precisionmedicinegroup
Vice President, Clinical Development
At a Glance
- Location
- United States
- Work Regime
- remote
- Experience
- 10+ years
- Posted
- 2026-02-17T16:50:33-05:00
Key Requirements
Domain Knowledge
- Clinical
- Education
- Medical
- Regulatory
Benefits & Perks
onary annual bonus, health insurance, retirement savings benefits, life insu
Requirements
Successful completion of MD, MBBS, or equivalent training plus completion of training including a fellowship (Endocrinology, Rheumatology, Hematology-Oncology or other related field, board certification preferred, including European equivalents).
Experience in direct interactions with US and/or EU Regulatory Authorities
At least 10 years of senior leadership experience in the clinical research industry with a demonstrated knowledge and substantial experience including related disciplines (i.e. operations, medical monitoring, biostatistics, regulatory, preclinical, translational pharmacology, etc.) Or equivalent combination of education, professional training and experience that provides the individual with the required knowledge, skills, and abilities to perform the job.
Responsibilities
Precision is seeking an experienced and passionate regulatory physician to join our team as Vice President, Clinical Development. The Vice President, Clinical Development will have a demonstrated background in Autoimmune. The ideal candidate will have a deep understanding of the US Food and Drug Administration framework, and innovative regulatory strategies to accelerate drug development.
The Vice President, Clinical Development will be responsible for driving product development across the Precision portfolio, including drugs, biologics, and cell and gene therapies for autoimmune conditions. The role will focus on regulatory strategy and clinical development, for early to late phase trials.
Reports to Chief Medical Officer, and across Precision for Medicine, supporting medical strategy.
Provides medical and strategic support for business development activities globally including client engagement, proposal support, client capabilities meetings, and professional meetings.
Provides strategic drug development consulting to autoimmune, rare and orphan disease clients. The consulting will be provided in the context of an integrated strategy with medical, clinical, regulatory, biostatistical, translational and marketing insights.