You define clinical trial-related goals and objectives.
You conduct literature and database research on clinical trials as needed
You are responsible for the relevance and accuracy of medical science underpinning of clinical study concepts (CSC) based on thorough scientific review and consultation with internal and external experts
You are responsible for the medical content of clinical study reports, the analysis of clinical data, including safety monitoring, and all activities and procedures that ensure patient safety
You lead and supervise the Global Clinical Study Team to produce high quality program deliverables on schedule
Maintains and develops relationship with key study investigators
Requirements
An MD or MD/PhD with Oncology clinical fellowship training strongly preferred
At least 3-5 years of translational and/or clinical research experience
Benefits
annual bonuses or other incentive plans
equity awards
pension or retirement benefits
401(k) company match
health and wellness programs
fitness centers
insurance benefits (e.g. medical, dental, vision, life and disability)