C

Ceribell

EEG headband device for brain monitoring

Head of Medical Affairs

Biology & BiotechPosted on Nov 11
Full-timeSunnyvale, CA, USA$310k - $395k /yr

About the Job

Requirements

  • An MD, PharmD, or PhD is required.
  • At least 10 years of progressive Medical Affairs experience in the medical device, biotechnology, or pharmaceutical industry is required.
  • At least 3–5 years of leadership experience, including a track record of designing, building, and scaling a Medical Affairs function from the ground up, is required.
  • Experience identifying, engaging, and building long-term relationships with Key Opinion Leaders and major academic societies is required.
  • Experience guiding consensus statements, clinical guidelines, and scientific publication plans is required.
  • Experience planning and moderating scientific advisory boards and clinical forums is required.
  • Ability to define strategic goals, manage departmental budgets, and recruit talent is required.
  • Understanding of FDA regulations, the AdvaMed Code of Ethics, and compliance standards for scientific exchange and non-promotional medical communications is required.
  • Ability to collaborate with Clinical Affairs, Regulatory Affairs, Legal/Compliance, and Commercial teams is required.
  • Verbal and written communication skills to translate complex clinical data into clear, scientifically accurate educational materials are required.
  • Ability and willingness to travel approximately 30–40% for national conferences, society meetings, and academic centers is required.

Responsibilities

  • Lead strategy to engage Key Opinion Leaders and societies on Medical Affairs topics that support appropriate clinical application of the product through scientific education.
  • Build relationships with leaders of relevant societies, including AES, ACNS, ACEP, SCCN, ADS, and NCS.
  • Develop a path toward guidelines and consensus statements with relevant societies.
  • Partner with Clinical to develop a scientific dissemination plan across society forums, including annual meetings, webinars, and regional meetings.
  • Define the overall medical and scientific dissemination strategy.
  • Represent Ceribell at national conferences.
  • Develop and maintain relationships with Key Opinion Leaders across relevant societies and academic centers.
  • Plan and lead advisory boards focused on Key Opinion Leader and society engagement.
  • Recruit Key Opinion Leaders and thought leaders for scientific, non-promotional speaker partnerships.
  • Lead development and medical review of scientific communications, including publications, congress materials, white papers, and clinical education content.
  • Serve as a Ceribell thought leader for scientific exchange at key forums and conferences.
  • Build the Medical Affairs organization, including recommending team structures, recruiting and mentoring future staff, and managing departmental budgets.
  • Partner with Clinical Affairs to interpret and disseminate clinical trial and real-world evidence data.
  • Collaborate with Regulatory Affairs to ensure promotional and scientific content is consistent with regulatory submissions and approved claims.
  • Work with Legal/Compliance to adhere to applicable regulations, including FDA requirements and the AdvaMed Code of Ethics, and internal compliance policies.
  • Perform other responsibilities as assigned by the Manager/Supervisor.

Desired Qualifications

  • Deep therapeutic-area expertise in neurology, neurocritical care, emergency medicine, or intensive care is highly preferred.

About the Company

Ceribell

EEG headband device for brain monitoring

Ceribell makes and sells medical devices that monitor brain activity in hospitals. Its main product is the Ceribell EEG Headband and Recorder, worn by patients and used by trained healthcare providers in clinical settings to collect EEG data. The device captures brain signals and stores them for clinicians to review; it does not diagnose conditions or send automated alerts, leaving interpretation and treatment decisions to physicians. The system is designed for time-sensitive situations, such as Nonconvulsive Status Epilepticus (NCSE), where rapid data can help guide urgent care. Revenue comes from selling the devices to healthcare facilities, with purchases made on physician orders as required by US law. Compared with competitors, Ceribell emphasizes fast, clinician-driven data collection for urgent neurological cases and does not replace clinical judgment with automated diagnoses or alerts.

Company size
201-500
Company stage
IPO
Headquarters
Mountain View, CA
Founded
2014

Recently Posted Jobs

Explore more opportunities at Ceribell

See more jobs