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Cmc Project Manager Jobs in Rhode Island (NOW HIRING)

... projects, 1,100+ CMC programs, and 1,397 clinical trials across all phases. Our teams are involved ... Proven experience in managing multiple tasks and adhering to timelines.Strong communication skills ...

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Cmc Project Manager information

See Rhode Island salary details

$44.1K

$102.9K

$166K

How much do cmc project manager jobs pay per year?

As of Sep 12, 2026, the average yearly pay for cmc project manager in Rhode Island is $102,853.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,300.00 and $125,800.00 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.

What are popular job titles related to Cmc Project Manager jobs in Rhode Island?

For Cmc Project Manager jobs in Rhode Island, the most frequently searched job titles are:

What cities in Rhode Island are hiring for Cmc Project Manager jobs?

Cities in Rhode Island with the most Cmc Project Manager job openings:

Infographic showing various Cmc Project Manager job openings in Rhode Island as of August 2026, with employment types broken down into 85% Full Time, 13% Part Time, and 2% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $102,853 per year, or $49.4 per hour.

Senior Scientist, Process Chemistry

Coventry, RI • On-site

Pharmaron
Chemical Manufacturing • 10K+ employees

$100K - $130K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 12 days ago


Key responsibilities

  • Lead API manufacturing technology transfer, process development, and process improvement to ensure quality and compliance.

  • Execute chemistry experiments and purification procedures to develop, improve, and validate robust API processes.

  • Identify and characterize API-related impurities and degradants to ensure product integrity.


Job description

Position: Senior Scientist, Process ChemistrySalary Range: $110,000-$130,000 Location: Coventry, RIAbout PharmaronPharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 locations in the US, UK, China, and Singapore, we support drug discovery through to manufacturing with fully integrated high-quality services.We're proud of the impact we make and just last year, we supported 887 discovery projects, 1,100+ CMC programs, and 1,397 clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,300 global customers. To learn more, visit www.pharmaron.com.Job OverviewAs a Senior Scientist, Process Chemistry you will lead and support critical aspects of API manufacturing by overseeing technology transfer, process development, and process optimization.Additional tasks:Lead API manufacturing technology transfer, process development, and process improvement to maintain and elevate high standards in quality and compliance.Oversee and document processes in alignment with cGMPs, GLP, and company policies ensuring clarity and precision.Mentor and train junior scientists and students, guiding them through best practices in process chemistry.Execute chemistry experiments and purification procedures to develop, improve and/or validate robust API processes, based on quality-by-design.Identify and characterize API-related impurities and degradants to ensure product integrity.Lead troubleshooting efforts and investigations, collaborating within cross-functional teams to optimize efficiency and resolve challenges.Present data summaries (written and oral) to communicate findings effectively within and outside your team.Communicate openly within the group to provide and gather information to optimize efficiency.Maintain good laboratory practices in compliance with safety and environmental requirements.Work independently and collaboratively to achieve both individual and team goals.Perform other related assignments and duties as required.What We're Looking For:We are seeking individuals who have strong communication skills with attention to detail who thrive in fast-paced environments.BSc + 5 years relevant pharmaceutical experienceMSc + 4 years relevant pharmaceutical experiencePhD (entry)Strong knowledge of analytical techniques (NMR, HPLC, GC, DSC, XRD) and MS Office Suite (Word, PowerPoint, Excel).Familiarity with DynoChem or other process modelling is an asset.Knowledgeable in the use of DesignExpert, JMP, Minitab or other DoE software is an asset.Proven experience in managing multiple tasks and adhering to timelines.Strong communication skills, both written and verbal.Why Pharmaron?Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 25,000 employees and operations in the US, UK, China, and Singapore. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:Comprehensive Medical, Dental & Vision Insurance with significant employer contributions401(k) Retirement Plan with generous employer matchingGenerous Paid Time Off (PTO), Paid Sick Leave & Company Holidays to support work-life balanceEmployer-funded Health Savings Account (HSA) contributions (for eligible plans), plus Healthcare & Dependent Care Flexible Spending Accounts100% Employer-paid Employee Life Insurance, AD&D, Short- and Long-Term Disability InsuranceEmployee Assistance Program (EAP), mental health resources, and wellness programsFamily-friendly benefits, including fertility support and maternity resourcesProfessional development and career growth opportunities within a leading global CRO/CDMOHow to Apply:Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.#LI-PR1