This is a fully remote position, open to applicants in Germany.

📋 Description

• Responsible for medical oversight at the trial level throughout the preparation, implementation, and reporting phases of clinical trials.

• Offer medical expertise and supervision from the Trial Design Outline to the Clinical Trial Report.

• Ensure the timely creation of clinical trial protocols that meet high medical quality standards.

• Contribute to risk-based quality management for trials by identifying medically relevant data and associated risks to be included in the quality and risk management plan.

• Co-author Clinical Quality Monitoring plans.

• Conduct ongoing evaluations of medical data.

⛳️ Requirements

• Medical Doctor (MD) with a preference for those with a medical thesis.

• At least 4 years of active clinical practice experience.

• Specialization in Pulmonology, Immunology, Internal Medicine, Infectious Diseases, Family Medicine, Pediatrics, Rheumatology, or Emergency Medicine.

• Experience in the pharmaceutical industry or CRO in medical or project management roles, or global pharmacovigilance functions, ideally within Clinical Development.

• Familiarity with pertinent regulations and guidelines, including ICH-GCP.

• Previous experience as a medical monitor is preferred.

• Proficiency with data visualization systems and IT platforms.

• Experience in clinical development and trials.