Medical Monitor – Study Physician – Medical Director

🔥 19 minutes ago

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Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

⚕️ Healthcare Insurance

🧬 Biotechnology

💊 Pharmaceuticals

💰 Venture Round on 1990-01

Healthcare Insurance • Biotechnology • Pharmaceuticals

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

📋 Description

• 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

• 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

• Health insurance • Competitive salary • Flexible working hours • Professional development opportunities