Exelixis Jobs in United States

Job Purpose · In collaboration with Exelixis clinical teams, this Clinical Development Medical Director leads and executes early/late stage clinical trials for oncology products in development. · Designs protocols and other required documentation in compliance with project plans. ...

The Senior Clinical Trials Specialist coordinates the activities associated with the evaluation, initiation, and management of oncology clinical trials.Provides operational support to the Study Delivery Lead (SDL) by managing assigned study activities and clinical sites. · ...

Responsible for all aspects of Clinical Trial data management from study start-up through database lock and study closure to ensure optimized data collection, ensuring the accuracy and consistency of data for analysis and reporting. · ...

The position will be an integral part of the Corporate Legal Affairs team with respect to all aspects of its securities and corporate governance practice. · Develop and maintain standardized workflow checklists and calendaring system relating to SEC rules and processes. · ...

The Director leads a team responsible for analytical activities at external contract development and manufacturing organization (CDMO) sites to support the development and manufacturing of biological drug candidates. The incumbent utilizes technical expertise to advance CMC devel ...

The Senior Director, Sales - Regional provides strategic leadership and vision across multiple geographic territories, ensuring alignment with national and global commercial priorities. · This role drives sustainable revenue growth, market penetration, and competitive positioning ...

This Associate Director is accountable for driving a risk based comprehensive implementation of the DI program meeting cGxP regulations and responsible for Computer System Validation oversight by setting and maintaining a company strategy QA oversight evaluating CSV regulatory la ...

The Associate Director - CRC Key Customer Strategy is responsible for supporting brand strategy development and execution for zanza's initial launch and ongoing promotion in metastatic colorectal cancer (mCRC). · ...

this role is responsible for providing drug safety expertise and ensuring the quality documentation of safety data particularly serious adverse events saes this role provides support for all major tasks and oversight of outsourced vendors related to the management and best utiliz ...

Job summary The Associate Compliance QA Director - Vendors is responsible for QA oversight of the end-to-end vendor management program . Develops and maintains the approved vendor list , applies quality risk management ( QRM ) and phase-based approach . Represents QA as the QA P ...

+The Clinical Pharmacology Associate II supports the clinical pharmacology and DMPK functions in pharmacokinetics (PK) data assembly, calculation, analysis, review, and documentation in addition to contributing to the multidisciplinary development teams by facilitating designing ...

The Senior DMPK Director has strong scientific, technical and leadership skills to develop and implement DMPK and modeling & simulation strategies. · Lead the Translational IND- and NDA-enabling ADME work; · Analyze and interpret preclinical pharmacokinetic... · ...

The incumbent will be responsible for the day-to-day execution activities directed to support development and manufacturing of biological drug products. The activities include formulation development DP manufacturing process development technical transfer preparation and administ ...

Job Overview · The Director, Cloud Engineering will lead a portfolio of cloud products critical to Exelixis's success.This individual will define product roadmaps, foster cross-functional collaboration, and lead agile product teams to deliver innovative solutions. · Define AWS la ...

Job Description: · The Corporate Legal Affairs team manages all aspects of its securities and corporate governance practice. · This includes managing corporate legal records, supporting SEC filings, contracts, business transactions, employment and investor relations matters as as ...

Senior Staff IT Product Lead · This role leads a portfolio of digital products critical to Exelixis's success and ambition to launch innovative medicines for patients. · Define product roadmaps, foster cross-functional collaboration, and lead agile product teams to deliver innova ...

SUMMARY/JOB PURPOSE: · The Bioanalysis Director (BD) will manage outsourced regulated bioanalytical work for small molecules with LC-MS/MS in support of pharmacokinetic (PK) for nonclinical and clinical studies. They will possess strong technical expertise with LC-MSMS bioanalysi ...

SUMMARY/JOB PURPOSE: · The Senior Manager provides technical leadership and support across multiple CMC biologics areas to drive technology transfer process validation manufacturing biological drug candidates focus Biologics mAbs Bi-specifics Antibody Drug Conjugates ADCs. · Appl ...

HR Business Partnership · The organization seeks a seasoned HR expert to partner with leaders across departments. · Serves as a strategic advisor to management teams regarding organizational development and change management initiatives. · ...

A leading biotech company in Alameda, California, is seeking an Assoc Scientific Regulatory Writing Director to lead the development of regulatory documents. This role requires extensive experience in the biotech/pharmaceutical industry and a strong understanding of regulatory su ...