Medical Director, Early Phase and PK

Responsibilities:

• Bring medical and scientific expertise to the design, execution, and interpretation of FIH, Phase 1, and Phase 2 clinical studies ensuring patient safety and scientific integrity
• Author and oversee key clinical documents — including protocols, amendments, informed consent forms, investigator brochures, clinical study reports, and regulatory submissions (e.g., INDs, CTAs, DSURs).
• Respond to health authority and IRB inquiries for respective studies

Qualifications:

• Advanced degree (M.D., D.O, D.N.P, Ph.D. etc.) required
• 3-5 years of clinical development experience within contract research, pharmaceutical, or academic settings, with a focus on early-stage development or translational research
• Experience designing and running clinical pharmacology studies (preferred), or studies with PK and PD endpoints in healthy volunteers and/or patient populations

Benefits:

• 100% paid health benefits including Medical, Dental and Vision for you and your dependents
• 401(k) program with company match and vesting after the turn of the first month after your start date
• Flexible time off