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Cmc Project Coordinator Jobs (NOW HIRING)

Revance

Project Coordinator

Newark, CA

$77K - $97K/yr

The Project Coordinator is a key member of the Project Management Office, supporting high-volume ... Experience supporting GxP, CMC, quality, validation, or regulatory documentation, particularly in ...

Staffingine LLC

CMC Writer

Paramus, NJ · On-site

Support the coordination and preparation of timely CMC file for AR/DSUR/RTQ submissions * Authoring ... Project management skill is plus * Author and review CMC sections of regulatory submissions ...

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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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What cities are hiring for Cmc Project Coordinator jobs? Cities with the most Cmc Project Coordinator job openings:
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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 Program Management - Drug Product

Centessa Pharmaceuticals, LLC

Boston, MA • On-site

$253K - $265K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 21 days ago

Job description

Centessa Pharmaceuticals plc (Nasdaq: CNTA) new kind of pharmaceutical company with a deconstructed R&D environment that prioritizes data driven decision making led by subject matter experts. Centessa is advancing a portfolio of high conviction programs with strong biological validation.
Our asset-centric model offers a unique R&D logic that has been applied by single asset companies to improve productivity. This operating model has minimal centralized infrastructure, reduced hierarchy, and exclusive focus on data driven capital allocation. Our teams are uniquely incentivized to expeditiously interrogate key scientific hypotheses. We believe the asset-centric model can lead to improved success rates for programs with greater speed and modest costs.
Description of Role
Centessa is seeking a Director of CMC Program Management for Drug Product. The CMC PM will provide leadership and operational support to the development and manufacturing of our small molecule programs and actively engage with internal teams and external contract manufacturing organizations. The individual will drive effective execution of CMC deliverables by the project teams in coordination with and support of program and corporate goals. The ideal candidate should be highly organized and an exceptional communicator with experience leading early phase pre-IND teams through late-stage CMC Registration/Commercial validation and launch activities. Travel to vendors both domestically and internationally will be required.
Key Responsibilities
  • Serve as the main point of contact for all CMC project-related communications especially focused on drug product development, manufacturing, release, packaging, labeling, and stability coordination
  • Foster strong relationships with internal teams, and external partners including CDMOs.
  • Participate in regular telecon meetings with CDMOs to maintain the business relationship, progress, meeting notes and action items.
  • Monitor timelines and contracts for accuracy and follow up on any discrepancies with contractors and/or internal personnel.
  • Support CMC activities including tracking relevant GMP and Regulatory documentation.
  • Interfaces with drug substance, drug product, analytical, non-clinical, clinical, Regulatory, supply chain, and Quality colleagues to ensure all projects are delivered on time, within scope and budget.
  • Work with CMC team members to identify resource constraints, risks, and conflicts that could impact the team's bandwidth and/or company timelines.
  • Cover all other project management requirements including shipment/logistics coordination, inventory, and production planning.
  • Drive the development and management of detailed and integrated development plans for CMC projects that account for all phases of drug development across functions with timelines, work plans including interdependencies, gating items, budget, and risk management strategies.
  • Oversee the delivery of project objectives per the program strategy, with a strong focus on meeting critical milestones, and managing scope changes while integrating project constraints.
  • Facilitate effective collaboration across CMC functional teams, ensuring alignment on project goals and priorities.
  • Communicate project updates consistently to various stakeholders, about strategy, adjustments, and development progress.
  • Experience utilizing project management tools and best practices to support CMC activities.
  • Excellent attention to detail, communication, time management, organizational skills, and flexible attitude to work assignments and new learning with proven ability to interact in a team environment.
  • Comfortable in a fast-paced small company environment with the ability to manage a variety of projects simultaneously and handle rapidly changing information.
  • Project management professional (PMP) certification preferred.
  • Expert MS Office skills including Excel, PowerPoint, MS Project, and other PM timeline software (e.g. Smartsheet).

Qualifications
  • BS/MS in a scientific discipline; PhD preferred
  • 10+ years of pharmaceutical industry experience, including 7+ years leading CMC project/program management activities
  • Proven experience in small molecule drug development, with emphasis on drug product development and manufacturing required
  • Strong understanding of the end-to-end drug development process, including CMC, non-clinical, clinical, and regulatory activities
  • Demonstrated knowledge of CMC requirements across all phases of clinical development
  • Thorough understanding of cGMP regulations for pharmaceutical products
  • Experience coordinating and managing CDMO activities supporting development and commercialization
  • Strong project management, organizational, and prioritization skills to manage multiple, evolving programs
  • Excellent decision-making, analytical, and resource management skills in dynamic, global environments
  • Effective communicator with the ability to clearly convey complex scientific information both verbally and in writing
  • Ability to work independently while collaborating cross-functionally and with stakeholders at all organizational levels
  • Self-motivated, results-driven, adaptable to changing priorities, and willing to travel domestically and internationally

Compensation
The annual base salary range for this level is $210,000.00 to $240,000.00. Individual compensation within this range will be determined based on a variety of factors, including qualifications, skills, relevant experience, and job knowledge.
In addition to base pay, this role is eligible for a discretionary annual bonus. Centessa also offers a comprehensive benefits package, which includes a 401(k) plan, company-sponsored medical, dental, vision, and life insurance, generous paid time off, and a health and wellness program.
Work Location
The Director CMC Program Management, Drug Product role is based in the US, with domestic and international travel.
POSITION: Full-Time, Exempt
EEOC Statement: Centessa Pharmaceuticals believes in a diverse environment and is committed to equal employment opportunity for all its employees and qualified applicants. We do not discriminate in recruitment, hiring, training, promotion, or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Centessa Pharmaceuticals will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
Please note: We will not assign referral rights for any unsolicited resumes from recruitment agencies.

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