Vice President, Clinical Research-Infectious Disease

What You'll Do

• Serve as a strategic clinical leader, shaping creative and efficient development strategies for multiple pipeline assets
• Lead clinical research sub-teams through direct management of MDs and clinical scientists
• Lead regulatory interactions to advance molecules through development and secure global regulatory approvals
• Collaborate with relevant functions to ensure strategic integration of product development plans
• Oversee all major written deliverables (protocols, clinical sections of regulatory submissions, publications, abstracts) and presentation materials
• Collaborate with Research and Translational Development to identify drug targets and disease indications, and shape clinical development plans
• Be accountable for all relevant timelines and deliverables
• Serve as a key spokesperson at external meetings, including regulatory and scientific forums

Who You Are And What You Bring

• MD, DO, or PharmD with a strong research background; specialty training in Infectious Diseases preferred
• 8+ years of progressive clinical development experience with a strong record of strategic trial design, late-stage execution, and cross-functional leadership
• Proven track record leading registrational trials and marketing applications (NDA/BLA/MAA) through to approval required
• Deep experience in regulatory interactions with global health authorities, including leading filing strategy and submissions
• Current working knowledge of legal, regulatory, and compliance regulations and guidelines; strong understanding of clinical trial design, execution and statistics
• Adaptable and able to effectively lead, collaborate and influence across a complex matrix organization
• Demonstrated leadership in ambiguous situations; able to inspire a team to excel by fostering a climate of energy, excitement and personal accountability