Vice President of Clinical Development
VP__4248771054
Posted: 13/06/2025
- New Jersey, United States (Hybrid)
- Contract
Vice President of Clinical Development
Disease Area: Immunology & Neurology
Location: New Jersey, United States
An innovation-driven biopharmaceutical company is seeking a Vice President of Clinical Development to lead US clinical development strategy with a strong focus on autoimmune diseases and multiple sclerosis. Backed by global R&D and commercial infrastructure, this is a rare opportunity to shape the clinical trajectory of high-potential, first-in-class therapies.
Whats on offer:
Global clinical leadership team with direct influence on pipeline success and scientific strategy.
$320,000-420,000 + bonus and benefits package
About the Role
Responsible for leading clinical development programs from early stages through registration, ensuring scientific excellence, regulatory alignment, and cross-functional coordination. This role demands strategic foresight, strong clinical acumen in neurology/immunology, and the ability to operate in an entrepreneurial, fast-paced environment.
Key Responsibilities
- Lead clinical development strategy for multiple programs across Phases I–III, with particular emphasis on autoimmune and neurology indications.
- Ensure compliance with FDA, ICH, and internal regulatory standards.
- Develop differentiated clinical strategies informed by patient needs and competitive insight.
- Partner closely with research and commercial teams to maximize asset value across the lifecycle.
- Cultivate relationships with KOLs, physicians, and clinical partners.
- Oversee medical governance, safety, and protocol design.
- Build and manage a high-performing medical/clinical development team.
- Contribute to investor engagement and scientific communication at a leadership level.
Candidate Profile
- MD is required or MD/PhD with a strong scientific background in immunology, neurology, or related fields.
- 15+ years of experience in new drug development, including late-stage trials and regulatory submissions.
- Direct experience in autoimmune or MS clinical trials is strongly preferred.
- Strong grasp of US regulatory environment and FDA approval pathways.
- Effective communicator with both internal stakeholders and external clinical/scientific communities.
- Entrepreneurial mindset, execution-focused, and comfortable operating in a lean, cross-functional setting.
Confidential applications welcome. Please share with Nicole Buckland, Executive Consultant
nbuckland@i-pharmconsulting.com or apply via the advert.
Nicole Buckland
Executive Consultant
