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Gilead Sciences

Makes medicines for HIV, liver disease and cancer

Director Patient Safety

Physicians & SurgeonsConfirmed live in the last 24 hours
Full-timeFoster City, CA, USAIn-person

About the Job

Requirements

  • An MD/DO degree or equivalent is required.
  • Completion of an accredited medical or surgical residency program is preferred.
  • A minimum of 4 years of experience in medical review, or experience in an applicable pharmaceutical-industry role with strong knowledge of global regulatory requirements, is preferred.
  • Strong scientific, clinical, and analytical knowledge to assess individual case safety reports and understand their safety and medical implications.
  • Exceptional communication, collaboration, and project management skills.
  • High attention to detail, scientific rigor, and a proactive, solutions-oriented mindset.

Responsibilities

  • Establish recognition as an expert on medical safety assessment of individual cases and line listings.
  • Perform peer retrospective medical review quality control activities.
  • Respond to medical review-related questions from other functions in a timely manner.
  • Collaborate with global safety leads and global safety strategy leads to assess and communicate suspected unexpected, serious adverse reactions (SUSARs) reports from clinical trials.
  • Provide medical consultation to Patient Safety Strategic Operations functional groups, including Literature Management, Coding Strategy, and Auto Labeling Management, on an ad hoc basis.
  • Contribute significantly to the ongoing development and refinement of medical review processes, standards, practices, efficiencies, and capabilities.
  • Lead or contribute to developing and maintaining procedural documents for medical review activities and provide training.
  • Support internal and external audits and inspections.
  • Participate in internal and external educational initiatives.
  • Contribute to process improvement within Patient Safety, particularly in adverse event processing and operational aspects.
  • Initiate, lead, or contribute to functional or cross-functional projects.
  • Ensure own work complies with established practices, policies, processes, and regulatory or other requirements.
  • Provide mentorship and train junior staff, new hires, and contractors to independently review adverse event reports for investigational and marketed products.
  • Create inclusion by recognizing the business value of diverse teams, modeling inclusion, and embedding diversity in how teams are managed.
  • Develop talent by understanding employees’ skills, experience, aspirations, and potential, coaching them on performance and future potential, and ensuring they receive feedback and insight to grow and develop.
  • Empower teams by aligning goals, purpose, and organizational objectives, holding teams accountable, removing barriers, and connecting them to the broader organization.

Desired Qualifications

  • Board certification is preferred.

About the Company

Gilead Sciences

Makes medicines for HIV, liver disease and cancer

Gilead Sciences is a biopharmaceutical company that discovers, develops and sells medicines for HIV, viral hepatitis and other liver diseases, cancer and inflammatory conditions. Its HIV business covers both treatment, led by the once-daily pill Biktarvy, and prevention, including Descovy and Yeztugo, a lenacapavir injection given twice a year. In cancer, its Kite unit makes CAR T-cell therapies from patients' own immune cells, and Trodelvy is an antibody-drug conjugate for breast cancer. Gilead earns revenue by selling its drugs to wholesalers, specialty pharmacies, hospitals and governments worldwide after regulatory approval. The company was founded in 1987 and is headquartered in Foster City, California.

Company size
10,001+
Company stage
IPO
Headquarters
Foster City, CA
Founded
1987

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