Director Clinical Affairs
Thorne · United States · US
Clinical Research
Remote
physician
Dentist
Demand70
Career growth65
Healthcare fit62
Remote potential40
Salary band
USD 150k – 170k
5-year outlook
Senior director compensation in supplement and clinical research is likely competitive and stable, but exact pay depends on location, company size, and scope; no salary data is provided.
Clinical license
Not required
Applicant reach
narrow
Seniority
senior
Employment type
full-time
Date found
2026-10-26
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Eligible countries
- United States
- Profession fit
- physician, Dentist
- 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 only for senior clinical research or clinical affairs leaders with supplement/nutrition trial experience and CRO/vendor management backgrounds. It is not a practical entry point for clinicians without prior non-clinical clinical research leadership experience.
Who should apply
Physicians, pharmacists, nurses, or clinical research professionals with senior experience in clinical trial operations, GCP/ICH/FDA/FTC compliance, CRO management, and dietary supplement or nutrition evidence generation.
CV angle
Frame real clinical research and healthcare experience around trial leadership, protocol design, GCP/ICH/FDA/FTC compliance, CRO and vendor management, cross-functional collaboration, claims substantiation, data integrity, publications, and team leadership. Do not claim supplement-industry experience unless it is genuine.
Skills to highlight
- Clinical trial operations
- Protocol development and study design
- GCP/ICH/FDA/FTC compliance
- CRO and vendor management
- Claims substantiation
- Cross-functional leadership
- Data integrity and reporting
- Team leadership and KPIs
Role summary
Lead Thorne's clinical research and consumer study programs, including trial operations, CRO/vendor oversight, regulatory compliance, claims substantiation, data reporting, and cross-functional collaboration with R&D, medical affairs, marketing, legal, and regulatory teams.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.