Director/Senior Director, Program Leadership

Role Description

As the Director/Senior Director, Program Leadership, you will own the operations and execution of advancing assets through IND-enabling studies, CMC, and regulatory submission across multiple programs. You will play a central role in moving programs efficiently toward the clinic while helping shape how program leadership operates and scales within the company.

Reporting to the Chief Operating Officer, you will bring deep experience in preclinical program leadership, strong strategic and operational judgment, and clear communication to ensure programs progress effectively across complex, interdependent workstreams.

Location: Remote

What You’ll Do

• Own the full program lifecycle from candidate nomination through IND clearance and Phase 1 enablement across multiple assets in parallel
• Drive the critical path, including timelines, budgets, dependencies, and decision points
• Build and maintain integrated development plans spanning nonclinical, CMC, analytical, formulation, and regulatory workstreams
• Translate program progress into clear, actionable updates and recommendations for leadership
• Own external partnerships with CROs and CDMOs, including vendor selection, scope definition, and ongoing performance management
• Negotiate scope, cost, timelines, and deliverables and hold partners accountable to outcomes
• Coordinate across multiple vendors simultaneously, managing handoffs, data flow, and interdependencies
• Partner with internal technical experts to design studies and translate program needs into effective external workstreams
• Oversee development of study protocols, incorporating cross-functional input and aligning stakeholders
• Build the internal playbooks, processes, and operating structures needed to scale program execution across the pipeline

Qualifications

• Direct operational ownership of multiple IND programs in biologics, with at least one specifically in functional protein therapeutics
• Advanced degree in biochemical, pharmacology, toxicology or related field such as biology and life sciences
• 8+ years (Ph.D.) to 12+ years (Master’s) of relevant industry experience
• Demonstrated success leading programs through CROs and CDMOs, including global vendors
• Deep understanding of the drug development process from discovery through IND filing
• Strong familiarity with GxP, ICH guidelines, and FDA preclinical requirements
• Proven ability to align and influence stakeholders across functions and organizations

Requirements

• Strong strategic and operational judgment
• Clear, concise communicator who can simplify complex programs
• Highly organized and detail-oriented, with the ability to anticipate challenges
• Hands-on leader who is comfortable owning outcomes directly
• Effective at influencing without formal authority
• Comfortable operating in a fast-moving, evolving environment

Benefits

• Opportunity to drive multiple programs from early development through IND and into the clinic in a highly integrated, fast-moving environment
• Ability to work at the intersection of AI, biology, and experimental science on problems where the path forward is not always clear
• Significant ownership and influence on how programs are executed, prioritized, and scaled as the pipeline grows
• Exposure to both strategic decisions and hands-on execution in a lean team where your work directly impacts program outcomes

Additional Information

Compensation Range: $175,000 - $250,000. Individual compensation within this range is determined by a combination of factors, including but not limited to level, years of relevant job-related experience, and internal equity. This is what we believe in good faith is the range of possible base salary for this role at the time of this posting. We may ultimately pay more or less than the posted range. This range may be modified in the future.