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Jobs(38,923)/Clinical Director Role(210)/Nutrafol (13) - Sr. Clinical Research Manager
Nutrafol

Nutrafol - Sr. Clinical Research Manager

Remote - USA$150k - $150k1mo ago
RemoteSeniorNAPharmaceuticalsClinical ResearchClinical DirectorCRODocumentationProduct MarketingClinical DocumentationReportingGCP

Requirements

• 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% • Nutrafol takes into consideration a wide range of factors in final compensation decisions, including but not limited to: skill sets, experience and training, licensure and certifications, qualifications and education, and other business and organizational needs. The listed range is applicable only to the annual base salary and does not include additional perks, benefits, or applicable bonus eligibility comprising the total compensation package. • $150,000—$165,000 USD

Responsibilities

• 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

Benefits

• Fully remote work experience • Comprehensive medical, dental, and vision package, including FSA program • 401K with employer match • Quarterly Bonus Program • Two company-wide wellness breaks every day • Free lunch on us every Tuesday and Thursday via Seamless/Grubhub • Monthly wellness stipend • Monthly internet stipend • Monthly cell phone stipend • Annual learning & development stipend • Free meditation app membership (Headspace) • Free Nutrafol subscription • Pet insurance discounts and benefits • California residents may review our CCPA notice here.

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