Clinical Scientist

Job Summary

A company is looking for a Clinical Scientist to support oncology clinical development programs, focusing on prostate cancer.

Key Responsibilities

• Perform ongoing clinical data review and analysis to ensure data integrity and support safety and efficacy assessments
• Support medical monitoring activities in oncology studies, including review of adverse events and long-term outcomes
• Author and contribute to clinical documents such as clinical study reports, investigator brochures, and regulatory submissions

Qualifications & Experience

• Advanced degree in life sciences or related field
• 5+ years of clinical research experience in biotech/pharma, preferably in oncology
• Experience supporting prostate cancer studies or solid tumors is highly desirable
• Demonstrated expertise in clinical data review and medical monitoring for long-term studies
• Strong background in authoring regulatory and clinical documents