Clinical Development Jobs in Alameda, CA

Summary/Job Purpose (Basic purpose of the job):The Senior DMPK Director has strong scientific technical and leadership skills to develop and implement DMPK and modeling & simulation strategies to advance drug candidates from discovery to development stage and build comprehensive DMPK packages to ena...

SUMMARY/JOB PURPOSE (Basic purpose of the job):The position will be accountable for contributing to cross-functional initiatives to advance the development of Zanzalintinib Exelixis oral multi-TKI in late-phase development. This position will provide critical information and advice to Exelixis leade...

SUMMARY/JOB PURPOSE:The role of Exelixis Business Development Search & Evaluation (BD S&E) team is to establish and manage a highly productive agile global business opportunity identification network. Key objectives include building broad awareness of Exelixis partnering goals building a first-to-ca...

SUMMARY/JOB PURPOSE: The Clinical Data Management (CDM) Director is a highly experienced and influential leader with expert knowledge of Clinical Data Management concepts and processes. This position is accountable for the operational leadership of CDM activities across all solid tumor oncology clin...

SUMMARY/JOB PURPOSE:The Senior Clinical Trials Manager Clinical Operations combines end-to-end design execution and reporting of oncology clinical trials with leadership in study teams and across matrix teams. This position within Clinical Operations is accountable for planning and leading the deliv...

SUMMARY/JOB PURPOSE:Provides leadership within biostatistics function to develop and execute statistical strategy design and analyses for clinical trials in all phases. Applies sound statistical methodology to meet project objectives health authority guidelines and regulatory requirements. Develops...

SUMMARY/JOB PURPOSE (Basic purpose of the job):The Senior Director Clinical Operations Compliance Management (COCM) is responsible for ensuring that clinical research activities are conducted by clinical staff in accordance with ICH GCP relevant international and local regulations requirements and g...

SUMMARY/JOB PURPOSE: The Senior Staff IT Product Lead - Digital Applications will lead a portfolio of digital products critical to Exelixiss success and ambition to launch innovative medicines for patients. This role is pivotal in driving the strategy development and operational excellence of our di...

SUMMARY/JOB PURPOSE: Provides leadership to the biostatistics function and direct management of biostatistics staff in developing statistical strategy design and analyses for clinical trials for multiple compounds with a focus on early phase (1/2) trials. Sets direction for statistical support of tr...

SUMMARY/JOB PURPOSEThis 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 util...

SUMMARY/JOB PURPOSEThe Associate QA Operations Director Labeling & Systems is accountable for providing QA lead support for Quality Systems (Deviations Change Control CAPA etc.) As a Partner responsible for guiding the organization in the successful thorough and timely execution of complex Quality...

SUMMARY/JOB PURPOSEThe Associate QA Operations Director Systems and Process is accountable for providing QA lead support for Quality Systems (Deviations Change Control CAPA etc.) As a Partner responsible for guiding the organization in the successful thorough and timely execution of complex Quality...

COMPANY DESCRIPTION:Every Exelixis employee is united in an ambitious cause: to launch innovative medicines that give patients and their families hope for the this pursuit we know our employees are our most valuable asset. After operating in the challenging biotech sector for 25 years we have a pro...

SUMMARY/JOB PURPOSE (Basic purpose of the job):The Compliance QA Director leads the companys GxP inspection readiness ensuring ongoing preparedness for global health authority inspections. This role manages regulatory inspections and responses directs internal audits and mock inspections and provide...

SUMMARY/JOB PURPOSE: The Executive Medical Director PVRM is responsible for the development and execution of the global product safety strategy for complex clinical development program(s) as well as post-marketing pharmacovigilance activities for Exelixis products. This role leads and mentors team m...

SUMMARY/JOB PURPOSE:This key role drives consistency across QA systems and processes for the Clinical QA team identifying issues and risks escalating in a timely fashion and aligning metrics that provide input into a compliance scorecard for Clinical programs. This leader provides insight and partne...

The GCP/GVP QA Director is accountable for Good Clinical Practices (GCP) and Good Pharmacovigilance Practices (GVP) systems and activities drives compliance and continuous improvement ensures that Quality is integrated throughout GCP/GVP processes supports internal/external audits implements Quality...

SUMMARY/JOB PURPOSE (Basic purpose of the job):The Senior GCP/GVP QA Manager is accountable for assisting with the development implementation and maintenance of end-to-end QA systems and activities for GCP/GLP operations including planning and supporting vendor audits and associated documentation ac...

Job TitleClinical Development ScientistJob DescriptionClinical Development Scientist Image Guided Therapy DevicesThe Clinical Development Scientist ensures clinical trial protocols and studies comply with regulatory standards and business strategies producing thorough evaluation reports and regulato...