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How much do cmc project coordinator jobs pay per hour?

As of Jun 21, 2026, the average hourly pay for cmc project coordinator in the United States is $28.81, according to ZipRecruiter salary data. Most workers in this role earn between $22.36 and $33.17 per hour, depending on experience, location, and employer.

What is CMC in project management?

In project management, CMC stands for Chemistry, Manufacturing, and Controls, which refers to the processes and documentation required to ensure the quality and consistency of pharmaceutical products. For a CMC Project Coordinator, understanding regulatory requirements and coordinating between R&D, manufacturing, and quality teams is essential to meet project timelines and compliance standards.

Can I make 100k as a project manager?

Cmc Project Coordinators typically earn lower salaries than project managers, with project managers in many industries earning $80,000 to over $120,000 annually depending on experience, industry, and location. Achieving a $100,000 salary often requires several years of experience, relevant certifications like PMP, and strong project management skills. Salary potential increases with responsibility, certifications, and proven success in managing complex projects.

What are the daily responsibilities of a CMC Project Coordinator in the pharmaceutical industry?

As a CMC Project Coordinator, your daily responsibilities typically include coordinating timelines and deliverables for drug development projects, managing documentation for regulatory submissions, and facilitating communication between chemistry, manufacturing, quality, and regulatory teams. You may regularly organize team meetings, track project progress, and identify or resolve bottlenecks. The role often requires balancing multiple projects and ensuring that all tasks adhere to industry quality standards and regulatory requirements. This position is highly collaborative, making it ideal for individuals who enjoy working at the intersection of science, operations, and compliance.

What are the key skills and qualifications needed to thrive in the Cmc Project Coordinator position, and why are they important?

To thrive as a CMC (Chemistry, Manufacturing, and Controls) Project Coordinator, you need a background in pharmaceutical or biotechnology project management, familiarity with regulatory compliance, and a degree in a scientific field. Experience with project management software (like MS Project or Smartsheet), document control systems, and knowledge of regulatory standards such as FDA or EMA guidelines are often required. Exceptional organizational skills, attention to detail, and effective cross-functional communication set top candidates apart. These abilities ensure seamless project execution, regulatory compliance, and successful collaboration across technical and regulatory teams.

What is a CMC Project Coordinator job?

A CMC (Chemistry, Manufacturing, and Controls) Project Coordinator is responsible for supporting project management activities related to pharmaceutical product development and manufacturing. They assist in coordinating timelines, documentation, regulatory submissions, and cross-functional team communications to ensure compliance with industry standards and regulations. Their role helps streamline processes across departments such as R&D, quality assurance, regulatory affairs, and manufacturing. Strong organizational skills and attention to detail are essential for success in this role.

Which is higher a project manager or a project coordinator?

A project manager typically holds a higher position than a project coordinator. The project manager oversees the entire project, makes strategic decisions, and manages the team, while the project coordinator supports the project by handling administrative tasks and coordinating activities. In many organizations, project managers have more authority, responsibility, and often a higher salary than project coordinators.

Is a project coordinator an entry level position?

A CMC Project Coordinator role is often considered entry-level or early-career, requiring basic project management skills, organization, and communication abilities. However, some positions may prefer previous experience or relevant certifications such as PMP or CAPM. The level can vary depending on the company's requirements and project complexity.
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Cmc Project Coordinator jobs near you
Infographic showing various Cmc Project Coordinator job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $59,915 per year, or $28.8 per hour.
Director, CMC Project Management

Director, CMC Project Management

Sionna Therapeutics Inc

Waltham, MA • On-site

$210K - $230K/yr

Full-time

Posted 22 days ago

Job description

Description:

Sionna Therapeutics is a clinical-stage biopharmaceutical company on a mission to revolutionize the current treatment paradigm for CF by developing novel medicines that normalize the function of the CFTR protein. Sionna’s goal is to deliver differentiated medicines for people living with CF that can restore their CFTR function to as close to normal as possible by directly stabilizing CFTR’s nucleotide-binding domain 1 (NBD1), which the company believes is central to potentially unlocking meaningful improvements in clinical outcomes and quality of life for people with CF. Leveraging over a decade of the co-founders’ extensive research on NBD1, the company is advancing a pipeline of novel small molecules engineered to correct the defects caused by the F508del genetic mutation, which resides in NBD1. Sionna is also developing a portfolio of complementary CFTR modulators that are designed to work synergistically with its NBD1 stabilizers to improve CFTR function.

Position Summary:

Sionna Therapeutics is seeking a Director, CMC Project Management who will be responsible for facilitating and coordinating the strategic planning, integration, and execution of the company’s CMC development programs across the portfolio. This position serves as a vital role within CMC, driving cross-functional alignment, integrated planning, and execution from pre-clinical development through commercial readiness.


Reporting to the Senior Vice President of CMC, this individual will partner closely with CMC, Clinical Drug Supply, Regulatory, Quality Assurance, Finance, and Program Leadership to ensure CMC programs are aligned with corporate goals and clinical development plans.


Responsibilities:

Program Management

  • Drive the creation and ongoing management of integrated program plans, including timelines, priorities, milestones, risk registers, and action plans.
  • Manage a portfolio of CMC projects, ensuring alignment with corporate goals and clinical development plans.
  • Support the development of clear, data-driven scenarios and strategic options that enable agility and well-informed decision-making.
  • Facilitate effective cross-functional team coordination, meeting management, and execution against deliverables.
  • Ensure consistent application of project management best practices, including project plans, dashboards, timelines, risk registers, and governance.
  • Identify, establish, and continuously improve project management processes, tools, metrics, and operating models across CMC teams to improve efficiency.

Operational Excellence

  • Ensure CMC project meetings and CMC governance meetings are agenda-driven and focused on efficient decision-making.
  • Coordinate and document agenda and meeting notes for meetings with internal and external stakeholders to ensure clear communication and expectations as well as efficient execution of CMC activities and CMC governance meetings.

Financial Management

  • Manage the CMC project budgets to ensure accurate forecasting, alignment with strategic priorities and accountability across CMC.
  • Facilitate the review and approval of CDMO scopes of work, purchase orders, and invoices.
Requirements:
  • Bachelor’s degree (advanced degree preferred) in Chemistry, Pharmaceutics, or related field.
  • 12+ years of experience in pharmaceutical or biotech industry, with at least 3 years of experience in CMC project management or related technical operations role or equivalent experience.
  • Experience with small molecule and solid oral dosage form development preferred.
  • PMP or PMI certification is beneficial but not required.
  • Experience collaborating with CDMO partners.
  • Demonstrated analytical, problem-solving, and scenario planning skills.
  • Exceptional organizational and communication skills and a demonstrated ability to work independently and collaboratively across all levels of the organization.
  • Curious, adaptable, and energizing leader adept at leading through change.
  • Champions and models the organization’s values, fostering a culture of quality, inclusion, and continuous improvement across all teams.
  • Proficiency with project management tools such as Smartsheet or OnePager preferred.
  • Ability to thrive in a fast-paced, dynamic environment with shifting priorities.

Salary Range: $210,000 – $230,000

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