Responsibilities:
- Responsible for developing and implementing clinical program strategies for phase I-IV studies.
- Participates in preparing regulatory filings (i.e. annual updates, NDAs, INDs, etc.)
- Manages preparation of scientific presentations and publications.
Position Requirements:
- M.D. or PhD required
- Excellent written and oral communication skills
- Scientific publication record
Must be able to perform the essential functions of the position, with or without reasonable accommodation; however, reasonable accommodations will be provided for qualified individuals with disabilities unless doing so would impose undue hardship.
The total compensation package for this position will also include incentive compensation and benefits such as health insurance, unlimited paid time off, parental leave, a 401k matching program, and other benefits to its employees.
If you reside in a state or locality with enacted pay transparency laws, you are entitled to request and receive additional details regarding compensation and benefits. For assistance, please contact us at [redacted] between 8:00 AM and 5:30 PM ET, Monday through Friday.
