Associate Medical Director – Study Physician, Oncology Trials
Parexel
full-time
Posted on:
Location Type: Remote
Location: Germany
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Job Level
Tech Stack
About the role
- Medically responsible at the trial level throughout the preparation, conduct and reporting phase of clinical trial
- Provide medical expertise and medical oversight from the Trial Design Outline to the Clinical Trial Report
- Ensure timely preparation of high medical quality clinical trial protocols
- Minimize 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
Requirements
- Physician (MD) (ideally with medical thesis)
- Minimum of 4 years of active clinical practice experience
- Specialization in internal medicine or general practice is 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 experienced with data visualization systems and IT systems
Benefits
- Flexible work arrangements
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical trial protocolsmedical oversightrisk managementclinical quality monitoringmedical data reviewpharmacovigilancedata visualization systemsIT systems
Soft Skills
medical expertisecommunicationcollaborationproblem-solving
Certifications
Physician (MD)