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Cmc Project Manager Jobs in Detroit, MI (NOW HIRING)

MMS

Senior Nonclinical Writer (US)

Canton, MI · On-site

Collaborate with cross-functional teams such as project management, safety, efficacy, biostats, regulatory operations, and CMC. * Demonstrated ability to lead others to complete complex projects.

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Cmc Project Manager information

See Detroit, MI salary details

$44.5K

$104K

$167.8K

How much do cmc project manager jobs pay per year?

As of Aug 31, 2026, the average yearly pay for cmc project manager in Detroit, MI is $103,972.00, according to ZipRecruiter salary data. Most workers in this role earn between $82,200.00 and $127,200.00 per year, depending on experience, location, and employer.

What is a CMC Project Manager?

A CMC (Chemistry, Manufacturing, and Controls) Project Manager oversees the development, manufacturing, and regulatory aspects of pharmaceutical products. They coordinate cross-functional teams, manage timelines, and ensure compliance with regulatory requirements. Their role is critical in guiding drug development from early stages to commercialization while maintaining quality and efficiency.

What are the typical responsibilities of a CMC Project Manager in a pharmaceutical company?

A CMC Project Manager is responsible for coordinating cross-functional teams to ensure successful delivery of project milestones related to product development, manufacturing, and regulatory submissions. Their daily tasks often include developing project timelines, managing risk assessments, overseeing documentation, and facilitating communication between technical, regulatory, and quality departments. They play a pivotal role in preparing CMC sections for regulatory filings, supporting process optimization, and troubleshooting manufacturing challenges. This position requires excellent multitasking abilities and close collaboration with internal stakeholders and external partners throughout the product lifecycle.

What are the key skills and qualifications needed to thrive as a CMC Project Manager, and why are they important?

A CMC Project Manager needs strong expertise in Chemistry, Manufacturing, and Controls (CMC) processes, project management certifications (such as PMP), and a background in pharmaceutical or biotech industries. Familiarity with regulatory submission systems, quality management software, and documentation tools is highly valued. Exceptional organizational skills, problem-solving ability, and effective cross-functional communication help candidates excel in this role. These capabilities are critical for ensuring project milestones are met, regulatory requirements are satisfied, and product development remains on track.

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Cities near Detroit, MI with the most Cmc Project Manager job openings:

    Cmc Project Manager jobs near you
    Infographic showing various Cmc Project Manager job openings in Detroit, MI as of August 2026, with employment types broken down into 86% Full Time, 12% Part Time, and 2% Contract. Highlights an 84% Physical, 2% Hybrid, and 14% Remote job distribution, with an average salary of $96,098 per year, or $46.2 per hour.

    Senior Nonclinical Writer (US)

    MMS

    Canton, MI • On-site

    Full-time

    Re-posted yesterday

    Job description

    Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
     
    Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn.
    This person will participate in the development, writing, and management of highly technical nonclinical documents. This is a full-time, remote position. 

    Roles and Responsibilities:

    • Strong experience with development and writing of nonclinical documents (eg, Module 2.4 and 2.6 eCTD submission documents, 1st Edition Investigator’s Brochure [IB], Nonclinical Study Reports, Meeting Requests, Briefing Documents, RTQs).
    • Lead projects independently with minimal oversight, lead the writing (structure, content and messaging) of nonclinical submission documents for INDs/CTAs/NDAs/BLAs/MAAs, ensure the nonclinical package aligns with current regulatory guidelines and meets scientific integrity.
    • Ability to author based on highly technical sources such as GLP and non-GLP nonclinical study reports, in vivo and in vitro nonclinical data.
    • Ability to develop a mapping plan for the placement of nonclinical studies within structure of Module 2.4 and 2.6 eCTD submission documents.
    • Interpret and analyze applicable pharmacokinetics, pharmacology, and toxicology data (eg, Prism files, bioanalytical reports, clinical pathology reports, PK/TK evaluation reports).
    • Collaborate with cross-functional teams such as project management, safety, efficacy, biostats, regulatory operations, and CMC.
    • Demonstrated ability to lead others to complete complex projects.
    • Ability to complete documents according to sponsor’s format, processes, and according to regulatory guidelines.
    • Ability to effectively operate in an environment that requires negotiation, persuasion, collaboration, and analytical judgment.
    • Organizational expert within the nonclinical subject area.
    • Excellent written/oral communication and strong time and project management skills.
    • Ability to attend regular team meetings, lead client meeting and CRMs.
    • Ability to work in various client systems (eg, SharePoint, Veeva RIM, PleaseReview, EndNote), templates and toolbars.
    • Strong understanding of regulatory guidances as it applies to nonclinical submission documents and drug development (eg, ICH, FDA and EMA regulations and guidelines, GLP, GCP, GMP and GDP).

    Requirements:

    • BS + in pharmacology, toxicology, biology or chemistry, or related field, with industry experience within regulatory writing, regulatory affairs, laboratory sciences, quality assurance/control.
    • Knowledge of GLP, ICH guidelines, and applicable regulatory requirements.
    • 5+ years of pharmaceutical regulatory nonclinical writing experience.
    • Strong writing and analytical skills.
    • Proficiency with MS Office applications.   
    • Hands-on experience with clinical trial and pharmaceutical development preferred.
    • Basic understanding of CROs and scientific & nonclinical data/terminology, & the drug development process.

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    About M. M. S.

    Sourced by ZipRecruiter

    Industry

    Pharmaceutical and medicine manufacturing

    Company size

    1 - 10 Employees

    Headquarters location

    Los Angeles, CA, US

    Year founded

    1980

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