Knownwell delivers the best AI-powered client retention platform for businesses, empowering companies with intelligent insights and data-driven decision-making for growth. Backed by a16z.
About the role
👋 Meet knownwell , weight-inclusive healthcare for all . Join a dynamic company that is changing the way obesity care is delivered. We offer weight management, primary care, nutrition counseling, and health coaching. Our care model combines in-clinic and virtual care to bring support to patients where and when they need it. Found on 1752vc Careers, the job board for startup and VC roles.
What they're looking for
- 3+ years of experience in clinical research and industry environments. 2+ years of experience with independent trial management preferred
- Solid understanding of drug development processes, FDA, and ICH GCP guidelines
- Proficiency in using multiple software systems and computer technology
- Strong preference for candidates with expert phlebotomy skills
- Strong organizational, leadership, and time-management skills
- Excellent written and verbal communication skills
More about this role
👋 Meet knownwell , weight-inclusive healthcare for all . Join a dynamic company that is changing the way obesity care is delivered. We offer weight management, primary care, nutrition counseling, and health coaching. Our care model combines in-clinic and virtual care to bring support to patients where and when they need it.
Backed by $50M in funding—including a $25M round led by CVS Health Ventures with support from a16z Bio + Health, Flare Capital, MassMutual, and Intermountain Ventures—we’re scaling fast and expanding access to evidence-based obesity care nationwide.
🔍 The Clinical Research Coordinator (CRC) is responsible for overseeing and coordinating all aspects of clinical trials, ensuring that studies are conducted in compliance with regulatory requirements, sponsor expectations, and Good Clinical Practice (GCP) guidelines. The CRC will act as the primary liaison between the clinical research team, patients, and external stakeholders, ensuring the efficient and timely execution of clinical research projects.
On-site Requirements : Primarily on-site (4-5 days/wk)
*knownwell does not offer relocation assistance*
Coordinate and manage all aspects of clinical trials, including...
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