Tasks

- Responsible for building and developing the start-up and trial monitoring team in Germany
- Builds partnerships with FSP vendors
- Oversight of study start-up and monitoring in Germany
- Performs accompanied visits of CRAs to assess their performance
- Builds knowledge of clinical site capabilities in Germany to optimize site selection
- Establishes effective site relationships with key sites in Germany
- Collaborates with other Clinical Operations functions to support successful planning and execution of clinical trials
- Collaborates with other countries to support process improvement
- Provides ongoing mentoring and training to study start-up and trial monitoring teams
- Assists in maintaining and updating company-level investigator database
- Provides input into SOP development that impacts Monitoring Excellence
- Contributes to Clinical Operations strategy and performance against key metrics

Qualifications

- Bachelor’s degree or higher in a scientific, medical or healthcare discipline
- 12 years of experience in clinical operations
- Solid leadership and management experience, experience in therapeutic area (oncology) is highly recommended