with respective parties.&nbsp;</li><li>Maintenance of subledger. Process adjustments/write off balances (non-ADA: FX, bank charges, residuals, etc.), manage default accounts (US only) and provide guidance to Cash application on offsets and payment application where required.&nbsp;</li><li>Refund issuance (review, obtain approvals, and confirm).&nbsp;</li><li>Contribute to AR KPI reporting &amp; analysis on performance of AR ledger.&nbsp;</li><li>Research and support resolution of open disputes. Coordinate with relevant internal stakeholders and customer to support timely close-out of open disputes.&nbsp;</li><li>Effectively communicate to peers and management with regards to work tasks and deadlines.&nbsp;</li><li>Manage and resolve escalations in a timely manner ensuring appropriate management oversight where necessary.&nbsp;</li><li>Manage time effectively and communicate to peers and management with regards to work tasks, status and deadlines.&nbsp;</li><li>Proactively ensure hand-offs to supporting teams are timely and clearly communicated as part of a virtual Global Collections team i.e. Other regional hubs for Collections, Cash application, Credit Risk COE, AR Accounting &amp; Compliance, G2N etc.&nbsp;</li><li>Maintain receipt records, files and documentation in an organized manner.&nbsp;</li><li>Share audit documentation to support periodic SAP PC control performance and internal/external audit programs.&nbsp;</li><li>Participate in F&amp;GBS Order-to-Cash global initiatives including transformational projects as needed, as a subject matter expert for the area.&nbsp;</li><li>Ensure strong commitment to the control environment through training and review to meet all control and compliance requirements.&nbsp;</li></ul>QUALIFICATIONS&nbsp;Education and Experience&nbsp;<ul><li>Bachelor's Degree, Finance or Economics or Accounting strongly preferred.&nbsp;</li><li>Fluent English and Italian language requirements to support effective engagement with Customers and colleagues/business partners as needed (must have Italian language skills).&nbsp;</li><li>Up to 2 years of experience in Accounts receivable and/or broader Order to Cash function preferred.</li><li>Experience with financial shared services preferred.&nbsp;</li><li>Experience of working in cross-functional and multi-cultural team an advantage.&nbsp;</li><li>Ability to work in a high-performing team environment.&nbsp;</li><li>Strong interpersonal skills and ability to communicate with diverse groups and individuals.&nbsp;</li><li>Demonstrated ability to work on own initiative.&nbsp;</li><li>Strong verbal and written communication skills.&nbsp;</li><li>Strong business acumen and professionalism with the ability to interface effectively with all levels of management and operations colleagues in all applicable Pfizer Finance and business functional areas&nbsp;</li></ul>Technical Skills Requirements&nbsp;<ul><li>Proficiency in PC skills (MS Excel, Word, PowerPoint, Teams) required&nbsp;</li><li>SAP ERP system experience preferred including FSCM Collections, Dispute Mgt and S4 Hana.&nbsp;</li></ul>Please apply by sending your CV and a motivational letter in English

Global Ο2C Collections Analyst & Dispute Mgt - Italian (12 months fixed term)

