Sr. Clinical Research Manager

We’re a growing company. Everything we do, we do to help people grow into the best version of themselves. As the pioneers of hair wellness, we create clinically tested products for hair growth and provide support for people at every step of their hair journey.

Our multi-factorial approach targets key root causes of hair thinning using a patented blend of standardized vitamins, minerals and natural ingredients -- and is recommended by over 7,500 physicians and hair professionals for trusted, reliable results. We never settle, and are continuously challenging existing treatments and methodologies to advance the frontier of hair science. As we help our customers grow, we grow too -- by embracing individuality and differences, leading by example, and empowering ourselves and others with our passion for wellness and innovation.

Keep growing. It’s our mantra. Our commitment to helping anybody and everybody committed to realizing their own potential to grow.

Nutrafol is seeking a full-time Clinical Research Manager to join our team. This person will serve as the Clinical Lead for Nutrafol’s ongoing US hair nutraceutical clinical studies. The Clinical Research Manager will lead the end-to-end execution of clinical studies conducted in-house for a consumer products company. This role is hands-on and operationally embedded, with responsibility for claim substantiation support, study design, site management, data infrastructure, and execution.

This individual is expected to operate with a high degree of autonomy, building and managing clinical programs that support product claims, safety, and performance. The ideal candidate is comfortable working in a fast-moving environment and can adapt GCP principles to a range of study types, including consumer product and wellness research.

• →Develop and manage study timelines, budgets, and resource plans
• →Coordinate with internal stakeholders (e.g., product, regulatory, marketing, data) to align study objectives with business goals
• →Proactively identify risks and implement mitigation strategies
• →Author core clinical study documents, including protocols, informed consent forms (ICFs), and case report forms (CRFs)
• →Lead full study lifecycle execution from startup through closeout.
• →Prepare and manage IRB submissions, amendments, and continuing reviews
• →Ensure studies are conducted in compliance with GCP and applicable regulatory and ethical guidelines
• →Design and oversee clinical data systems, including EDC and eTMF

• Bachelor's degree in related medical field
• Minimum of 10 years' clinical research experience, with demonstrated ownership of study execution
• Experience working within a Pharmaceutical, Vitamin Mineral Supplement category or wellness brand is required
• Hands-on experience managing and executing development studies in-house; startup experience is a plus
• Direct experience authoring protocols, ICFs, and CRFs
• Proven experience managing IRB submissions and approvals independently
• Advanced presentation skills, ability to influence and articulate findings in a compelling way
• Strong working knowledge of GCP, ICH guidelines, and human subjects research requirements
• Hands-on experience designing and managing clinical data systems (EDC, eTMF)
• Experience operating without CRO support or in lean clinical environments strongly preferred
• Ability to travel for site visits within California up to 20%