The Medical Director is primarily responsible for overseeing the direction, planning, execution, and interpretation of clinical trials and the data collection.
In Short
Directs protocol implementation including site identification and communication.
Manages program development across various disciplines.
Interacts closely with the pre-clinical team.
Monitors clinical trials and ensures safety.
Supports data analysis and clinical study report writing.
Collaborates with Medical Affairs and Regulatory groups.
Adheres to company values and ethics.
Performs miscellaneous duties as assigned.
Travel time is approximately 15% to 25%.
Requirements
Board Certified MD with minimum 2 years of industry experience.
Effective oral and written communication skills.
Demonstrated independence and initiative.
Subspecialty training in oncology preferred.
Outstanding academic achievement and clinical trial experience preferred.