Medical Director / Neurology
About The Position
Parexel is seeking an experienced Medical Director to help shape the future of clinical development within its Medical Sciences team. This role offers an opportunity to deepen understanding of complex diseases, contribute to innovative therapies, and collaborate with global experts. The position is part of a culture that values continuous learning, knowledge sharing, and professional growth, while bringing new treatments to patients. Parexel offers variety in work, partnering across therapeutic areas and with diverse sponsors. The Neurosciences team supports a broad range of studies, including Alzheimer's disease, Parkinson's disease, stroke, migraine, multiple sclerosis, rare neurologic diseases, pediatric indications, psychiatry, and gene and cell therapy programs. This is a hands-on role for a physician actively involved in all aspects of clinical development, providing medical monitoring and scientific leadership, working with sponsors, participating in study meetings, contributing to operational discussions, and driving projects forward. The company values collaborative, adaptable team members who are willing to contribute to successful clinical trials and improve patient lives. A supportive environment with strong mentorship, training, and development opportunities is provided for those transitioning from clinical practice, academia, or industry into drug development.
Requirements
- MD or equivalent medical degree from an accredited medical school.
- Board-certified / Board Eligible Neurologist with extensive adult patient care experience.
- Strong clinical expertise in neurodegenerative diseases.
- Primary focus will be on adult clinical trials, with occasional opportunities to support pediatric studies as a Medical Monitor when needed.
- Demonstrated interest in advancing innovative therapies and contributing to the development of treatments for patients with neurological disorders.
Nice To Haves
- 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.
Responsibilities
- 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.
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What This Job Offers
Job Type
Full-time
Career Level
Senior
