Clinical Scientist

Worldwide Clinical Trials seeks a Clinical Scientist to review and interpret oncology clinical data from solid tumor studies, communicating findings to clients and study teams. The role involves data analysis, safety monitoring, regulatory support, and cross-functional collaboration within a global CRO environment.

Responsibilities

• Develop oncology clinical data review plans and conduct ongoing analysis of efficacy and safety data
• Present clinical trends and findings to Medical Monitors, Study Teams, and Clients
• Collaborate with cross-functional teams to ensure accurate protocol-defined data collection and reporting
• Track and analyze safety events with Pharmacovigilance and contribute to study modification discussions
• Support regulatory and clinical reporting documents including CSRs, INDs, and NDAs/BLAs

Requirements

• Advanced degree (PharmD, PhD, MSN, ARNP) with 8+ years oncology industry experience
• Deep knowledge of oncology clinical development, study design, and product profiles
• Experience with solid and liquid tumor data review and imaging analysis
• Proficiency with electronic data capture systems and data visualization tools
• Solid understanding of GCP, ICH guidelines, and regulatory requirements
• Excellent written and oral communication and presentation skills
• Strong organizational, analytical, and problem-solving abilities

Compensation: $79,000.00 - $157,000.00 annually