Medical Monitor – Study Physician – Medical Director

Parexel

Study Physician at Parexel responsible for medical oversight and expertise in clinical trials. Ensuring high quality trial protocols and contributing to risk management in a clinical development setting.

Posted 7/9/2026full-timeRemote • 🇩🇪 GermanyLeadWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

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
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

What you’ll need

Physician (MD) ideally with medical thesis
Minimum of 4 years of active clinical practice experience
Specialization in Pulmonology, Immunology, Internal Medicine, Infectious Diseases, Family Medicine, Pediatrics, Rheumatology or Emergency Medicine
Experience in pharma industry or CRO in medical or project management or global pharmacovigilance functions ideally in Clinical Development
Understanding of relevant regulations and guidance including ICH-GCP
Ideally previous experience as a medical monitor
Experience with data visualization systems and IT systems
Clinical development/trials experience

Benefits

Comp & perks

Health insurance
Competitive salary
Flexible working hours
Professional development opportunities

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

Clinical Trial Protocol DevelopmentRisk ManagementMedical Data ReviewClinical Quality MonitoringData Visualization Systems