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Exelixis

Biopharmaceutical oncology company developing cancer therapies

Associate Clinical Operations Compliance Director - Biotechnology, Oncology

Clinical Research OperationsUpdated on Nov 10
Full-timeRemote in USA

About the Job

Requirements

  • A bachelor's degree in a related discipline and at least 11 years of related experience, or a master's degree in a related discipline and at least 9 years of related experience, or a doctoral degree in a related discipline and at least 5 years of related experience, or an equivalent combination of education and experience.
  • Experience in the biotechnology or pharmaceutical industry.
  • A current understanding of the relevant external scientific, legal, and regulatory environment.
  • Strong knowledge of biopharmaceutical industry regulations, standards, and best practices.
  • The ability to work independently with minimal supervision.
  • Strong analytical, strategic thinking, problem-solving, time management, change management, and organizational skills, including the ability to work in a fast-paced environment and adapt to changing business plans and priorities.
  • Strong interpersonal, verbal, and written communication skills.
  • Strong attention to detail.
  • The ability to identify and communicate issues and risks.
  • Presentation skills.
  • The ability to build and maintain strong relationships.
  • The ability to influence without direct authority.
  • Advanced knowledge of Microsoft Excel, Word, PowerPoint, and Outlook.

Responsibilities

  • Support the risk and issue management process for Clinical Operations, focusing on compliant delivery of study execution.
  • Contribute to strategy and methodology for functional risk and issue management, assist in creating the annual functional risk management plan to ensure inspection readiness, collaborate cross-functionally on risk management activities, escalate issues to appropriate governance, and adapt accordingly.
  • Support Clinical Operations and other functions being supported by the embedded compliance role, including CAPA owners, owner assignment, follow-up, and completion.
  • Assist with updates on CAPA completion data, including late, near-due, and due-later items.
  • Act as a liaison for the Quality Assurance team and other functional teams across R&D and beyond.
  • In one or more assigned areas, build standardized GCP and process training curricula, drive ongoing capability and knowledge sharing, and build and renew quality metrics to track progress and consistency across Clinical Operations.
  • In one or more assigned areas, drive continuous inspection readiness across studies, keep the TMF audit-ready, run mock inspections and CAPA follow-up, and lead BIMO and health authority inspection responses.
  • In one or more assigned areas, oversee monitoring quality and CRO performance, review risk-based monitoring signals, and ensure timely escalation of site and data issues.
  • Perform other duties as assigned.
  • Comply with all policies and standards.

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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