Αναζητούμε τώρα να εντάξουμε έναν&nbsp; συνάδελφο στην ομάδα της Θεσσαλονίκης ως Junior Quality Control.&nbsp;Σκοπός ρόλουΔιασφάλιση ότι τα προϊόντα Knauf συμμορφώνονται με τα ευρωπαϊκά πρότυπα και τις εσωτερικές προδιαγραφές ποιότητας, με επίκεντρο την ασφάλεια, την αξιοπιστία και τη συνεχή βελτίωση.<ul><li></li></ul>Κύριες αρμοδιότητες<ul><li>Δειγματοληψία και έλεγχος διεργασιών (in-process) και τελικών προϊόντων βάσει Σχεδίων Ελέγχου και Οδηγιών Εργασίας.</li><li>Εκτέλεση εργαστηριακών δοκιμών και μετρήσεων.</li><li>Καταγραφή αποτελεσμάτων, στατιστική παρακολούθηση (SPC), τάσεις και αναφορές ποιότητας.</li><li>Χειρισμός μη συμμορφώσεων: άμεση απομόνωση παρτίδων, καταχώρηση NCR, διερεύνηση αιτίας (5 Why, Ishikawa) και υλοποίηση διορθωτικών/προληπτικών ενεργειών (CAPA).</li><li>Συντήρηση, βαθμονόμηση και επαλήθευση εργαστηριακού εξοπλισμού (MSA/GR&amp;R όπου απαιτείται).</li><li>Υποστήριξη και συμμόρφωση με συστήματα ISO 9001 (Ποιότητα), ISO 14001 (Περιβάλλον), ISO 45001 (Υγεία &amp; Ασφάλεια). Συμμετοχή σε εσωτερικά/εξωτερικά audits.</li><li>Ενημέρωση και τήρηση SOPs/Οδηγιών Εργασίας, Σχεδίων Ελέγχου και Φύλλων Προδιαγραφών.</li><li>Έκδοση πιστοποιητικών συμμόρφωσης/CoA και διαχείριση δειγμάτων αναφοράς (retain samples).</li><li>Συνεργασία με Παραγωγή, Συντήρηση, Εφοδιαστική Αλυσίδα και R&amp;D για βελτιώσεις διεργασιών και εγκρίσεις πρώτων υλών.</li><li>Εκπαίδευση χειριστών παραγωγής σε ελέγχους αυτοεπιθεώρησης και απαιτήσεις ποιότητας.</li><li>Τήρηση κανόνων Υγείας &amp; Ασφάλειας, 5S και καθαριότητας εργαστηρίου.</li></ul>Απαιτούμενα προσόντα<ul><li>Πτυχίο Χημείας, Χημικού Μηχανικού, Τεχνολογίας Υλικών ή συναφούς αντικειμένου. Εναλλακτικά, τεκμηριωμένη εμπειρία σε εργαστήριο QC βιομηχανίας.</li><li>2–3 χρόνια εμπειρίας σε ποιοτικό έλεγχο βιομηχανίας δομικών υλικών ή σχετικής παραγωγής.</li><li>Καλή γνώση ISO 9001 και βασικών αρχών SPC, CAPA, ιχνηλασιμότητας. Εξοικείωση με ISO 14001/45001 είναι επιθυμητή.</li><li>Γνώση σχετικών ευρωπαϊκών προτύπων (π.χ. EN 520, EN 13279, EN 998, EN 13963) και βασικών απαιτήσεων σήμανσης/συμμόρφωσης.</li><li>Εμπειρία με εργαστηριακό εξοπλισμό (ζυγοί ακριβείας, κλίβανοι ξήρανσης, ρεόμετρα/viscometers, συσκευές δοκιμών αντοχής).</li><li>Άριστη χρήση MS Excel και MS Office. Επιθυμητή εμπειρία σε SAP (ιδίως QM).</li><li>Πολύ καλή γνώση Αγγλικών (γραπτά και προφορικά).</li></ul>Ικανότητες&nbsp;<ul><li>Προσοχή στη λεπτομέρεια και τήρηση διαδικασιών.</li><li>Αναλυτική σκέψη και επίλυση προβλημάτων.</li><li>Ομαδικότητα, αποτελεσματική επικοινωνία με βάρδιες παραγωγής.</li><li>Προσανατολισμός στον πελάτη και στα αποτελέσματα.</li><li>Δέσμευση στην ασφάλεια, το περιβάλλον και τις αξίες της Knauf.</li></ul>Παροχές<ul><li>Συνεχής εκπαίδευση και ανάπτυξη.</li><li>Ιδιωτική ασφάλιση υγείας.</li><li>Ανταγωνιστικό πακέτο αποδοχών ανάλογα με προσόντα και εμπειρία.</li><li>Προοπτικές εξέλιξης εντός του Ομίλου Knauf.</li></ul>

