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Summary The Clinical Trial Manager (CTM) will provide clinical study support to the Clinical Program Manager/Study Management Team Lead (SMTL) for one or more clinical studies, ensuring efficient delivery of clinical trials in a matrix environment. Key accountabilities include assuring successful co

Summary The Senior Manager, Clinical Quality Assurance is responsible for working with study management teams to facilitate internal and external adherence to Quality and Regulatory Compliance by ensuring conformance to domestic and international quality regulations and GCP guidelines. The role is a

Summary The Senior Manager, Records Management (SMRM), will be responsible for leading activities to support major initiatives across the Records Management Organization. The SMRM will provide leadership and oversight of Trial Master File (TMF) operations, enhancing functionality, efficiency, scalab

Summary The Associate Director, Outsourcing and Vendor Governance will play a key role in leading the Vendor Governance function and supporting clinical outsourcing activities for current and future clinical trials. This position is responsible for driving effective vendor governance while also supp

Summary The Associate Director, Medical Affairs – Publications - Contractor will be an essential leader and responsible for driving the publications strategy and activities across the Arcus portfolio. The individual will lead the publications process and play an integral role in driving strategy dev

Summary The Manager, Safety Quality and Compliance - Contractor will be responsible for supporting the development, management and oversight of processes, systems and PV inspection preparedness activities pertaining to safety and pharmacovigilance to ensure PV compliance with global regulations. Thi

Summary The Senior Clinical Program Manager (Sr. CPM) is responsible for the strategic and operational leadership of one or more complex clinical studies. This role ensures clinical trials are executed on time, within budget, and in compliance with ICH GCP, regulatory requirements, and Arcus SOPs. T

Arcus Biosciences is seeking an experienced Senior Manager, IT Qualification & Validation to join our dynamic and collaborative team. This is an opportunity to make a meaningful difference in a growing, fast-paced, clinical-stage organization. In this role, you will provide senior-level leadership a

Summary The Sr. Clinical Trial Manager (CTM) will provide clinical study support to the Clinical Program Manager/Study Management Team Lead (SMTL) for one or more clinical studies, ensuring efficient delivery of clinical trials in a matrix environment. Key accountabilities include assuring successfu

Summary The Specialist, Biosample Operations Contractor will assist Biosample Managers in planning, implementing, managing, and driving biological sample logistics across Phase I-IV Clinical Trials. This role is an essential member of the Clinical Operations function and must be able to collaborate

We currently have an opportunity for a Research Associate Contractor to join our Lead Discovery and Optimization group. The Lead Discovery and Optimization group is central to the assessment and selection of drug candidates and the advancement of research programs into clinical evaluation.We are loo

The Manager of Patient Safety and Pharmacovigilance (PV) Operations Contractor will be responsible for supporting the development, management, and oversight of end-to-end safety case processing and safety reporting activities performed by the external safety vendor and multiple CROs. The candidate w

Summary The Senior Statistical Programmer Analyst Contractor will be responsible for supporting the submission readiness of study data packages per CDISC standards and FDA guidance, planning, execution, and quality of statistical analyses, and statistical programming infrastructure. This position wi

Summary The Senior Clinical Programmer Contractor will be responsible for support of team data review, data reconciliation and edit checks, and programming submission ready SDTM deliverables. This position will report to a Senior Manager of Clinical Programming or higher and will interact regularly

Summary The Clinical Trial Manager - Contractor (CTM) will provide clinical study support to the Clinical Program Manager/Study Management Team Lead (SMTL) for one or more clinical studies, ensuring efficient delivery of clinical trials in a matrix environment. Key accountabilities include assuring

Summary The Senior Clinical Scientist will be a contributor to the scientific, clinical, and operational scope of clinical development programs with an emphasis on protocol-specific activities. The Senior/ Principal Clinical Scientist will help drive the planning and implementation of study protocol

Summary The Sr. Scientist will provide hands-on formulation and process expertise primarily in solid oral formulations related activities and present scientific data in the drug product development function. Responsibilities Provide hands-on formulation and process expertise to develop clinical and

At Arcus, the Director, Clinical Pharmacology (CP) functions as the Clinical Pharmacology (CP) team representative at the project teams for small molecule and biotherapeutics in Phase 1-3 of clinical development and is responsible for supporting all clinical pharmacology-related activities. This inc

SummaryThe Biology department is seeking a self-motivated, knowledgeable, and technically skilled immunologist with a deep understanding of inflammatory and autoimmune disease mechanisms. In this role, you will design, execute, and interpret experimental studies to demonstrate the mechanism of actio

Summary The Associate Director, Clinical Science will be a key contributor to the scientific, clinical, and operational scope of clinical development programs in both inflammation/immunology and oncology, with an emphasis on program-specific activities. The Associate Director, Clinical Science will