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CMC Project Manager

Belgium, WI · On-site

CMC Project Manager ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

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How much do director cmc project management jobs pay per year?

As of Sep 10, 2026, the average yearly pay for director cmc project management in the United States is $124,379.00, according to ZipRecruiter salary data. Most workers in this role earn between $101,000.00 and $147,500.00 per year, depending on experience, location, and employer.

What is a director CMC project management?

A Director of CMC (Chemistry, Manufacturing, and Controls) Project Management oversees the development and execution of strategies related to the manufacturing and regulatory aspects of pharmaceutical products. They coordinate cross-functional teams to ensure that drug development, scale-up, and production processes meet regulatory requirements and project timelines. This role involves managing budgets, timelines, risk assessments, and communication between scientific, manufacturing, and regulatory departments. The Director also plays a key part in preparing documentation for regulatory submissions and ensuring compliance with global health authority standards.

How does a director CMC project management typically collaborate with cross-functional teams to ensure project success?

A Director of CMC Project Management works closely with teams across regulatory affairs, manufacturing, quality assurance, and research and development. They serve as the central point of contact, aligning project timelines, budgets, and deliverables while proactively identifying and mitigating risks. Regular cross-functional meetings, detailed project tracking, and transparent communication are key to ensuring all stakeholders are informed and aligned. This collaborative approach helps streamline processes, address challenges promptly, and keeps projects moving efficiently toward regulatory milestones.

What are the key skills and qualifications needed to thrive as a director CMC project management, and why are they important?

To thrive as a Director CMC Project Management, you need deep expertise in chemistry, manufacturing, and controls (CMC), project leadership experience, and an advanced degree in a scientific discipline. Familiarity with regulatory requirements, quality management systems, and project management tools like MS Project or Smartsheet is typically required. Strong strategic thinking, cross-functional communication, and stakeholder management skills set standout leaders apart in this role. These capabilities are crucial for ensuring compliant, timely, and efficient development and manufacturing of pharmaceutical products.

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What are popular job titles related to Director Cmc Project Management jobs?

For Director Cmc Project Management jobs, the most frequently searched job titles are:

Senior Manager, CMC Project Management

Redwood City, CA • Hybrid

Revolution Medicines
See more jobs at Revolution Medicinesexternal

Full-time

This job post has expired 2 days ago. Applications are no longer accepted.

Job description

The Opportunity:

Revolution Medicines is seeking a motivated individual with a scientific background and project management experience to add to the CMC Project Management team within the PDM function (Pharmaceutical Development and Manufacturing). This position will be responsible for managing cross-fuctional CMC project management activities in support of Revolution Medicines' pipeline compound development and clinical programs. This role is an individual contributor with team leadership responsibilities, reporting into the Associate Director, CMC Project Management.

Responsibilities:

  • Provide project management support to CMC teams for projects ranging from Pre-IND through different phases of clinical development and commercialization.

  • Track CMC timelines, deliverables and other relevant documents.

  • Collaborate with team members in PDM, QA, clinical and non-clinical development teams to ensure project activities are progressing within established timelines

  • Coordinate with the Regulatory Affairs team to track, coordinate, and communicate CMC regulatory filing timelines as needed.

  • Collaborate with CMC leads to plan and facilitate regular and effective CMC project meetings with structured agendas and accurate meeting minutes; follow up on action items.

  • Proactively identify potential key issues and communicate with key stakeholders and management in a timely manner.

  • Provide project management support to enable oversight of the development activities outsourced to CDMO(s) as needed.

Required Skills, Experience and Education:

  • B.S with 10+ years/M.S with 5-8 years/Ph.D with 3-5 years experience in Pharma/Biotech industry.

  • Strong CMC project management experience for development projects spanning various phases of development with a good understanding of the drug development cycle, regulatory filings experience a plus.

  • Knowledge of current International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) guidelines, GMP guidelines, and related industry practices.

  • Working experience and knowledge of regulatory submission (Investigational New Drug (IND), Investigational Medicinal Product Dossier (IMPD), and / or New Drug Application (NDA).

  • Demonstrated experience working in cross-fuctional teams and effective communication across multiple functional areas.

  • Effective written and verbal communication skills and interpersonal skills.

  • Ability to interpret complex project information and identification of potential timeline and project risks.

Preferred Skills:

  • Small molecule development experience.

  • B.S. or M.S. or Ph.D. degree in Pharmaceutics, Chemistry, Chemiscal engineering or closely related field is desirable.

#LI-CT1 #LI-Hybrid

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