Director, Program Management, Late-Stage Development
Job in
Gaithersburg, Montgomery County, Maryland, 20883, USA
Listed on 2026-08-30
Listing for:
Scorpion Therapeutics
Full Time
position Listed on 2026-08-30
Job specializations:
-
Business
Regulatory Compliance Specialist, Operations Management
Job Description & How to Apply Below
Key Responsibilities
- Lead and drive cross-functional, late-stage clinical-stage program teams to develop and deliver the Immunocore portfolio; translate program strategies into cross-functional plans and ensure delivery.
- Partner with the Program Lead to drive cross-functional alignment and delivery of assigned programs.
- Provide program management leadership: input into project strategy/vision; ensure alignment with operational delivery.
- Lead development and launch planning (including alternatives and scenario planning); manage marketing authorization submissions and cross-functional launch/new product introduction with Commercial.
- Partner with functional areas (pre-clinical, manufacturing, regulatory, clinical, safety, data management) to refine integrated program strategy/timelines, identify critical path, and keep programs on track.
- Establish short/long-term goals; proactively identify issues/risks and facilitate mitigation.
- Coach teams through issue resolution, decision-making, and contingency planning for complex issues.
- Monitor deliverables; provide regular stakeholder updates via dashboards/reporting/tools.
- Perform day-to-day program management (meetings, agendas/minutes, action items); develop governance and strategic presentations.
- Maintain program management best practices; provide standards/templates guidance; champion program management methodologies.
Supervisory Responsibility: N/A
Education & Qualifications- BS/BA or higher in a life science discipline (or equivalent).
- Typically requires a Bachelor’s degree and 16+ years related experience (or equivalent).
- MS/PhD/PharmD/MBA in immunology, biochemistry, cell biology, or related.
- Prior BLA/MAA filings and new product launch experience.
- PMP certification (preferred).
- 12+ years relevant biotech/pharma experience in R&D project or product management.
- Extensive late-stage R&D drug development knowledge.
- Proficiency with MS Project/Smartsheet and PM tools/processes.
- Strong cross-functional leadership, stakeholder management, communication, and organizational skills.
- Familiarity with Microsoft environment (Word, Excel, PowerPoint, Visio, SharePoint, Teams).
- Delivery-focused, proactive risk/issue identification and solutioning.
- Standard company benefits (medical, dental, vision, time off, 401k) and participation in annual incentive plans.
- $157,500 - $245,000
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