
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.
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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.
• Provide medical monitoring and strategic medical oversight for global clinical trials • Serve as a key medical contact for sponsors, study teams, and investigator sites • Contribute to protocol development, study design, safety plans, and other clinical documents • Review clinical and safety data, including adverse events, protocol deviations, and ongoing risk assessments • Deliver medical expertise and training to project teams and support scientific integrity throughout study conduct • Collaborate with cross-functional teams to proactively identify risks and drive study success • Support regulatory safety reporting and pharmacovigilance activities • Build strong client relationships through trusted scientific and medical leadership • Contribute to business development activities, including proposals, bid defenses, and client presentations • Mentor and support colleagues while helping foster a collaborative, high-performing team culture • Travel up to 20% required
• MD or equivalent medical degree from an accredited medical school • Board-certified / Board Eligible Neurologist • Extensive adult patient care experience • Strong clinical expertise in neurodegenerative diseases • Previous experience as a pharmaceutical/biotech industry physician, Medical Monitor, or clinical trial investigator is preferred • Physicians from clinical practice or academia with a strong interest in transitioning into clinical research and drug development are encouraged to apply • Demonstrated interest in advancing innovative therapies and contributing to treatments for patients with neurological disorders • Ability to travel up to 20%
• Strong mentorship, training, and development opportunities • Continuous learning, knowledge sharing, and professional growth • Supportive environment • Collaborative, high-performing team culture
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