DSMB Member (Physician)
Sitero · United States · US
Clinical Research
Remote
physician
Demand63
Career growth55
Healthcare fit74
Remote potential82
5-year outlook
Likely a senior, intermittent or committee-based consulting opportunity with variable compensation depending on trial load, sponsor, and committee commitments; exact salary is not disclosed, so clinicians should expect project- or retainer-based arrangements rather than a standard entry-level salary path.
Clinical license
Required
Applicant reach
narrow
Seniority
senior
Employment type
–
Date found
2026-11-08
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 for senior physicians with direct DSMB/DMC, Phase I, or biologic safety oversight experience. Most early- or mid-career clinicians will not meet the experience barrier, but it is a strong fit for academic or retired physician-scientists seeking remote oversight work.
Who should apply
Physician-scientists, clinical immunologists, hematologists/oncologists, infectious disease or early-phase trial specialists, and retired/academic physicians with DSMB, SRC, or first-in-human biologic safety experience.
CV angle
Frame real clinical and research experience around trial safety oversight, adverse event adjudication, risk-benefit assessment, protocol review, regulatory compliance, immunogenicity and hypersensitivity evaluation, Phase I/IND experience, and independent committee service; avoid claiming DSMB experience unless genuinely held.
Skills to highlight
- DSMB/DMC or safety review committee experience
- Phase I and first-in-human trial safety oversight
- Adverse event and immunogenicity assessment
- Advanced biologic therapy safety
- Regulatory compliance and ICH/GCP knowledge
- Risk-benefit and stopping-rule evaluation
- Protocol review and clinical research ethics
- Multidisciplinary safety discussion leadership
Role summary
A remote physician member role on Data Safety Monitoring Boards/Data Monitoring Committees, reviewing interim clinical trial data, adverse events, safety trends, and stopping rules to recommend whether studies should continue, be modified, or be terminated.
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