Lead end-to-end project management of **CMC drug development programs**
Develop and maintain **project plans, timelines, and deliverables**
Coordinate cross-functional teams including **Process Development, MSAT, Manufacturing, QA, and Regulatory**
Manage **project risks, budgets, and resources**
Drive execution of programs aligned with **technical and business objectives**
Track and communicate **project status to stakeholders and leadership**
Support **tech transfer, process development, and manufacturing readiness activities**
Ensure alignment with **GMP requirements and internal standards**
Facilitate team meetings and ensure accountability across workstreams

Requirements

5+ years of experience in **biopharma / life sciences project management**
Strong background in **CMC drug development**
Experience working in a **GMP-regulated environment**
Proven ability to manage **cross-functional teams in a matrix organization**
Hands-on experience with **project planning tools (MS Project or similar)**
Strong understanding of **drug development lifecycle (IND to commercialization)**
Experience with **cell therapy or biologics**
Exposure to **tech transfer, MSAT, or manufacturing operations**
PMP certification

Benefits

Competitive hourly rate: $61.10/hr to $74.55/hr. ** (W-2 only, no C2C)**
Hybrid position - 50% onsite required
Working Hours: Monday - Friday, regular business hours
10-month contract with possible extension
Health insurance, holiday pay, 401(k) program, and other benefits

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools

CMC drug developmentproject managementproject planningrisk managementbudget managementprocess developmenttech transfermanufacturing readinessdrug development lifecyclecell therapy

Soft Skills

leadershipcommunicationteam coordinationaccountabilitystakeholder management

Certifications

PMP certification