clinical study team associate (csta i) 4959797
8 Ιουλ 2026 · Pfizer Hellas
Περιγραφή Θέσης
The Clinical Study Team Associate (CSTA I) is an essential part of the Study Team and is responsible for supporting key clinical trial tasks for assigned studies to ensure compliance with timelines, Good Clinical Practice (GCP), and Pfizer SOPs. The role collaborates with global study team members and is responsible for multiple tasks that span from study start-up to study close-out which enables the efficient execution of clinical trials to high-quality standards.
The Clinical Study Team Associate (CSTA I):
Partners with the Clinical Study Team Lead (CSTL) in providing study level operational leadership and support to clinical study teams.
Partners with the Global Study Manager and the Study Manager in providing site management, monitoring and vendor operational oversight and support.
Works proactively with minimal oversight to coordinate and prioritize multiple key study tasks in support of clinical trial systems and processes.
Collaborates with global cross functional study team members of varying levels of seniority.
Uses established procedures and methodologies to ensure the completion of assigned tasks according to timelines and to required quality standards.
Requires fundamental knowledge of the principles of the role and applies these skills to achieve assigned tasks
Role Responsibilities
The Clinical Study Team Associate (CSTA I) is responsible for providing study level operational support to the Study Team from study start up to close out and submission including:
Management and oversight of Study Team shared spaces
Trial Master File (TMF) maintenance, compliance, and oversight
Management and oversight of Study Team on Demand (STOD)
Maintain Pfizer registries and systems as required to ensure compliance
Tracking and oversight of study information; follow up with functional lines as needed
Liaising with cross functional study team members to initiate and coordinate the completion of study level forms and data entry into various clinical operations applications and systems, provide study level reporting to support management of clinical trial data, clinical trial budget and timelines
Quality control of essential clinical trial documentation including components of the Clinical Study Report (CSR) and regulatory submission
Support engagement of Independent Oversight Committees
Provide support with audit and inspection readiness activities
Assist with oversight and tracking of Clinical Trial Budget spend
Provide logistical and operational support for Investigator Meetings
Coordinate the translation of documents as required
Provide status updates on key tasks and contribute to the Study Team Meetings as an active Study Team member
Provide support to study teams with system setup and maintenance
May provide support for global study team communications to sites
Here Is What You Need (Minimum Requirements):
BA/BS with any years of experience
Demonstrated ability to introduce new ideas and knowledge on all relevant Standard Operating Procedures
Ability to prioritize multiple tasks and develop strategies for the completion of all required activities
Strong organizational skills and attention to detail
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)
Excellent written and verbal communication skills
Bonus Points If You Have (Preferred Requirements):
Experience in the management of clinical trial and regulatory documents
Solid understanding of International Conference on Harmonization Good Clinical Practices and local regulations
Familiarity with applications used in clinical trials
Experience with electronic data capture systems
Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use
