Senior Clinical Research Manager

🕒 May 21

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Nutrafol

51 - 200 employees

🧘 Wellness

💄 Beauty

đŸ›ïž eCommerce

💰 $35M Series B on 2019-04

Wellness ‱ Beauty ‱ eCommerce

Nutrafol is a leading provider of hair growth supplements, known for its dermatologist-recommended, science-backed approach to whole-body wellness and hair health. Their diverse range of products is clinically tested and formulated to meet the needs of both men and women across different age groups and lifestyle choices, including options for those experiencing postpartum and menopausal changes. Nutrafol's offerings target key root causes of hair thinning, such as stress, hormones, and nutrition, with formulas that focus on comprehensive hair wellness. They emphasize the importance of understanding individual bio-specific needs and offer a personalized growth plan advisor through naturopathic doctors, ensuring visible results and overall wellness benefits.

📋 Description

‱ 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

🎯 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%

đŸ–ïž Benefits

‱ Fully remote work experience ‱ Comprehensive medical, dental, and vision package, including FSA program ‱ 401K with employer match ‱ Quarterly Bonus Program ‱ Flexible PTO ‱ 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

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