Junior Quality Control

Αναζητούμε τώρα να εντάξουμε έναν ακόμη συνάδελφο στην ομάδα της Θεσσαλονίκης&nbsp;ως Εργάζόμενος/μενη Παραγωγής Δομικών Υλικών.Μπορείς να πεις «ναι»;...Αντιμετωπίζεις τους συναδέλφους σου με σεβασμό;Έχεις πάντα στο μυαλό σου τον πελάτη;Λειτουργείς με γνώμονα τις μελλοντικές γενιές;Σου αρέσει να αναζητάς ευκαιρίες για να αναπτυχθείς;Έχεις αποδεδειγμένο ιστορικό επίτευξης αποτελεσμάτων;Τα βασικά σου καθήκοντα περιλαμβάνουν την υποστήριξη της γραμμής παραγωγής.Με τι θα ασχολείσαι;&nbsp;<ul><li>Εργασία στις θέσεις γραμμής παραγωγή</li><li>Χειρωνακτική εργασία</li><li>Χειρισμός περονοφόρου</li><li>Πενθήμερη εργασία σε βάρδιες&nbsp;</li></ul>Τι θα θέλαμε να έχεις:Ενδιαφερόμαστε για εσένα ως άτομο, τη στάση, τις συμπεριφορές και τις αξίες σου. Εφόσον έχεις τη θέληση να μάθεις οτιδήποτε χρειάζεσαι για τον ρόλο που δεν έχεις ήδη, θέλουμε να σου μιλήσουμε:&nbsp;<ul><li>Απόφοιτος/η Λυκείου</li><li>Κάτοχος διπλώματος οδήγησης Β’ κατηγορίας</li><li>Επικοινωνία</li><li>Ευελιξία</li><li>Ομαδικότητα&nbsp;</li></ul>Παρέχουμε:<ul><li>Συνεχή εκπαίδευση</li><li>Ιδιωτική ασφάλιση</li><li>Μισθό : αναλόγως προσόντων</li></ul>Τι ακολουθεί; Εκτιμούμε ότι ο χρόνος σου είναι πολύτιμος και η υποβολή αίτησης για μια νέα θέση εργασίας μπορεί να είναι μια μακρά διαδικασία - γι' αυτό δεσμευόμαστε να απαντήσουμε στην αίτησή σου το συντομότερο δυνατόν.

