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Cmc Project Coordinator Jobs (NOW HIRING)

A brief overview The CMC Project Leader is responsible for coordinating and proactively managing ongoing active pharmaceutical ingredient (API) manufacturing campaigns for Bachem's biotechnology and ...

A brief overview The CMC Project Leader is responsible for coordinating and proactively managing ongoing active pharmaceutical ingredient (API) manufacturing campaigns for Bachem's biotechnology and ...

A brief overview The CMC Project Leader is responsible for coordinating and proactively managing ongoing active pharmaceutical ingredient (API) manufacturing campaigns for Bachem's biotechnology and ...

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Cmc Project Coordinator information

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How much do cmc project coordinator jobs pay per hour?

As of Aug 3, 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. A CMC Project Coordinator oversees activities related to these areas, coordinating between teams to meet regulatory standards and project timelines. Strong knowledge of regulatory requirements and project management tools is essential for this role.

Is a project coordinator a high paying job?

The salary of a project coordinator varies depending on industry, experience, and location, but it is generally considered an entry- to mid-level position with moderate pay. In some fields like construction or IT, project coordinators can earn higher salaries, especially with certifications or specialized skills. Overall, it is not typically classified as a high-paying role compared to managerial or executive positions.

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.

How much does AstraZeneca pay CMC project managers?

Salaries for CMC Project Managers at AstraZeneca typically range from $90,000 to $130,000 annually, depending on experience, location, and level of responsibility. Compensation may also include bonuses and benefits aligned with industry standards for pharmaceutical project management roles.

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.

What are typical CMC job responsibilities?

A CMC Project Coordinator is responsible for managing and coordinating activities related to Chemistry, Manufacturing, and Controls (CMC) in pharmaceutical development. This includes overseeing documentation, tracking project timelines, ensuring compliance with regulatory standards, and collaborating with cross-functional teams to meet project milestones. Strong organizational skills and knowledge of regulatory requirements are essential for success in this role.
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Infographic showing various Cmc Project Coordinator job openings in the United States as of July 2026, with employment types broken down into 3% Internship, 80% Full Time, 13% Part Time, 2% Contract, 1% Nights, and 1% Summer. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $59,915 per year, or $28.8 per hour.

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Job description

Company Description

A Few Words About Us
Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

Position Details: 

Client Direct Client

Location Lexington, MA

Job Title CMC Project Manager I

Duration 10 Months+

Must have skill-set [Job Description] Requirements

Working with transition team lead apply standardized project tools to manage and document CMC Regulatory Submission transition project progress towards end goals.  

Facilitate project goals and objectives definition with the team and sponsors.  

Update progress against set milestones.  

Keep current development strategies, integrated plans, communication and risk management plans.  

Document scenario planning to support timely decision making to ensure execution per plans. Ensure effective communication and coordination of deliverables.

Work with management or team leader to set agendas, plan activities and facilitate decision making.  

Coordinates team logistics including meeting schedules, meeting materials (agendas, pre-read materials, minutes) and ensures adherence to team goals/objectives.  

Facilitates timely and productive team discussions.

Essential Responsibilities

Support the planning phase and map the transition of CMC Regulatory submission team capturing deliverables, milestones, risks and mitigation plans, priorities, timings, communication strategies, training requirements, resourcing and budgetary requirements.

Engage with key stakeholders for input and endorsement as necessary and communicate on progress 


Experience Requirements

Pharmaceutical industry and specifically within a CMC/Project Management environment

Change management experience

Familiarity with global CMC submission filings





Feel free to forward my email to your friends/colleagues who might be available




Qualifications

Key Skills and Competencies


Strong work ethic and attention to detail


Ability to work independently and as an integral part of a team, take initiative, and complete tasks to deadlines


Ability to manage multiple activities, prioritize effectively, and work to aggressive timelines


Ability to collaborate cross functionally and strong communicator both within line functions and across matrixed teams

Additional Information

Thanks!!!


Warm Regards,


Amrit Singh


Clinical Recruiter


Integrated Resources, Inc


IT REHAB CLINICAL NURSING


Tel: (732) 429 1634  


Fax: (732) 549 5549


http://www.irionline.com


Inc. 5000 - 2007, 2008, 2009, 2010, 2011, 2012,2013 & 2014 (8th Year)


Certified MBE I GSA - Schedule 66 I GSA - Schedule 621I I GSA - Schedule 70



Integrated Resources logo

About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996