Affiliated Board Member (Scientific)
Advarra · United States · US
Regulatory Affairs
Remote
physician
Demand62
Career growth55
Healthcare fit78
Remote potential50
Salary band
USD 58k – 97k
5-year outlook
Stable niche role with compensation likely tied to full-time IRB/regulatory responsibilities; no salary is stated, so verify range and progression. Longer-term growth depends on expanding into regulatory leadership, compliance, or research ethics oversight.
Clinical license
Not required
Applicant reach
moderate
Seniority
senior
Employment type
full-time
Date found
2026-10-29
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Eligible countries
- United States
- Profession fit
- physician
- Rate period
- Annual
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 for clinicians with IRB, research ethics, or clinical trial regulatory experience who want a non-clinical protocol-review career. Less suitable for clinicians without prior human-subjects research or regulatory exposure.
Who should apply
Physician-scientists, nurse researchers, pharmacists, dentists, and allied health professionals with clinical trial, IRB, research ethics, GCP, or regulatory review experience; IMGs with strong research/regulatory backgrounds may also fit.
CV angle
Reframe clinical and research experience around human-subjects protection, protocol review, regulatory compliance, GCP, committee service, SOP adherence, and cross-functional collaboration with sponsors, sites, and CROs. Quantify review volume or committee contributions where real; avoid claiming IRB credentials you do not have.
Skills to highlight
- IRB/human subjects research review
- Regulatory compliance
- Clinical trial protocol review
- GCP and research ethics
- SOP adherence
- Scientific/clinical expertise
- Cross-functional collaboration
- Committee presentation and documentation
Role summary
Full-time scientific board member supporting Advarra's IRB by reviewing human-subjects research protocols, ensuring regulatory compliance, attending board meetings, and advising on research ethics and clinical/regulatory issues.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.