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Cmc Project Coordinator Jobs (NOW HIRING)

taiho

Director, Regulatory Affairs CMC

Princeton, NJ · Hybrid

$157K - $207K/yr

... TOI) projects; provides strategic regulatory guidance especially for CMC during drug development, approval and post approval processes and commercialization, in coordination with internal staff ...

Critical Innovations

Director of CMC

Lawndale, CA · Hybrid

... coordination to ensure alignment between other departmental partners. This position does not ... The Director of CMC must be able to work independently, manage multiple projects, and operate ...

Altimmune

CMC Director, Regulatory Affairs

Gaithersburg, MD · On-site

$162K - $213K/yr

Manages global CMC regulatory projects as assigned and assists in the development of relevant ... briefing packages and coordinates meetings with regulatory agencies * Leads CMC-related FDA ...

Altimmune

CMC Director, Regulatory Affairs

Gaithersburg, MD · Remote

$153K - $202K/yr

Manages global CMC regulatory projects as assigned and assists in the development of relevant ... briefing packages and coordinates meetings with regulatory agencies * Leads CMC-related FDA ...

TekWissen LLC

CMC Writer

Paramus, NJ · On-site

$45 - $50/hr

Support the coordination and preparation of timely CMC file for AR/DSUR/RTQ submissions * Authoring ... Project management skill is plus Key Responsibilities * Regulatory Documentation: Author and review ...

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How much do cmc project coordinator jobs pay per hour?

As of Jun 22, 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.
Specialist - Project Management & Strategic Operations (Contract)

Specialist - Project Management & Strategic Operations (Contract)

Vertex Pharmaceuticals Incorporated

Boston, MA • On-site

$35 - $38/hr

Other

Posted 24 days ago

Job description

Job Description
Title/Role: Project Management & Strategic Operations Specialist
Area: Pharmaceutical Sciences
General Position Summary:
The Project Management Specialist performs a variety of well-defined project support assignments for CMC teams, working under a moderate degree of supervision. The incumbent may be responsible for supporting one or more specific Group/Department service functions.
This role is Hybrid. 3 days on site required.
6 month contract, with the chance to extend.
Key Duties and Responsibilities:
  • Performs key administrative functions for the larger CMC Project Management team's contracting and business needs including entering contract requests into Icertis contracts management system and any subsequent purchase order requisitions into the Coupa system.
  • Supports Capital Equipment (CAPEX) operations and business processes including using ServiceNow and Coupa systems for equipment order entry
  • Supports Flexible FTE (FLEX) program operations and business processes including management of Smartsheet tool for legal review and approval of related technical documents and RFPs and submits to selected vendors.
  • Support shipping requests and facilitate shipping transactions in VITAL system
  • Executes purchase orders for suppliers and coordinates material deliveries
  • Works with various cross-functional groups (such as Quality, CMTO, Trade Compliance, Regulatory, suppliers, etc.) to proactively and collaboratively resolve issues that may block the flow of materials or projects
  • Assists with offsite and onsite material inventory storage needs including shipment and pickup of onsite and offsite materials as needed.
  • Performs other duties as assigned

Minimum Qualifications:
  • Associate/Bachelor's degree in relevant discipline
  • Typically requires 2 years of relevant work experience, or the equivalent combination of education and experience
  • Works effectively across departments and levels, building and maintaining productive relationships
  • Ability to effectively balance customer expectations with internal/team expectations.
  • Knowledge of Coupa, Icertis and Oracle - based systems
  • Proficient in Microsoft Office applications
  • Strong prior experience in the pharmaceutical industry

Pay Range
$35-$38/HR
Requisition Disclaimer
This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals ("Vertex"). The individual selected for this role will be offered the role as an employee of a third- party agency partner; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements
By applying for this position, you agree to the Atrium Terms and Conditions and you direct Atrium to share your application materials, which may include your CV/Resume, email address or phone number, with Vertex. For more information on how Vertex handles your personal data related to your job application, please see Vertex's Careers Privacy Notice. Agreeing to the Atrium Terms and Conditions, includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings, profiles, articles, news, and other employment-related information, as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners
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If you do not agree with the Atrium Terms and Conditions, you can still complete your application for this position by emailing your resume to our team at tempstaffing@vrtx.com. Please include the job title in the subject of your email.
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