Senior Program Manager — Late-Stage Biopharma to Launch

Stevenson Search Partners

Maryland

On-site

USD 130,000 - 190,000

Full time

14 days+
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Job summary

Stevenson Search Partners is seeking a Senior Program Manager/Associate Director, Program Management for a client developing mRNA CAR-T therapies for autoimmune diseases. The role oversees enterprise-level programs, risk management, and readiness for regulatory submission and commercial launch in a regulated environment.

The position involves leading cross-functional initiatives to transition Phase III development toward regulatory submission and successful market introduction, with emphasis on

Qualifications

  • 6+ years of experience in biotech, pharmaceutical, or life sciences
  • Proven experience managing late-stage clinical or pre-commercial programs
  • Experience coordinating cross-functional teams across clinical, regulatory, manufacturing, quality, supply chain, and commercial

Responsibilities

  • Lead integrated program plans across late-stage clinical development, regulatory submission, and pre-commercial activities
  • Coordinate cross-functional teams to ensure alignment on program objectives and execution
  • Develop and maintain program timelines, milestones, and critical path analyses
  • Identify program risks and mitigation strategies with contingency planning
  • Track issues and provide status updates to senior leadership with recommended solutions
  • Develop executive dashboards and communicate program status, timelines, and metrics
  • Collaborate with Commercial teams on launch planning and go-to-market readiness

Skills

Program management
Cross-functional leadership
Regulatory submission

Education

Bachelor's degree in life sciences, business, or related field

Job description

Stevenson Search Partners is seeking a Senior Program Manager/Associate Director, Program Management for a client developing mRNA CAR-T therapies for autoimmune diseases. The role oversees enterprise-level programs, risk management, and readiness for regulatory submission and commercial launch in a regulated environment.

The position involves leading cross-functional initiatives to transition Phase III development toward regulatory submission and successful market introduction, with emphasis on

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