Senior CRA
You will be responsible for:
- Overseeing and managing clinical site monitoring activities
- Participate in the planning and execution of clinical studies
- Reviewing and managing teams
- Ensuring compliance with plans (clinical monitoring)
- Supporting the project manager with site data, recruitment strategy, data trends, etc.
- Proactively identifying risky issues and providing actionable plans for mitigation
- Attending meetings as required: study-related, company, external, departmental meetings, etc.
- Reviewing trip reports from CRO monitors
- Performing ongoing reconciliation of the Trial Master File (TMF) with content from site files
You will have:
- Bachelor's degree in the life sciences
- Strong background and knowledge of clinical research process
- Ability to handle multiple responsibilities and prioritise effectively
- Ability to work closely with monitors and CRAs and be supportive
- Knowledge of current regulations
- Experience as a CRA
- Experience in a CRO
- German-language skills
Benefits:
- Being part of a dedicated, enthusiastic team committed to bettering the lives of patients
- Free fruit and breakfast
- Bonus package and other benefits