Sr. Clinical Research Manager in United States at Jobgether
Explore Related Opportunities
Job Description
This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Sr. Clinical Research Manager in the United States.
This role is a high-impact clinical leadership position responsible for designing, executing, and managing end-to-end clinical research studies supporting consumer health and wellness products. You will serve as the clinical lead for in-house studies focused on substantiating product claims, safety, and efficacy within a fast-paced, innovation-driven environment. The position requires strong operational ownership across study design, regulatory submissions, data systems, and cross-functional alignment. You will collaborate closely with product, regulatory, data, and marketing teams to ensure studies are scientifically rigorous and aligned with business objectives. Operating with a high degree of autonomy, you will translate GCP principles into practical frameworks suited for real-world consumer and nutraceutical research. This is a hands-on role ideal for a seasoned clinical research professional who thrives in building and executing studies in lean, agile environments.
- Lead the full lifecycle of clinical studies from protocol development and startup through execution, analysis, and closeout.
- Design and author key clinical study documents including protocols, informed consent forms (ICFs), and case report forms (CRFs).
- Develop and manage study timelines, budgets, and operational plans while proactively identifying and mitigating risks.
- Oversee IRB submissions, amendments, and continuing reviews to ensure ethical and regulatory compliance.
- Ensure all clinical research activities adhere to GCP, ICH guidelines, and applicable human subject research regulations.
- Design and manage clinical data systems, including EDC and eTMF platforms, ensuring data integrity and accessibility.
- Collaborate cross-functionally with internal teams to align study design with product, regulatory, and business objectives.
- Provide operational oversight for study execution and ensure high-quality, compliant research delivery.
- Bachelor’s degree in a medical, life sciences, or related field.
- 10+ years of clinical research experience with full ownership of study execution.
- Proven experience in pharmaceutical, nutraceutical (VMS), or wellness industry clinical research.
- Hands-on expertise in authoring protocols, ICFs, CRFs, and managing IRB submissions independently.
- Strong knowledge of GCP, ICH guidelines, and human subject research compliance requirements.
- Experience designing and managing clinical data systems such as EDC and eTMF platforms.
- Demonstrated ability to operate in lean environments without CRO reliance and manage end-to-end studies internally.
- Strong communication, presentation, and stakeholder management skills with ability to influence cross-functional teams.
- Willingness to travel up to 20% for site visits (primarily within California).
- Competitive base salary ranging from $150,000 – $165,000 USD
- Quarterly bonus program eligibility
- Fully remote work flexibility within the United States
- Comprehensive medical, dental, and vision insurance with FSA options
- 401(k) retirement plan with employer match
- Flexible PTO and company-wide wellness breaks
- Monthly wellness, internet, and cell phone stipends
- Annual learning and development stipend
- Free access to wellness and meditation tools, plus product subscription benefits
- Pet insurance discounts and additional lifestyle perks
- Strong culture focused on innovation, autonomy, and scientific rigor.