Sr. Clinical Research Manager

• Develop and manage study timelines, budgets, and resource plans
• Coordinate with internal stakeholders to align study objectives with business goals
• Proactively identify risks and implement mitigation strategies
• Author core clinical study documents, including protocols, ICFs, and 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 regulatory 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
• Experience in Pharmaceutical, Vitamin Mineral Supplement or wellness brand
• Hands-on experience managing and executing development studies in-house
• Direct experience authoring protocols, ICFs, and CRFs
• Proven experience managing IRB submissions and approvals independently
• Advanced presentation skills
• Strong working knowledge of GCP, ICH guidelines, and human subjects research
• Hands-on experience designing and managing clinical data systems (EDC, eTMF)
• Experience operating without CRO support or in lean clinical environments preferred
• Ability to travel for site visits within California up to 20%

Pay range: $150K - $165K

• 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 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