Clinical Scientist

Arcus Biosciences•Brisbane, CA

6d•Remote

About The Position

The Clinical Scientist contributes to the scientific, clinical, and operational scope of clinical development programs, with an emphasis on protocol-specific activities. The role helps drive the design, planning, and implementation of study protocols for assigned investigational products and may support related regulatory activities. Working on cross-functional study management teams, the Clinical Scientist supports the design, execution, and monitoring of clinical trials and assists with data interpretation and communication to internal and external stakeholders. The position may also support clinical department process-improvement initiatives. The role can be based at the Hayward or Brisbane, California location (preferred), or remotely. The anticipated salary range for fully qualified candidates is $165,000–$180,000 USD annually. Actual salary may vary based on factors including education, experience, tenure, skills, abilities, internal equity, and market data. Arcus offers participation in stock programs, a performance-based bonus, and a comprehensive benefits package. Arcus Biosciences is an equal opportunity employer and prohibits discrimination and harassment.

Requirements

At least 2 years of experience at a pharmaceutical, CRO, or biotechnology company as a clinical scientist or in a related role.
Master’s or PhD degree in a health science field, PharmD, MD or non-US equivalent, or another relevant advanced degree in a health science field.
Experience in oncology clinical trials.
Experience with data analysis and interpretation, and understanding of safety and pharmacovigilance principles.
Ability to evaluate, interpret, and present complex scientific data (preclinical, clinical, and translational) to inform scientific hypotheses and development strategy.
Working knowledge of biostatistics, GCP, and regulatory requirements for clinical studies.
Ability to work effectively in a fast-paced, team-based matrix environment and independently as appropriate.
Flexibility to accommodate changes in team and project needs.
Ability to handle multiple projects at a time.
Excellent interpersonal, verbal, and written communication skills.
Ability to make independent, timely, and appropriate decisions.
Willingness and ability to think innovatively and tactically, with an interest in clinical research and drug development.

Responsibilities

Partner with cross-functional teams, with oversight from senior team members, to conduct clinical studies, including operational feasibility, data management deliverables, meeting materials, communication plans, safety and medical monitoring, status update reports, and study close-out activities.
Support senior team members with medical monitoring reports, safety reviews, site interactions, and review of tables, figures, and listings (TFLs).
Provide analytical support for clinical trial safety and efficacy data as needed, including gathering, analyzing, reviewing, interpreting, and providing preliminary assessments and recommendations.
Analyze information to assess issues relating to protocol conduct or individual subject safety.
Assist in communicating a clear overview of trial results.
Provide organizational support for Data Monitoring Committees and other applicable data review committees, including operationalizing charters, preparing updates and data reviews, executing meetings and adjudications, and communicating synthesized data reports.
Contribute to authoring study protocols, clinical study reports, investigator brochures (IBs), informed consent forms (ICFs), training documents, and other clinical and regulatory documents.
Interact with internal and external stakeholders, including study sites, vendors, and committees, in support of clinical trial objectives.
Conduct literature reviews as needed.
May support internal process-improvement initiatives within the clinical department.