Key skills
LeadershipCommunication
About this role
Role Overview
- responsible for the planning and directing of clinical research activities involving new or marketed medicines in the Oncology therapeutic area, Hematology section
- manage and oversee the entire cycle of late-stage clinical development from Phase 2 to Phase 5
- lead cross-functional product development teams that oversee program strategy and execution
- provide internal scientific leadership for cross-functional areas supporting clinical trials
- interact externally with key scientific leaders
- evaluate pre-clinical and translational work for the purpose of generating early clinical development plans and Investigational New Drug (IND) applications
- develop clinical development strategies for investigational or marketed medicines
- monitor and manage the conduct of ongoing or new clinical trials for investigational or marketed medicines
- act as an integration of cross-functional input and expertise
- analyze and summarize the clinical findings from studies to support decisions regarding safety and efficacy
Requirements
- M.D or M.D./Ph.D.
- Minimum of 3 years of clinical medicine experience
- Minimum of 5 years of industry experience in drug development with demonstrated success in overseeing multiple studies and protocols through completion
- Experience in authoring regulatory documents and leading discussions with regulatory agencies
- Demonstrated record of scientific scholarship and achievement
- Proven track record in clinical medicine and background in biomedical research
- Outstanding interpersonal and collaborative skills, as well as the ability to function in a matrix environment
- Excellence in delivering clear, impactful communication verbally, in writing, and during presentations
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
- annual bonus and long-term incentive, if applicable