About this role
About the Role Parexel is currently seeking an experienced Study Physician to join the UK or Germany, and be assigned to a key sponsor in the EMEA region. You will be medically responsible at the trial level throughout preparation, conduct and reporting of clinical trials, providing medical oversight from the Trial Design Outline to the Clinical Trial Report. This is a core role within the trial team dedicated to a single client. What You'll Do
- Dedicated to one client.
- Ensure timely preparation of high medical quality clinical trial protocols, minimising protocol amendments.
- Contribute to trial risk-based quality management, by defining medically relevant data and related risks integrated into the quality and risk management plan.
- Co-author Clinical Quality Monitoring plans.
- Perform ongoing reviews of medical data. What We're Looking For
- Physician (MD) ideally with medical thesis; trained in a clinical setting; minimum of 4 years of active clinical practice experience.
- Specialization in Pulmonology, Immunology, Internal Medicine, Infectious Diseases, Family Medicine, Pediatrics, Rheumatology or Emergency Medicine is highly desirable.
- Experience in pharma industry or CRO in medical or project management or global pharmacovigilance functions/ any other relevant medical function ideally in Clinical Development is desirable.
- Understanding of relevant regulations and guidance including ICH-GCP.
- Ideally previous experience as a medical monitor.
- Ideally experienced with data visualization systems and IT systems.
- Clinical development/trials experience which would be an additional asset.