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Exelixis

Biopharmaceutical oncology company developing cancer therapies

Drug Safety Associate 3

Regulatory & Quality (Life Sciences)Updated on Nov 10
Full-timeRemote in USARemote

About the Job

Requirements

  • A BS/BA degree in Nursing, Pharmacy, another clinical discipline, or a related discipline and at least 7 years of related experience; alternatively, an MS/MA degree in those fields and at least 5 years of related experience; a PhD in those fields with 0 or more years of related experience; or an equivalent combination of education and experience.
  • May require certification in the assigned area.
  • Experience processing clinical-trial and spontaneous adverse events.
  • Knowledge of the biotechnology or pharmaceutical sector and the regulatory framework governing patient safety.
  • Use an analytical approach to solve problems relevant to the role.
  • Manage personal time and resources to complete assigned work.
  • Communicate clearly in writing and verbally, keep management informed of potential issues in a timely manner, and collaborate with team members.
  • Apply interpersonal skills to understand differing views and help develop agreed-upon resolutions.
  • Follow predefined procedures, identify task-related challenges, prioritize work, escalate issues with broader impact, and implement solutions.

Responsibilities

  • Process and assess serious adverse events from receipt through case closure in the Argus database, including query generation, narratives, and adverse event summaries.
  • Code serious adverse events and adverse events in MedDRA based on source documents, and develop or revise MedDRA coding conventions to ensure consistent categorization.
  • Conduct case quality reviews to ensure sound medical safety data documentation, with support from the Drug Safety Physician.
  • Schedule expedited safety report submissions in Argus as needed.
  • Train new safety staff on Argus and case processing.
  • Collaborate with Clinical Development, Clinical Operations, Data Management, Regulatory Affairs, and Project Management to ensure appropriate collection and handling of safety data.
  • Perform Safety Study Lead activities, including reviewing Investigator Brochures and study protocols and participating in IND Annual Reports in support of the Drug Safety Physician.
  • Develop study-specific safety management plans using the Drug Safety template.
  • Develop, review, and update drug safety forms and templates, and harmonize them with relevant clinical operations forms and templates, including SAE data collection forms and CRFs.
  • Perform SAE reconciliation as required by the safety management plan.
  • Complete additional duties and responsibilities as required.
  • Manage and execute assigned work to contribute to departmental goals.
  • Train on procedures, tasks, and tools for the role, supported by ongoing coaching or mentoring from departmental peers.
  • Develop and maintain knowledge of cross-functional products, tools, and data sources; may mentor junior team members.

Desired Qualifications

  • Experience in the biotechnology or pharmaceutical industry and/or in oncology.
  • Experience using the Argus safety database.

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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