Director Clinical Affairs
This is the employer's own posting, not a copy on a job board.
What we know
Is it still open?
Confirmed still open
Last checked 3d ago — checked against the employer's own applicant tracking system, which is the company answering directly.
We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.
How old is it?
First seen 9d ago
No source stated a posting date, so this is when the listing first reached us — which is a floor, not the real age. Last seen at its source just now.
We have tracked this listing since 23 Oct 2026 (9 days). The employer's own board has carried it every time we have read it, most recently just now.
Is it remote?
Remote
That is the location the employer filed this posting under. Quoted as written — we do not re-word the source's own location.
Who may apply?
Not stated
The description states no restriction of its own. This is the source's own tag.
Pay
$150k–170k/yr
Published by the source in its own salary field. Shown in the posting's own currency and period; we never convert.
Skills named in the ad
Recognised terms only, from a fixed vocabulary — this is what CV matching compares against.
Carried by 1 source
-
Pinpoint employer's own board first seen 9d ago · last seen just now
The listing
The Director Clinical Affairs is responsible for leading the strategic design, execution, and
oversight of clinical research and consumer study programs for Thorne’s greater Research and Development (R&D) department. The clinical and consumer study program will be designed to enable differentiated claims on Thorne’s core/existing and new products being introduced into the portfolio.
This role combines clinical trial operations management with regulatory and business alignment, ensuring that studies are executed with excellence, compliant with global standards, and generate evidence that support finished product claims for commercial products. This role will collaborate cross-functionally with Medical & Scientific Affairs, Product Development, Marketing, Legal, and Regulatory teams to ensure clinical evidence meets internal standards and external regulatory and GCP requirements.
The ideal candidate has deep expertise in operational excellence of clinical trial management, vendor/CRO management, scientific communications, evidence-based study design and execution for dietary supplement, nutritional and/or functional food products. The Director Clinical Affairs will lead the 3C Subcommittee which governs all R&D led Clinical and Consumer Perception studies end-to-end from design to completion.
RESPONSIBILITIES
- Clinical Strategy – Define and implement the clinical research roadmap aligned with product innovation and core business objectives; identify opportunities for differentiated science and evidence-based claims.
- Claims Development & Validation – Partner with Medical & Scientific Affairs, Product Development, Marketing, Legal, and Regulatory to design studies that substantiate new finished product claims and ensure claims are scientifically credible, compliant, and marketable. Translate clinical findings into product claims, business strategies, and consumer messaging.
- Clinical Operations Leadership – Oversee end-to-end planning and execution of human clinical trials, including protocol development, site and vendor selection, project timelines, budgeting, and risk management.
- Regulatory & Compliance – Ensure compliance with GCP, ICH, FDA, FTC, etc.; oversee preparation and review of study protocols, consent forms, and final reports.
- Data Integrity & Reporting – Direct data collection, analysis, and reporting processes; partner with biostatistics and medical writing teams to ensure accurate publications, regulatory submissions, and substantiated claims.
- Vendor & Stakeholder Management – Manage relationships with CROs, investigators, and academic partners to ensure high-quality performance and scientific integrity.
- Team Leadership – Build and mentor a high-performing clinical affairs and operations team; foster a culture of operational excellence, compliance, and innovation.
- Operational Excellence – Develop KPIs and performance dashboards to track study progress; continuously improve clinical workflows, efficiency, and compliance.
- Collaborate with Thorne’s R&D team on identifying and managing opportunities to publish.
- Is proficient in appropriate FTC, cGLP, cGCP, cGMP, and FDA compliance standards.
- Consistently stays current on the scientific, technical, and market trends relevant to all of Thorne’s products, initiatives, and divisions.
- Provide support for new product development, product research, and market strategy.
- Builds and leads a highly performing Clinical Affairs team, securing the best talent, developing and strengthening staff and future leaders, and providing ongoing coaching and feedback.
- Fosters a culture of continuous learning and provides growth opportunities through knowledge to teammates.
- Conducts formal and informal performance assessments of staff, including performance versus expectations and goals, behaviors and leadership potential, and seeks the same for self.
- Functions as a contributor to consumer and professional content/media as appropriate.
WHAT YOU NEED
- Bachelor’s degree in Life Sciences, Clinical Research, or related field (advanced degree preferred: MSc, PhD, MD).
- 7-10+ years of experience in clinical research and clinical operations roles in consumer-packaged goods, dietary supplements, nutritional and/or functional foods.
- Proven experience in designing and managing human clinical trials and consumer claims studies in a leadership role.
- Strong knowledge of clinical trial methodology, GCP, ICH, FDA, FTC regulations and standards.
- Expertise in project management, budgeting, vendor oversight, and risk management.
- Solid understanding of biostatistics and data integrity principles.
- Ability to communicate complex scientific data to technical, regulatory, and business stakeholders.
- Understanding of consumer-packaged goods (natural supplements and/or other) and/or pharmaceutical clinical practices.
- Experience in writing educational content for various audiences including (but not limited to), Consumers, HCP’s, etc.
WHAT WE OFFER
- Competitive compensation
- 100% company-paid medical, dental, and vision insurance coverage for employees
- Company-paid short- and long-term disability insurance
- Company- paid life insurance
- 401k plan with employer matching contributions up to 4%
- Gym membership reimbursement
- Monthly allowance of Thorne supplements
- Paid time off, volunteer time off and holiday leave
- Training, professional development, and career growth opportunities