Εργαζόμενος/μενη παραγωγής δομικών υλικών στο Εργοστάσιο Θεσσαλονίκης

JOB SUMMARY<ul><li>A highly productive, independent statistical data sciences lead ensuring excellence in the delivery of analysis ready datasets, analysis results, and displays such as tables, listings, and figures to advance research, development, and commercialization of the Pfizer portfolio following Pfizer SOPs and processes.</li><li>Ensures adherence to high quality statistical data sciences principles, processes and techniques in the production of clinical reports.</li><li>This role is the statistical data sciences point of contact at the study level, and will support at the asset/submission level.</li></ul>JOB RESPONSIBILITIES<ul><li>Will deliver through combination of oversight of in-house statistical data scientists / vendors / offshore support as well as through hands on application of statistical data sciences techniques (e.g., use of tools such as SAS, R, and Python to process clinical trial data and big data sources such as Real World Evidence to inform decision making).</li><li>Works with department leadership and project teams to establish strategy, timelines, and resourcing of deliverables for their study(ies).</li><li>Accountable for the quality and timely delivery of datasets, analysis results and displays required for their clinical study reports as well as other asset level deliverables they may contribute to under the leadership of the asset lead.</li><li>Ensures appropriate documentation across the lifespan of the study for deliverables and verifies proper Trial Master File filings when appropriate.</li><li>Ensures planning is in place for all deliverables including consideration of special data types and downstream uses of data.</li><li>Works with statisticians, statistical data science resources and other colleagues as appropriate to ensure clear specifications for deliverables are in place.</li><li>Will be knowledgeable in core safety standards as well as Therapeutic Area standards or Industry data standards for unique data types pertinent to their project. May aid in development of standards necessary for their study or asset.</li><li>Will contribute to department level initiatives.</li><li>Proactive at communicating potential issues to upper management.</li><li>Anticipates and solves routine problems, while developing the ability to solve complex problems using skills based on experience and extrapolation to new situations.</li><li>Supervises and supports a team, fostering collaboration and continuous improvement.</li></ul>QUALIFICATIONS / SKILLS<ul><li>Bachelor’s or Master’s (preferred) Degree in Statistics, Data Sciences, Biological Sciences, IT, or related field.</li><li>At least 5 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency.</li><li>Clinical trials expertise with a thorough understanding of data operations required for the reporting of clinical trial data.</li><li>Good understanding of ICH and Regulatory Guidelines including submission requirements and data conformance (e.g., Pinnacle21).</li><li>Statistical Programming and SAS, R, or Python hands-on experience.</li><li>Familiarity with R packages, Shiny Apps, Markdown reports and other associated data science and data analytics tools and AI/ML highly desired.</li><li>Experience with Real World Evidence and other big data sources and associated standards (e.g.OMOP, JSON, ODHSI ) in support of regulatory filings desired.</li><li>Active participation in relevant industry groups (e.g., PHUSE, CDISC, IHD).</li><li>Routine problem solving skills, developing the ability to solve complex problems using skills based on experience and extrapolation to new situations.</li><li>Thorough understanding of clinical data and relevant data standards (e.g., CDISC).</li><li>Extensive knowledge of routine statistical methodology and its application to statistical data sciences.</li><li>Knowledge of vendor processes.</li><li>Demonstrated experience in developing successful partnerships within study teams.</li><li>Strong written and oral communication skills, and project management skills.</li><li>Ability to present technical information to a non-technical audience.</li><li>Proven ability to operate independently.</li><li>Some exposure working across international boundaries and cultures.</li><li>Ability to manage customer expectations.</li><li>Ability to manage work of others in a remote and/or global setting.</li></ul>

Manager, Statistical Data Sciences Lead Thessaloniki

Η&nbsp;Creta&nbsp;Farms&nbsp;Τροφίμων, κορυφαία εταιρία στο χώρο των τροφίμων &amp; ηγέτιδα στην παραγωγή αλλαντικών, ζητά να προσλάβει:&nbsp;Οδηγό (Code:&nbsp;CF_140 )με έδρα τη Θεσσαλονίκη&nbsp;Κύριες αρμοδιότητες:<ul><li>Φορτοεκφορτώσεις οχήματος</li><li>Παραδόσεις παραγγελιών</li></ul>Απαραίτητα Προσόντα :<ul><li>Προϋπηρεσία σε αντίστοιχη θέση 2-3 έτη (θα εκτιμηθεί επιπλέον προϋπηρεσία σε τμήματα αποθηκών)</li><li>Δίπλωμα Γ’ κατηγορίας, ΠΕΙ &amp; προαιρετική η κάρτα ψηφιακού ταχογράφου</li><li>Ικανότητες οργάνωσης και τήρησης χρονοδιαγραμμάτων</li><li>Επικοινωνιακές ικανότητες και πνεύμα συνεργασίας</li></ul>Η&nbsp;Εταιρεία&nbsp;προσφέρει:<ul><li>Σύγχρονο &amp; δυναμικό εργασιακό περιβάλλον</li><li>Συνεχή υποστήριξη, ανάπτυξη και εκπαίδευση</li></ul>&nbsp;Εάν θέλετε και εσείς να γίνετε μέλος της Ομάδας μας , μπορείτε να στείλετε τα βιογραφικά σας:&nbsp;hr@cretafarm.grΓιατί η μοναδική συνταγή της Επιτυχίας μας είναι οι άνθρωποι μας !!!

