VP, Clinical Development & Medical Affairs

Role: Executive Director of Clinical Development & Medical Affairs at Humacyte, leading global clinical trial strategies and corporate medical affairs for bioengineered tissue products. Responsibilities: develop and execute clinical development plans, oversee post-approval studies for trauma and lifecycle indications such as CABG and PAD, provide scientific and regulatory review, lead medical affairs strategies, collaborate with external thought leaders, and represent the company at key industry events. Requirements: MD with 7-10 years pharma/biotech experience, especially in vascular or regenerative medicine; 5-7 years of leadership; experience with NDA/BLA submissions, regulatory compliance, and clinical trial design. High-Value: focus on vascular trauma, CABG, PAD, late-stage clinical trials, regulatory interactions, and medical affairs within bioengineered tissues and regenerative medicine. Work setup: partially remote in Durham, NC; no travel specified.