Key skills
LeadershipCollaboration
About this role
Role Overview
- Manage studies to provide safety and efficacy data for regulatory approval
- Plan and direct clinical research activities involving new or marketed drugs in Thoracic Oncology
- Oversee entire clinical development cycle including development strategy, study design, and execution
- Analyze and summarize clinical findings from studies to support regulatory reporting and publications
- Manage Clinical Teams in execution of clinical studies
- Interact with internal and external stakeholders for scientific leadership and collaboration
Requirements
- M.D or M.D./Ph.D.
- Must have experience in industry in the field of Thoracic Oncology
- Minimum of 3 years of clinical medicine experience
- Minimum of 5 years of industry experience in drug development
- Demonstrated record of scientific scholarship and achievement
- A proven track record in clinical medicine and background in biomedical research is essential
- Strong interpersonal skills, as well as the ability to function in a team environment, are essential.
Benefits
- medical, dental, vision healthcare and other insurance benefits (for employee and family)
- retirement benefits, including 401(k)
- paid holidays
- vacation
- compassionate and sick days