Hartmann Young are working with a Contract Research Organisation (CRO) to identify a Medical Director – CNS.
The Medical Director (Medical Monitor) will provide medical and safety oversight of clinical trials in CNS, ensuring participant safety, regulatory compliance, and data integrity. This role requires experience in sponsor or CRO environments and the ability to support both scientific and commercial activities.
Key Duties
- Oversee trial safety; review AEs/SAEs/SUSARs, CRFs, and safety data
- Act as primary medical contact for sites, investigators, and sponsors
- Contribute to protocol design, informed consent, and risk management
- Provide input into proposals and present to clients
- Support trials across psychiatry and neurology indications (schizophrenia, depression, anxiety, Parkinson’s, Alzheimer’s, epilepsy, pain)
- Ensure compliance with FDA/ICH/GCP guidelines
Qualifications
- MD/DO/Psy.D (psychiatry/CNS focus preferred)
- 5+ years clinical research experience, including Medical Monitoring
- Strong knowledge of CNS therapeutic areas, clinical trial processes, and regulatory requirements
- Excellent communication, leadership, and client-facing presentation skills
