Arcus Biosciences Jobs in United States

This position is responsible for collecting and maintaining essential Regulatory documents for the Trial Master File (TMF) in accordance with Good Clinical Practice (GCP), E6 ICH Guidelines and other regulatory guidance documents. · Work directly with TMF Content Owners to identi ...

This position is responsible for collecting, reviewing, maintaining and archiving essential regulatory documents for the Trial Master File (TMF) in accordance with Good Clinical Practice (GCP), E6 ICH Guidelines and other regulatory guidance documents. The Senior Clinical Documen ...

This position is responsible for collecting, reviewing, maintaining, and archiving essential Regulatory documents for the Trial Master File (TMF) in accordance with Good Clinical Practice (GCP), E6 ICH Guidelines and other regulatory guidance documents, relevant regulations (e.g. ...

The Principal Investigator-Nonclinical Safety Assessment will function as a project toxicologist in providing scientific expertise in support of programs from discovery through both early and late phases of clinical development. · Work directly with the Nonclinical Safety team in ...

Description · Summary · The Clinical Operations Line Manager is responsible for the recruitment, development, and leadership of Clinical Operations staff, including Clinical Program Managers, Clinical Trial Managers and Clinical Trial Associates. This role ensures high-quality ex ...

· Description · Summary · The Clinical Operations Line Manager is responsible for the recruitment, development, and leadership of Clinical Operations staff, including Clinical Program Managers, Clinical Trial Managers and Clinical Trial Associates. This role ensures high-qualit ...

· Summary · The Clinical Operations Line Manager is responsible for the recruitment, development, and leadership of Clinical Operations staff, including Clinical Program Managers, Clinical Trial Managers and Clinical Trial Associates. This role ensures high-quality execution of ...

Description · This position is responsible for collecting, reviewing, maintaining, and archiving essential Regulatory documents for the Trial Master File (TMF) in accordance with Good Clinical Practice (GCP), E6 ICH Guidelines and other regulatory guidance documents, relevant reg ...

· This position is responsible for collecting, reviewing, maintaining, and archiving essential Regulatory documents for the Trial Master File (TMF) in accordance with Good Clinical Practice (GCP), E6 ICH Guidelines and other regulatory guidance documents, relevant regulations (e ...

This position is responsible for collecting and maintaining essential Regulatory documents for the Trial Master File (TMF) in accordance with Good Clinical Practice (GCP), E6 ICH Guidelines and other regulatory guidance documents. · ...

The Associate Director 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 ...

This position is responsible for collecting, reviewing, maintaining, · and archiving essential Regulatory documents for the Trial Master File (TMF) in accordance with Good Clinical Practice (GCP), E6 ICH Guidelines and other regulatory guidance documents, · relevant regulations ( ...

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 infrastruc ...

The Pharmacology Department at Arcus Biosciences is seeking a motivated summer intern to join our In Vivo Pharmacology group. · The intern will assist in designing pharmacology studies in accordance with institutional guidelines.Responsibilities include administering compounds to ...

The Drug Metabolism and Pharmacokinetics (DMPK) department plays a key role in Arcus' R&D by characterizing the ADME properties of drug candidates and providing data-driven insights to drug discovery and development. · Develop and optimize high-throughput LC-MS methods using seru ...

As Senior Director of Regulatory Affairs at Arcus Biosciences in South San Francisco, USA you will provide regulatory leadership and develop strategies to support clinical trial applications and marketing approvals. · Key Responsibilities: · Provide strong regulatory and scientif ...

+This position is responsible for collecting and maintaining essential Regulatory documents for the Trial Master File (TMF) · +• Work directly with TMF Content Owners to identify issues · • Review and classify documents collected from internal and external sources · • Reconcile e ...

This position is responsible for collecting reviewing maintaining and archiving essential regulatory documents for the Trial Master File TMF in accordance with Good Clinical Practice GCP E6 ICH Guidelines and other regulatory guidance documents relevant regulations e.g. 21 CFR Pa ...

· Summary · The Clinical Operations Line Manager is responsible for the recruitment, development, and leadership of Clinical Operations staff, including Clinical Program Managers, Clinical Trial Managers and Clinical Trial Associates. This role ensures high-quality execution of ...

This role will support the development of Arcus Quality Assurance inspection readiness programs. · Participate in the development, implementation and continuous improvement of inspection readiness processes... · ...