Parexel
10,000+ employees
Founded 1983
💼 Consulting
🏥 Healthcare
📦 Logistics
💰 Venture Round on 1990-01
Consulting • Healthcare • Logistics
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.
Medical Director – Study Physician
🔥 0 minutes ago
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Parexel
10,000+ employees
Founded 1983
💼 Consulting
🏥 Healthcare
📦 Logistics
💰 Venture Round on 1990-01
Consulting • Healthcare • Logistics
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
• Serve as the medical lead responsible at trial level throughout the preparation, conduct, and reporting phases of clinical trials • Provide medical expertise and oversight from the Trial Design Outline through the Clinical Trial Report • Support a single client/sponsor in the EMEA region • Ensure timely preparation of high-medical-quality clinical trial protocols while minimizing protocol amendments • Contribute to trial risk-based quality management by defining medically relevant data and related risks for quality and risk management plans • Co-author Clinical Quality Monitoring plans • Perform ongoing reviews of medical data • Act as an influential member of the wider clinical trial team
🎯 Requirements
• Physician (MD), ideally with a 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 highly desirable • Pharma industry or CRO experience in medical, project management, global pharmacovigilance, or another relevant medical function desirable • Understanding of relevant regulations and guidance, including ICH-GCP • Previous experience as a medical monitor ideally • Experience with data visualization systems and IT systems ideally • Clinical development/trials experience an additional asset
🏖️ Benefits
• Open and friendly work environment • Opportunities to develop long-term careers • Opportunity to develop within the role and take on further responsibilities • Opportunities to develop skill sets within other related departments of Parexel
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