Program Manager

Contract Program Manager (6 months)

We are seeking a Program Manager (Senior Manager / Associate Director) to lead a cross-functional research team as it progresses through DC and into development. The candidate will drive the successful execution of one of our advanced research programs from early-stage research through the initial regulatory filing and into the clinic. This role is critical in ensuring that project goals are achieved on time, within scope, and budget, while maintaining compliance with regulatory standards and fostering collaboration across internal and external stakeholders. The qualified individual will report to the Program and Portfolio Management and will be a partner in building out various initiatives and processes that will be established as the broader organization grows.

Key Responsibilities

• Support the Asset Team, lead and manage end-to-end the asset lifecycle.
• Develop and maintain detailed project plans, timelines, budgets, and resource forecasts.
• Coordinate cross-functional teams within R&D, including non-clinical, clinical operations, regulatory affairs, manufacturing, and quality assurance.
• Monitor project progress, identify risks, and implement mitigation strategies.
• Ability to serve as the primary point of contact for internal stakeholders and external partners including CROs and other vendors
• Prepare and present project updates, and dashboards.
• Lead project team meetings, drive decision-making, and foster a collaborative environment.
• Manage project budgets and support financial forecasting and reporting.
• Other duties assigned, including assistance of program management & leadership and other organizational support activities.

Qualifications

Required:

• Bachelor's degree in Life Sciences, Biotechnology, Pharmaceutical Sciences, or related field.
• 5+ years of project management experience in the biotech, pharmaceutical, or life sciences industry.
• Proven track record in leading complex, multi-disciplinary projects through various stages of development, to include regulatory filings.
• Knowledge drug development processes and regulatory pathways.
• Strong communication, leadership, and organizational skills.
• Proficiency with project management tools (e.g., Smartsheet, ThinkCell, etc).

Preferred:

• Advanced degree (MS, MBA, or PhD) in a scientific discipline.
• Research Program Management experience.
• Late-stage development experience.
• PMP or equivalent project management certification.
• Experience working in a fast-paced, startup biotech environment.