CRO-PT Contract Medical Monitor, Psychiatrist
Posted 2026-05-06
Remote, USA
Full-time
Immediate Start
- Job Description:
- Provide medical and safety oversight of clinical trials
- Monitor the safety and wellbeing of study participants
- Ensure integrity of project data according to protocols and SOPs
- Perform in-depth medical assessment through review of relevant documents
- Provide medical input for protocol design
- Participate in site initiation visits and investigator meetings
- Provide 24/7 medical consultancy support to investigators
- Prepare and review the Medical Monitoring Plan and Safety Management Plan
- Follow study status via email and participate in team meetings
- Perform review of Serious Adverse Events reported by sites
- Collaborate with site staff and finalize each event
- Review protocol deviations and support early treatment discontinuation assessments
- Requirements:
- Must have a medical degree-Psychiatrist (MD, DO or international equivalent)
- Current, active medical license is preferred but not required
- Prior clinical research experience as a medical monitor, investigator, safety physician or other applicable experience in clinical trial conduct
- A minimum of 5 years of relevant experience is required
- Clinical knowledge of the therapeutic patient populations and drug class
- Knowledge and experience working with MedDRA and WHO Drug medical dictionaries
- Broad knowledge of ICH/GCP
- Excellent verbal and written communication skills
- Ability to work in a fast-paced team environment
- Benefits:
- Remote
- Up to 20 hours per week
- Long-term project