Clinical Project Manager

We are looking for a highly motivated Clinical Project Manager with a strong scientific background to lead the execution of a clinical study in a dynamic and growing environment.

Key Responsibilities

• Lead clinical study start-up and execution, including site selection and activation
• Develop clinical study protocols and contribute to authoring of statistical analysis plans and CSRs
• Manage CROs and other vendors (CRAs, labs, data management, statisticians, medical writers)
• Prepare and manage study budgets and timelines
• Plan and execute investigators’ meetings
• Support the clinical development plan and build relationships with investigators and KOLs
• Ensure accurate interpretation of clinical data and support peer-reviewed publications related to clinical studies

Requirements

• M.Sc. or Ph.D. in Life Sciences, Medicinal sciences, or related field
• Several years of experience managing clinical trials including experience in protocol development and collaboration on statistical plans
• Strong scientific orientation - thorough understanding of clinical science, statistics, and medical rationale
• Excellent English (written and verbal)