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Exelixis

Biopharmaceutical oncology company developing cancer therapies

Executive Medical Director - Pharmacovigilance Risk Management

Biology & BiotechUpdated on Nov 10
Full-timeRemote in USA

About the Job

Requirements

  • An M.D. degree and a minimum of 10 years of post-residency experience, or an equivalent combination of education and experience.
  • At least 3 years of clinical experience post-residency.
  • At least 10 years of pharmacovigilance or other relevant experience, such as clinical research, in a pharmaceutical or biotechnology company; significant clinical experience may compensate for shorter pharmaceutical or biotechnology company experience.
  • Solid knowledge and understanding of United States and European Union pharmacovigilance regulatory requirements and general regulatory expectations.
  • Extensive knowledge of biotechnology and pharmaceutical sector drivers and practices throughout the product lifecycle.
  • Extensive knowledge of United States and international pharmacovigilance regulations, with experience applying them throughout the product lifecycle.
  • Ability to gather, analyze, and apply key information to solve complex problems.
  • Organizational and planning capabilities, including managing a function’s time, workload, and resources.
  • Ability to lead and manage a functional area within a department to execute team objectives that contribute to functional and departmental goals.
  • Verbal and written communication skills, including selecting appropriate methods and media, communicating clearly in one-to-one settings, and presenting effectively to large audiences inside and outside the company.
  • Interpersonal skills and ability to incorporate differing views to resolve challenges and develop agreed-upon resolutions.
  • Ability to develop procedures, tasks, and tools; train staff on departmental products, tools, and data sources; maintain knowledge of cross-functional products, tools, and data sources; mentor junior team members; and contribute to team members’ performance reviews and professional development plans.
  • Ability to strategically and proactively assess workload, trends, tasks, and priorities for cross-functional activity.
  • Ability to plan and execute multiple projects or activities, consider alternatives and contingency plans, avoid potential issues, and promote efficiency.
  • Ability to design and implement solutions to cross-functional challenges while considering broader impacts.

Responsibilities

  • Develop and execute global product safety strategy for complex clinical development programs and post-marketing pharmacovigilance activities.
  • Lead and develop safety strategy for complex clinical development programs for oncology products in development or products with marketing authorization.
  • Create safety data analysis strategies across clinical studies for a product.
  • Interpret safety analysis data for a product.
  • Set strategy for key product safety deliverables, including safety signals, aggregate reports, risk management planning, safety data pooling, regulatory filing documents, and clinical development documents.
  • Lead the cross-functional Benefit Risk Team for an assigned product and escalate important safety updates to the Benefit Risk Executive Committee in a timely manner.
  • Lead development of core safety documents that appropriately characterize the product’s safety profile.
  • Lead proactive safety data reviews and anticipate safety concerns for an assigned product.
  • Oversee development of safety data evaluations and summaries in global periodic safety aggregate reports for a product.
  • Present safety data and provide product safety expertise in meetings with health authorities, Data Safety Monitoring Boards, and investigators.
  • Develop risk management strategies and monitoring plans to assess risk management effectiveness for a product.
  • Co-lead product benefit-risk assessment with other functions.
  • Supervise direct reports.
  • Collaborate with clinical development, biometrics, medical affairs, and regulatory affairs in a matrix environment.
  • Manage time, workload, and resources of a function and execute functional objectives contributing to departmental goals.

Desired Qualifications

  • Board certification, if practicing in the United States.
  • Pharmacovigilance experience in oncology.
  • Prior project and team leadership or management experience.

About the Company

Exelixis

Biopharmaceutical oncology company developing cancer therapies

Exelixis develops and commercializes medicines for cancer. Its products aim to treat advanced cancers, including renal cell carcinoma, by targeting multiple biological pathways and supporting combination regimens to achieve effective, tolerable, and durable responses. The company generates revenue from sales of approved therapies and strategic partnerships, backed by extensive research, clinical trials, and regulatory approvals to bring new drugs to market. Compared with peers, Exelixis focuses on a pipeline that combines multi-pathway targeting with combination therapies to improve patient outcomes. Its overall goal is to advance cancer treatment and offer patients better chances of remission through its ongoing drug development programs.

Company size
1,001-5,000
Company stage
IPO
Headquarters
San Francisco, CA
Founded
1994

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