Director Program Management - Biostatistics
Director, Program Management
Overview
We are seeking an experienced Program Management leader to oversee cross-functional development programs within a clinical-stage biotechnology company. This individual will partner closely with Research, Clinical Development, Regulatory, Clinical Operations, Biometrics, CMC, and Finance teams to drive strategic planning, operational execution, and achievement of key program milestones.
The ideal candidate brings a strong background in drug development, exceptional organizational skills, and the ability to lead complex programs in a collaborative, fast-paced environment.
Key Responsibilities
- Partner with cross-functional teams to support program strategy, planning, and execution across development-stage assets.
- Develop and maintain integrated program plans, timelines, budgets, and key milestones.
- Drive alignment across functional leaders to support execution of clinical and regulatory objectives.
- Identify project risks, dependencies, and resource constraints, and proactively develop mitigation strategies.
- Lead cross-functional team meetings, ensuring clear communication of priorities, decisions, action items, and deliverables.
- Track critical path activities and provide timely updates to leadership regarding program progress and challenges.
- Facilitate development and maintenance of integrated project timelines and resource plans.
- Collaborate with internal teams and external partners to coordinate development activities and achieve program goals.
- Partner with Finance and department leaders on forecasting, resource planning, and budget management.
- Support governance processes and provide program-level insights to enable effective decision-making.
Qualifications
- Bachelor's degree in Life Sciences or a related scientific discipline required; advanced degree (MS, PhD, PharmD, or equivalent) preferred.
- 10+ years of experience within the biotechnology or pharmaceutical industry.
- Demonstrated experience leading complex, cross-functional drug development programs.
- Strong understanding of clinical development, regulatory processes, and product development lifecycles.
- Experience managing program timelines, budgets, resources, and stakeholder communications.
Preferred Skills & Experience
- Strong leadership and influence skills with the ability to build alignment across diverse teams.
- Excellent communication, facilitation, and stakeholder management capabilities.
- Proven ability to identify risks and drive solutions in a dynamic development environment.
- Experience supporting programs within immunology, autoimmune disease, inflammation, or related therapeutic areas is highly desirable.
- Highly organized with exceptional attention to detail and follow-through.
- Ability to thrive in a fast-paced, evolving biotechnology setting.
- Proficiency with Microsoft Office Suite and project management tools.
- Demonstrated commitment to collaboration, accountability, integrity, and scientific excellence.
Location
- Remote position
- East Coast candidates strongly preferred
- Ability to travel periodically for team meetings, leadership sessions, and key business activities as needed.
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