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Drug Development Project Manager Jobs in Renton, WA

Role IT Project Manager

Seattle, WA

$112.10K - $132.60K/yr

Role: IT Project Manager Location: Seattle,WA Exp: 8+ years Duration: 9 months Mandatory Skills ... Net and Web application development projects Skills Desirable: --Skilled in the use of Unified ...

Project Manager - Land Development Full-time Exempt Professional Kirkland, WA. PACE Engineers, A Verdantas Company , is a Pacific Northwest engineering firm providing civil and structural engineering ...

Project Manager - Land Development Full-time Exempt Professional Kirkland, WA. PACE Engineers, A Verdantas Company , is a Pacific Northwest engineering firm providing civil and structural engineering ...

Project Manager-ADC

Seattle, WA · On-site

$96.15 - $105.77/hr

Comprehensive understanding of drug development process, with working experience across product ... Proficiency with project management tools (e.g., MS Project, Smartsheet) and budgeting/resource ...

Comprehensive understanding of drug development process, with working experience across product ... Proficiency with project management tools (e.g., MS Project, Smartsheet) and budgeting/resource ...

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Showing results 1-20

Drug Development Project Manager information

See Renton, WA salary details

$48.4K

$106.3K

$159.7K

How much do drug development project manager jobs pay per year?

As of May 31, 2026, the average yearly pay for drug development project manager in Renton, WA is $106,342.00, according to ZipRecruiter salary data. Most workers in this role earn between $86,000.00 and $122,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Drug Development Project Manager, and why are they important?

A Drug Development Project Manager requires expertise in pharmaceutical sciences, regulatory requirements, and project management, often supported by a relevant degree and PMP certification. Familiarity with project management tools (like MS Project or Smartsheet), clinical trial management systems, and documentation platforms is essential. Excellent leadership, strategic communication, and problem-solving abilities help navigate complex timelines and cross-functional teams. These skills ensure efficient project execution, regulatory compliance, and successful advancement of drug candidates through development phases.

What are some common challenges faced by Drug Development Project Managers, and how can these be managed effectively?

Drug Development Project Managers often encounter challenges such as coordinating cross-functional teams, managing shifting regulatory requirements, and ensuring projects stay on schedule and within budget. Effective communication and proactive risk management are essential to navigate these complexities. Building strong relationships with stakeholders and maintaining transparent project plans can help address issues early and keep development efforts aligned with company goals.

What does a Drug Development Project Manager do?

A Drug Development Project Manager oversees and coordinates all aspects of pharmaceutical product development, from early research through clinical trials to regulatory approval and market launch. They manage cross-functional teams, timelines, budgets, and communications to ensure projects meet scientific, regulatory, and business goals. These professionals play a critical role in identifying risks, troubleshooting issues, and ensuring compliance with industry standards. Their work helps bring new therapies to market efficiently and safely.

What is the difference between Drug Development Project Manager vs Clinical Research Associate?

AspectDrug Development Project ManagerClinical Research Associate
CredentialsBachelor's/Master's in life sciences, PMP certification often preferredBachelor's in life sciences, clinical research certification beneficial
Work EnvironmentCoordinates multiple teams across drug development phasesMonitors clinical trial sites and ensures protocol compliance
Industry UsageUsed in pharmaceutical and biotech companies during drug developmentPrimarily in clinical trial sites and CROs

The Drug Development Project Manager oversees the entire drug development process, coordinating teams and managing timelines. In contrast, the Clinical Research Associate focuses on monitoring clinical trials at sites to ensure compliance and data integrity. Both roles are essential in the drug development pipeline but differ in scope and responsibilities.

What are popular job titles related to Drug Development Project Manager jobs in Renton, WA? For Drug Development Project Manager jobs in Renton, WA, the most frequently searched job titles are:
What job categories do people searching Drug Development Project Manager jobs in Renton, WA look for? The top searched job categories for Drug Development Project Manager jobs in Renton, WA are:

Senior CMC Project Manager - Cell Therapy / Biopharma

SOKOL GxP Services

Seattle, WA • On-site

$61.10 - $74.55/hr

Contractor

Medical, Retirement

Posted 22 days ago


Job description

SOKOL GxP Services is looking for a Senior CMC Project Manager to lead technical drug development programs within a GMP-regulated environment.

This role will focus on the planning, execution, and delivery of CMC initiatives supporting cell therapy or biologics programs across development and manufacturing.

The Senior Project Manager will operate within a cross-functional environment, driving alignment across Process Development, Manufacturing, MSAT, Quality, and Regulatory teams. This role requires strong ownership of timelines, risks, and deliverables, ensuring programs are executed efficiently and in alignment with overall development strategy.

This is a highly visible role supporting complex, technical programs, requiring both project management expertise and a solid understanding of CMC drug development.

Key Responsibilities
  • 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

Required Experience
  • 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