Principal Clinical Scientist (Office or Remote)

$195,000 - $205,000/Yr

Arcus Biosciences - Hayward, CA

Full-time - Senior

Remote - Hayward, CA

Professional, Scientific, and Technical Services

About the position

The Principal Clinical Scientist will play a crucial role in the scientific, clinical, and operational aspects of clinical development programs, focusing on protocol-specific activities. This position involves designing, planning, and implementing study protocols for investigational products, supporting regulatory activities, and collaborating with cross-functional teams to ensure the successful execution of clinical trials. The role also includes data interpretation and communication with stakeholders, as well as contributing to internal process improvements within the clinical department.

Responsibilities

• Partner with cross-functional teams to conduct clinical studies, including operational feasibility and data management deliverables.
• Support senior team members with medical monitoring reports, safety reviews, and site interactions.
• Provide analytical support for clinical trial data, including gathering, analyzing, and interpreting data.
• Assist in communicating a clear overview of trial results.
• Provide organizational support for Data Monitoring Committees and Safety Review Committees.
• Author protocols and contribute to clinical study reports and other regulatory documents.
• Interact with internal and external stakeholders to support clinical trial objectives.
• Act as a recognized clinical expert for assigned studies.
• Write and review collaborative abstracts and content for scientific meetings.
• Support publication strategy execution and present at investigator meetings.

Requirements

• PhD degree in health science field, PharmD, MD or equivalent advanced degree.
• At least 5+ years of experience as a clinical scientist or in a related role in a pharmaceutical, CRO, or biotechnology company.
• Experience in oncology or oncology immunotherapy clinical trials preferred.
• Strong data analysis and interpretation skills, with an understanding of safety and pharmacovigilance principles.
• Working knowledge of biostatistics, GCP, and regulatory requirements for clinical studies.
• Excellent interpersonal, verbal, and written communication skills.

Nice-to-haves

• Experience with clinical trial design and execution.
• Familiarity with regulatory submissions and compliance processes.

Benefits

• Competitive salary range of $195,000 - $205,000 annually.
• Participation in stock programs.
• Performance-based bonus.
• Comprehensive benefits package.