Clinical Trial Manager
Company: SciPro Agency
- Location: Munich, Germany
- Seniority: Senior
- Employment type: Full-time
- Posted: Yesterday
- Offer language: English
Job description
We are partnering with an innovative, internationally operating biopharmaceutical company focused on the development of novel treatment solutions and advancing clinical research.
As the business continues to grow, they are looking to strengthen their clinical development team with a Clinical Safety & Medical Monitoring Specialist.
Your Responsibilities
- Ensure clinical trials comply with relevant medical safety regulations and guidelines.
- Coordinate with CROs, investigators and external partners on adverse event reporting and protocol deviations.
- Support the development of safety and medical monitoring plans.
- Review clinical trial data to identify potential safety concerns and trends.
- Contribute to the preparation and review of clinical study protocols and patient consent documentation.
- Work closely with Data Management to ensure accurate collection, analysis and reporting of safety data.
- Prepare and review study plans and periodic safety reports.
Your Profile
- Completed medical degree.
- Ideally, initial experience in clinical research or clinical trial environments.
- Familiarity with eCRFs, eDiaries and adverse event reporting is advantageous.
- Good Excel and data analysis skills.
- Experience working with CROs, investigators or external service providers is a plus.
- Strong analytical skills and excellent attention to detail.
- Structured, independent and results-oriented working style.
- Confident communication skills and ability to present findings to management.
- Fluent German and English skills (C1 or above).
