Arcus Biosciences is hiring: Clinical Scientist in hayward

Responsibilities: Conduct cross-functional clinical studies, including feasibility, data management deliverables, meeting materials, communication plans, safety monitoring, status updates, and study close-out activities Support medical monitoring reports, safety reviews, site interactions, and review of TFLs Provide analytical support for trial data (safety and efficacy) including data gathering, analysis, interpretation, and preliminary recommendations Assess issues related to protocol conduct and subject safety Assist in communicating trial results clearly Support Data Monitoring Committees and other data review committees (charters, data updates, meetings, adjudications, data reports) Contribute to authorship of study protocols, clinical study reports, IBs, ICFs, training documents, and other clinical/regulatory documents Interact with study sites, vendors, and committees to support trial objectives Conduct literature reviews as needed

Key requirements: 2+ years in clinical science or related role in pharma, CRO, or biotech Master/PhD, PharmD, MD, or equivalent health science degree Experience in oncology clinical trials Experience with data analysis and interpretation for safety/pharmacovigilance Strong ability to analyze and interpret complex scientific data to inform strategy Working knowledge of biostatistics, GCP, and regulatory requirements for clinical studies Ability to operate in a fast-paced, team-based matrix environment and independently when needed Strong communication and multitasking skills Excellent interpersonal, verbal, and written communication Collaborative mindset with cross-functional teams Independent decision-making and timely judgment Data analysis and interpretation of clinical trial data Pharmacovigilance principles Biostatistics knowledge