Oncology Clinical Scientist – Remote

Arcus Biosciences, Inc.; Brisbane (CA); Presencial; USD 165 000 - 180 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Stock options

Performance-based bonus

Comprehensive benefits package

Resumo da oferta

Arcus Biosciences, Inc. is seeking a Clinical Scientist to contribute to design, planning, and execution of oncology-focused clinical development programs.

The role involves cross-functional collaboration across study teams, data interpretation, and supporting regulatory activities. The successful candidate will have 2+ years in clinical science, advanced health science degrees, and experience with safety monitoring and biostatistics, enabling effective communication of complex trial results to

Qualificações

• 2+ years as a clinical scientist or related role in pharma/CRO/biotech
• Master/PhD or PharmD/MD required
• Experience in oncology clinical trials required
• Experience with data analysis and interpretation for safety/pharmacovigilance
• Strong written/verbal communication and cross-functional collaboration
• Knowledge of biostatistics, GCP, and regulatory requirements

Responsabilidades

• Design, plan, and implement study protocols for investigational products
• Support medical monitoring, safety reviews, and-site interactions
• Analyze clinical trial data and provide preliminary assessments
• Communicate trial results clearly to stakeholders
• Assist in protocol, CSR, IBs, ICFs, and other regulatory documents
• Interact with sites, vendors, and committees to support trial objectives
• Conduct literature reviews as needed

Conhecimentos

Clinical development

Data analysis

Biostatistics

GCP/regulatory knowledge

Team collaboration

Problem solving

Formação académica

Master/PhD in health sciences

PharmD/MD or non-US equivalent

Descrição da oferta de emprego

Arcus Biosciences, Inc. is seeking a Clinical Scientist to contribute to design, planning, and execution of oncology-focused clinical development programs.

The role involves cross-functional collaboration across study teams, data interpretation, and supporting regulatory activities. The successful candidate will have 2+ years in clinical science, advanced health science degrees, and experience with safety monitoring and biostatistics, enabling effective communication of complex trial results to