I am seeking a part-time, contract Medical Monitor to join a team and support the expanding portfolio of our clinical studies. This is a remote role with flexible hours. The Medical Monitor should be available for a few hours most weekdays to ensure timely review of clinical assessments and safety data.
Key Responsibilities
- Serve as the Medical Monitor for clinical psychiatry studies, primarily in mood and anxiety disorders.
- Conduct ongoing safety reviews and ensure protocol compliance, including evaluation of adverse events and patient safety data.
- Collaborate closely with internal stakeholders, including the Medical Director, Regulatory, and Operations teams.
- Partner with external collaborators such as CROs and diagnostic vendors to support study conduct and data oversight.
- Provide timely medical input and guidance to clinical and operational teams.
- Dedicate approximately up to 10 hours per week (25–40 hours per month), ideally distributed across multiple days.
- Deliver regular feedback on study progress and patient safety data.
- Start Date: ASAP, with anticipated increase hours by late March to early April as studies advance to the next phase.
Qualifications
- MD Board Certified in Psychiatry (required).
- Proven experience in clinical psychiatry trials, with a focus on mood or anxiety disorders.
- Expertise in psychiatric rating scales such as the Montgomery-Åsberg Depression Rating Scale (MADRS).
- Familiarity with psychedelic-assisted clinical trials
- Familiarity with the specific challenges and needs of clinical trials involving psychedelic treatments.
- Background in clinical development from either a sponsor or CRO perspective.
- Strong working knowledge of clinical trial operations, regulatory standards, and medical data review practices.
Role Details
- Part-time contract
- 10 per week / 25–40 per month
- Remote, flexible schedule across several weekdays
Barrington James
Website