Medical expert evaluating safety and managing risk for projects in clinical development and post - marketing. Collaborating with scientists and clinical teams to support safety assessments and regulatory documentation.
About the role
- Senior Clinical Director responsible for planning and directing clinical research activities. Overseeing clinical development for new and marketed oncology medicines across various phases.
Responsibilities
- Planning and directing clinical research activities involving new or marketed medicines
- Evaluating pre-clinical and translational work for early clinical development plans
- Developing clinical development strategies for investigational or marketed drugs
- Medical oversight and overall conduct of clinical trials
- Analyzing and summarizing clinical findings from studies
- Participating in internal and external research project teams
- Actively engaging with functional areas in support of study execution
- Maintaining scientific knowledge and establishing communications with investigators
- Authoring development documents and facilitating collaborations with external researchers
Requirements
- M.D or M.D./Ph.D.
- Minimum of 3 years clinical medicine experience
- Minimum of 3 years of industry experience in drug development or biomedical research
- Demonstrated success in overseeing clinical studies and protocols
- Proven track record in clinical medicine and background in biomedical research
- Strong interpersonal skills, as well as the ability to function in a team environment
- Board Certified or Eligible in Oncology or related discipline (preferred)
- Experience in GU malignancies (preferred)
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
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