Provides scientific leadership, direction, and contribution to ViiV Healthcare early clinical development programs.
Contributes to the study team in the design and development of high quality, timely studies.
Liaises with Clinical Pharmacology, Medical, Commercial, and Asset Leads to help ensure study evaluates key aspects of the Asset Product Profile.
Partners with operations colleagues to ensure accuracy, quality, and timeliness of study results.
Requirements
B.S., Masters, Ph.D., Pharm.D., or MD with 3 plus years of recent clinical drug development experience contributing to the scientific aspects of clinical program(s) and regulatory submission(s).
3 plus years contributing to a team, 3rd parties, academic partners, and subcontracted organizations.
Experience with managing multiple programs concurrently