Medical Monitor (US Board-Certified Psychiatrist)
PSI CRO · United States · US
Clinical Research
Remote
physician
Demand72
Career growth65
Healthcare fit58
Remote potential60
5-year outlook
Senior CRO medical monitor roles typically offer competitive, stable compensation tied to MD/board-certified expertise, but exact pay varies by location, sponsor, and experience; the posting provides no salary data.
Clinical license
Required
Applicant reach
narrow
Seniority
senior
Employment type
–
Date found
2026-10-29
Intelligence details
Flexible work details
- Side income
- Classified as side-income friendly
- Engagement type
- Contract
- Hours
- Variable hours
- Eligible countries
- United States
- Profession fit
- physician
- Rate period
- Annual
Why this was classified this way
- Contractor
Listing via Himalayas.
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth considering only if you are a US board-certified psychiatrist with 10+ years of practice and want a CRO-based medical monitoring career; most early-career clinicians will not meet the bar.
Who should apply
US board-certified psychiatrists with at least 10 years of practicing experience, especially those with clinical research, safety, pharmaceutical, or CRO exposure and interest in trial medical oversight.
CV angle
Emphasize board-certified psychiatric practice, patient safety and risk assessment, quality/protocol compliance, teaching and training, and any real exposure to clinical trials, safety reporting, IRB/regulatory processes, or data review; do not claim monitoring experience you do not have.
Skills to highlight
- Medical monitoring
- Pharmacovigilance and safety reporting
- Clinical trial protocol review
- Regulatory and IRB/IEC communication
- Psychiatric therapeutic expertise
- Risk management
- Cross-functional team training
- Clinical study report review
Role summary
A senior CRO medical monitor role providing psychiatric and medical safety oversight across clinical trials, including safety narrative review, protocol deviation review, regulatory/IRB responses, committee participation, and sponsor/client interactions.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.