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. · ...

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 ...

Arcus is seeking a highly motivated individual to join our Drug Metabolism and Pharmacokinetics team for a summer internship. · Gain hands-on experience with ADME computational modeling in a pharmaceutical R&D setting · Integrate ADME computational models into interactive web app ...

The Lead Discovery and Optimization group is central to the assessment and selection of drug candidates · A minimum of one year college education. · Scientific laboratory experience preferred. · ...

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) guidelines. · Responsibilities including but not limited to:Work directly with TMF Cont ...

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... · ...

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 ...

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 ...

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 ( ...

Job Description · The Lead Discovery and Optimization group is central to assessing drug candidates and advancing research programs into clinical evaluation. · This internship provides hands-on experience with laboratory techniques/assay application in drug discovery settings. · ...

+Job summary · The Director , Medical Writing (MW) responsible managing MW quality review activities in conjunction Head of MW timely accurate efficient manner in compliance company global regulations. · +ResponsibilitiesEnsure appropriate communication project program-related ma ...

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 ...

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. · ...

Arcus Biosciences' Small Molecule Drug Substance Development and Manufacturing group plays a key role of developing efficient synthetic chemical processes for the manufacturing of active pharmaceutical ingredients (APIs or Drug Substances). · ...

The Associate Director of Clinical Cost Analytics manages clinical program and clinical trial cost modeling forecasts benchmarking metrics and general business analytics to demonstrate cost optimization savings and return on investmentPerform project management for assigned initi ...

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 ...

The Senior Director of Regulatory Affairs provides regulatory leadership and develops regulatory strategies for products in development to support clinical trial application and marketing approvals in the US and internationally. · Provides strong regulatory and scientific leaders ...

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 ...

We are seeking a motivated and dynamic intern this coming summer to lead a high-impact project focused on driving substantial business process and/or technology improvements within our global supply chain organization. · This opportunity presents a unique chance to help ensure d ...

Lead Discovery Pharmacology Intern · This internship offers hands-on experience in laboratory techniques, assay development, and data analysis in a fast-paced research environment. · Work with tissue culture using aseptic techniques · Safely operate robotic workflows and automat ...