The QA Associate supports QA Partner in managing GxP supplier quality activities, including vendor qualification, audit preparation, records management, and maintaining relationships with stakeholders. Responsibilities include maintaining audit-related information, supporting inspection readiness, compiling vendor risk assessments, and tracking quality metrics.

The Senior Workday Technology Manager will lead the development and operations of HR technology, ensuring high-quality delivery of integrations, reports, and features in Workday. They will collaborate with teams to enhance user experience, manage the testing process, and drive continual service improvement focused on HR priorities.

The Senior QA GCP Manager is responsible for developing and maintaining QA systems, conducting audits, managing compliance metrics, training staff, and providing regulatory support. They oversee GCP and PV activities, partner with clinical teams, and ensure adherence to regulatory standards, while also managing complex issues and compliance challenges.

As a Senior Staff Engineer in Cybersecurity Operations, you will lead the threat management process, develop incident response plans, enhance threat detection capabilities, conduct threat hunting exercises, and mentor junior analysts. You'll work collaboratively across teams to protect critical assets and ensure compliance with industry standards.

The Senior Director of Zanzalintinib Marketing will oversee the commercialization and launch strategy of the pharmaceutical product Zanzalintinib. Responsibilities include market research, developing promotional content, engaging with key stakeholders, managing vendor relationships, and ensuring compliance with regulations. The role requires significant experience in pharmaceutical marketing and oncology.

The Director of Strategic Sourcing & Procurement will lead the Research Category, managing procurement strategies, vendor relationships, and operational oversight. They will work closely with business leaders to optimize spend and enhance vendor partnerships, ensuring alignment with business objectives and compliance with regulations.

Exelixis is seeking an Associate Corporate Counsel to join the Legal Department’s corporate team. The role involves assisting with SEC public reporting, supporting corporate governance, providing legal advice on securities matters, and overseeing various legal activities within the organization.

The Associate Corporate Counsel will provide transactional legal support primarily in drafting, reviewing, and negotiating contracts for Research and Development departments. Responsibilities include advising on legal risks, facilitating communications among stakeholders, and contributing to the creation of business solutions under the supervision of senior legal counsel.

The Associate Statistical Programming Director oversees the programming team, ensuring the implementation of CDISC standards and the quality of statistical programming. They develop tools for data integrity, mentor staff, manage performance, and communicate with other departments to meet regulatory requirements and support clinical trials.

The Learning Experience Program Manager will oversee various learning initiatives, manage the learning platform, assess training needs, create engaging content, and evaluate the effectiveness of programs. Responsibilities include stakeholder communication, budget tracking, operational management, and providing career development support.

The Associate Director of Analytical Development leads the in-house Analytical Development group, overseeing the development and validation of analytical methods for investigational drugs. Responsibilities include managing internal and contract lab activities, contributing to project development plans, supervising a team, and ensuring compliance with regulatory requirements.

The Biostatistics Director leads the statistical strategy for clinical trials across all phases, ensuring compliance with health authority guidelines and regulatory requirements. They are responsible for statistical design, analysis, and providing strategic guidance while managing study timelines, deliverables, and budgets, mainly interacting with regulatory agencies. This role demands a deep understanding of statistical methods applied to clinical research, particularly in oncology.

The Associate Corporate Counsel will draft, negotiate, and manage a variety of contracts focusing on IT and related services. Responsibilities include advising on existing agreements, communicating risks, liaising with internal clients, and ensuring contracts protect Exelixis' interests. The role requires collaboration on templates and playbooks to improve contracting processes.

The Senior Human Resources Business Partner will act as a strategic partner to organizational leaders, improving HR elements, managing complex employee relations issues, and ensuring compliance with legal requirements. Responsibilities include advising on HR practices, developing human capital strategies, leading HR projects, and mentoring HR partners.

The Senior Corporate Counsel will manage a legal team, ensuring compliance with SEC and Nasdaq regulations, handling corporate governance and public disclosures, and supporting corporate development transactions. Responsibilities include drafting legal agreements, managing corporate structure, and collaborating with various departments and external counsel.

The Senior Corporate Counsel, Commercial provides legal support for the Commercial Department at Exelixis, focusing on regulatory and transactional advice. Responsibilities include drafting and negotiating contracts, ensuring compliance with regulations, advising on government pricing, and maintaining company policies. The role requires collaboration with various departments and oversight of legal compliance processes.

Lead statistical programming activities at the project level using SAS. Responsible for creating and maintaining statistical software programs, datasets, and ensuring quality control of data analysis. Collaborate with biostatisticians and clinical data management to establish clinical data standards and adhere to regulatory guidelines. Oversee development of datasets in SDTM and provide training on macros and programming conventions.

The Senior Director & Counsel will lead the G&A Contracts team, focusing on drafting and negotiating various contracts, managing legal risks, and advising on agreements. The role involves overseeing contracts related to IT, data privacy, and other administrative functions, while also developing policies and supervising attorneys and contract managers.

The Bioanalysis Director will manage GxP-compliance in bioanalytical work for clinical studies, oversee CRO-outsourced bioanalysis, and ensure project quality and timely delivery. Responsibilities include managing lab operations, interacting with quality assurance teams, authoring SOPs, and contributing to regulatory filings. Supervision of 1-2 direct reports is included.

The Senior Director of Biostatistics will lead the biostatistics function, managing staff and overseeing statistical strategy for early phase clinical trials. This role involves developing and applying statistical theories, managing timelines and budgets with contract research organizations, and providing guidance on clinical biomarker strategies. The director will ensure compliance with regulatory requirements and foster collaboration within the department and external stakeholders.