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← Ceribell, Inc

Director, Clinical Affairs (Hybrid - Sunnyvale)

Ceribell, Inc
Location
Sunnyvale, CA
Posted
19 days ago
Department
Clinical
What they actually want (must-haves)
  • Bachelor’s degree in a life science, engineering, or related discipline
  • Minimum of 8+ years of progressive experience in Clinical Research/Affairs within the medical device industry
  • Proven track record in designing, executing, and reporting pivotal, randomized clinical trials for medical devices
  • Deep, working knowledge of FDA regulations (CFR Title 21), ICH-GCP, and ISO 14155
Nice to have
  • An advanced degree (Ph.D., M.D., Pharm.D., or Master’s) is highly preferred
What the job really is

The Director of Clinical Affairs at Ceribell will lead the clinical evidence strategy for new products, focusing on the planning and execution of clinical trials. This role involves collaborating with various teams to ensure alignment with regulatory requirements and business goals, managing relationships with key opinion leaders, and overseeing the design and reporting of clinical protocols and data submissions.

Benefits
  • Performance-based incentive compensation (varies by role)
  • Equity opportunities
  • 100% Employer paid Health Benefits for Employees
  • 50% - 70% Employer paid Health, Dental & Vision for dependents (depending on plan selection)
  • 100% paid Life and Long-Term Disability Insurance
  • 401(k) with a generous company match
Things to weigh
  • No specific details on the company's current projects or technologies beyond the Ceribell System
  • The role requires managing multiple projects in a fast-paced environment, which may involve shifting priorities
  • The compensation range is broad and dependent on various factors, which may lead to variability in offers
Job score3.6/5
Benefits5/5
Freshness4/5
Career value4/5
Role clarity5/5
Pay transparency0/5

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