Nutrafol

Sr. Clinical Research Manager

Nutrafol$150K — $165K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a related medical field
  • 10+ years of clinical research experience
  • Experience in the Pharmaceutical or Vitamin Mineral Supplement category
  • Hands-on experience in executing development studies in-house
  • Proven history of authoring clinical study documents
  • Familiarity with managing IRB submissions independently
  • Strong knowledge of GCP and ICH guidelines
  • Experience in designing clinical data systems (EDC, eTMF)
  • Ability to travel for site visits within California up to 20%

Responsibilities

  • Develop and manage timelines, budgets, and resource plans for studies
  • Coordinate with internal teams to align study goals with business objectives
  • Identify risks proactively and implement effective mitigation strategies
  • Author essential clinical study documents, including protocols and ICFs
  • Lead the full lifecycle execution of clinical studies from kickoff to closeout
  • Prepare and manage IRB submissions and reviews
  • Ensure compliance with GCP and ethical guidelines for clinical research
  • Design and oversee clinical data management systems like EDC and eTMF

Benefits

  • Fully remote work experience
  • Comprehensive medical, dental, and vision package
  • 401K with employer match
  • Flexible PTO and wellness breaks
  • Monthly wellness and internet stipends
  • Free lunch on Tuesdays and Thursdays
  • Annual learning and development stipend
  • Free meditation app membership
  • Discounts on pet insurance and free Nutrafol subscription
Full Job Description
About You

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.

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


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.

Salary Range:

$150,000-$165,000 USD

Perks & 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


California residents may review our CCPA notice here.

About Nutrafol

Industry
Founded
2014

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