Clinical Research

• Responsible for the full cycle of Clinical Data Management queries
• Cooperate with Clinical Data Managers, Data Coordinators, Statistical Programmers and others
• Assist and lead operations alongside Senior CDM
• Develop project documentation, system setup, data validation processes and procedures assigned to junior staff
• Work with Senior CDM to build study milestone timelines and follow study timelines for on-time deliverables
• Assist or lead internal and external DM meetings
• Manage proactively risks and resolve or escalate issues connected to Clinical Data Management improvement or technology
• Develop understanding of CDASH and SDTM or other recognized industry standards and their impact on programming teams
• Specialize in TA-specific data capture and standards, conduct lessons learned and disseminate them across the organization
• May act as a team leader or mentor Clinical Data Management colleagues and stakeholders on operational processes
• Lead project-level activities consistent with current or previous experience in support of study delivery

Associate Clinical Data Manager – FSP

• Oversee and manage clinical trial activities according to protocol, regulatory requirements, and industry standards
• Lead clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement
• Monitor clinical trial sites for adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
• Conduct site visits to assess site performance, resolve issues, and support successful trial execution
• Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting
• Provide training and guidance to site staff and other CRAs
• Build and maintain relationships with site personnel and stakeholders to facilitate smooth trial operations

Clinical Research jobs in Greece

Associate Clinical Data Manager – FSP

Senior Clinical Research Associate