CF_140 - ΟΔΗΓΟΣ ΔΙΑΝΟΜΗΣ (Θεσσαλονίκη)

Η&nbsp;KNAUF ΕΛΛΑΔΑΣ&nbsp;είναι υπερήφανη που είναι μέλος του Ομίλου Knauf. Έχουμε μια κληρονομιά 32 ετών στην παραγωγή δομικών υλικών με βάση τον γύψο και έχουμε μεγάλα σχέδια για το μέλλον. Η παγκόσμια παρουσία μας σε περισσότερες από 96 χώρες συνεχίζει να αυξάνεται και αναζητούμε παθιασμένους, φιλόδοξους ανθρώπους για να μας βοηθήσουν να επιτύχουμε τους στόχους μας.. Όλοι μας καθοδηγούμαστε από τις ίδιες βασικές αξίες και πιστεύουμε στις ισχυρές δυνατότητες των μεγάλων εταιρειών να έχουν θετικό αντίκτυπο στον κόσμο. Αναζητούμε τώρα να εντάξουμε έναν ακόμη συνάδελφο στην ομάδα της&nbsp;Θεσσαλονίκης&nbsp;ως&nbsp;Χειριστής ή Βοηθός Χειριστή ανυψωτικού μηχανήματος. Μπορείς να πεις «ναι»;...Αντιμετωπίζεις τους συναδέλφους σου με σεβασμό; Έχεις πάντα στο μυαλό σου τον πελάτη;Λειτουργείς με γνώμονα τις μελλοντικές γενιές;Σου αρέσει να αναζητάς ευκαιρίες για να αναπτυχθείς;Έχεις αποδεδειγμένο ιστορικό επίτευξης αποτελεσμάτων;&nbsp;Τα βασικά σου καθήκοντα περιλαμβάνουν την&nbsp;φορτοεκφόρτωση και την προετοιμασία των παραγγελιώνΜε τι θα ασχολείσαι;<ul><li>Εκτέλεση εργασιών φορτοεκφόρτωσης με χρήση περονοφόρων μηχανημάτων</li><li>Προετοιμασία των παραγγελιών των πελατών προς φόρτωση</li><li>Έλεγχος των αποθεμάτων και συμμετοχή στη διαδικασία απογραφής</li><li>Διασφάλιση της τήρησης των οδηγιών ασφαλούς φόρτωσης της εταιρίας και καθημερινός έλεγχος της λειτουργίας των μηχανημάτων</li><li>Τήρηση των εταιρικών κανόνων Υγείας και Ασφάλειας και συμμετοχή σε ενέργειες συνεχούς βελτίωσης</li></ul> Τι θα θέλαμε να έχεις:&nbsp;&nbsp;Ενδιαφερόμαστε για εσένα ως άτομο, τη στάση, τις συμπεριφορές και τις αξίες σου. Εφόσον έχεις τη θέληση να μάθεις οτιδήποτε χρειάζεσαι για τον ρόλο που δεν έχεις ήδη, θέλουμε να σου μιλήσουμε :&nbsp;<ul><li>Απόφοιτος Δευτεροβάθμιας Εκπαίδευσης</li><li>Κάτοχος διπλώματος οδήγησης Β’ κατηγορίας</li><li>Εμπειρία 2 ετών σε ανάλογη θέση</li><li>Δίπλωμα Χειριστή ανυψωτικού (προαιρετικό)</li><li>Επικοινωνία</li><li>Ευελιξία</li><li>Ομαδικότητα</li></ul>Παρέχουμε:&nbsp;<ul><li>Μισθό αναλόγως προσόντων</li><li>Ιδιωτική ασφάλιση υγείας</li><li>Συνεχή εκπαίδευση</li></ul>Τι ακολουθεί;Εκτιμούμε ότι ο χρόνος σου είναι πολύτιμος και η υποβολή αίτησης για μια νέα θέση εργασίας μπορεί να είναι μια μακρά διαδικασία - γι' αυτό δεσμευόμαστε να απαντήσουμε στην αίτησή σου εντός πέντε εργάσιμων ημερών.

Χειριστής/ Βοηθός Xειριστή Aνυψωτικού Mηχανήματος

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