Oncology Clinical Scientist – Remote-friendly Trials

Arcus Biosciences, Inc.; United States; A distancia; USD 165.000 - 180.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Stock programs

Performance-based bonus

Comprehensive benefits package

Descripción de la vacante

Arcus Biosciences, Inc. is seeking a Clinical Scientist to drive design, planning, and implementation of protocol-specific activities within clinical development programs.

The role involves collaboration on cross-functional study teams to design, execute, and monitor clinical trials, with emphasis on data interpretation and communication to stakeholders. The successful candidate will contribute to regulatory activities and process improvements, supporting internal and external partners.

Formación

• 2+ years as a clinical scientist or related role.
• Experience in oncology clinical trials.
• Knowledge of biostatistics, GCP, and regulatory requirements.

Responsabilidades

• Conduct clinical studies with cross-functional teams under senior oversight.
• Support medical monitoring, safety reviews, and site interactions.
• Analyze clinical trial data for safety and efficacy and provide preliminary assessments.
• Assist in communicating trial results and preparing study documents.
• Coordinate data reviews and updates for data monitoring committees and other data reviews.
• Contribute to authoring study protocols, CSR, IBs, ICFs, and regulatory documents.
• Interact with internal/external stakeholders to support trial objectives.
• Conduct literature reviews as needed.

Conocimientos

Oncology experience

Clinical study design

Data interpretation

Cross-functional teamwork

Regulatory awareness

Educación

Master/PhD in health science or MD/PharmD

Descripción del empleo

Arcus Biosciences, Inc. is seeking a Clinical Scientist to drive design, planning, and implementation of protocol-specific activities within clinical development programs.

The role involves collaboration on cross-functional study teams to design, execute, and monitor clinical trials, with emphasis on data interpretation and communication to stakeholders. The successful candidate will contribute to regulatory activities and process improvements, supporting internal and external partners.