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CMC Project Manager

Blue Bell, PA · On-site

CMC Project Manager ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

Uniquity Bio, Inc.

Lead cross-functional CMC project management activities for monoclonal antibody development programs from preclinical development through commercialization. * Partner with the Sr. Director ...

Eli Lilly and Company

Data Engineer

Indianapolis, IN · On-site

$109K - $131K/yr

The CMC Project Management team is responsible for leading the design and execution of integrated CMC strategies from portfolio entry through global submissions and approvals. The PAI is a newly ...

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Cmc Project information

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How much do cmc project jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for cmc project in the United States is $21.55, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $24.28 per hour, depending on experience, location, and employer.

What is a CMC project manager?

CMC Project managers oversee the Chemistry, Manufacturing, and Controls (CMC) aspects of drug development and production. They coordinate activities across various teams, ensuring that pharmaceutical products meet regulatory standards for quality, safety, and efficacy. Their responsibilities include managing timelines, budgets, documentation, and communication between research, manufacturing, and regulatory affairs. CMC Project managers play a critical role in bringing new drugs to market efficiently and compliantly.

What skills and qualifications are needed to be a CMC project manager?

To thrive as a CMC (Chemistry, Manufacturing, and Controls) Project Manager, you need expertise in pharmaceutical development, regulatory requirements, and project management, often supported by a degree in life sciences or engineering. Familiarity with tools such as project management software (e.g., MS Project), quality management systems, and regulatory submission platforms is essential. Strong organizational skills, effective communication, and cross-functional leadership are critical soft skills for coordinating complex projects and teams. These abilities ensure that CMC projects meet regulatory standards, timelines, and quality objectives, leading to successful drug development and approval.

What are common challenges faced by CMC project managers when coordinating cross-functional teams in pharmaceutical development?

CMC Project Managers often work with diverse teams, including scientists, regulatory specialists, and manufacturing experts, which can present challenges in aligning timelines, priorities, and communication styles. Navigating regulatory requirements while ensuring technical milestones are met requires strong organizational skills and proactive problem-solving. Effective CMC Project Managers facilitate clear communication, manage dependencies between functions, and adapt plans as project needs evolve, all while keeping the project on track for successful submissions.

What is the difference between Cmc Project vs Cmc Specialist?

AspectCmc ProjectCmc Specialist
CredentialsTypically requires a degree in life sciences or related field, with experience in project managementRequires a degree in chemistry, pharmacy, or related field, with knowledge of CMC regulations
Work EnvironmentInvolves managing cross-functional teams in pharmaceutical or biotech companiesFocuses on technical CMC activities, often within R&D or manufacturing settings
Industry UsageUsed in project planning, coordination, and oversight of CMC activitiesUsed in executing specific CMC tasks, data review, and regulatory submissions

The main difference is that a Cmc Project manages overall CMC activities and timelines, while a Cmc Specialist focuses on technical execution and data handling within those projects.

What are the entry level positions at CMC Project?

Entry-level positions at CMC Project typically include roles such as project coordinator, assistant project manager, or junior engineer. These roles often require basic knowledge of project management tools, strong organizational skills, and sometimes relevant certifications like OSHA or PMP for advancement.

What is CMC in project management?

In project management, CMC typically refers to Chemistry, Manufacturing, and Controls, which are essential components in pharmaceutical and biotech projects to ensure product quality and compliance. It involves planning, documentation, and validation of processes, often requiring specialized knowledge and adherence to regulatory standards. Effective CMC management helps ensure timely product development and approval.
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What are the most commonly searched types of Cmc Project jobs?

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Cmc Project jobs near you
Infographic showing various Cmc Project job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 85% Full Time, 10% Part Time, and 3% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $44,814 per year, or $21.5 per hour.

CMC Project Manager

Blue Bell, PA • On-site

842 ICON Clinical Research Belgium BV
See more jobs at 842 ICON Clinical Research Belgium BVexternal

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 27 days ago

Job description

CMC Project Manager

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


As a Senior Manager, Regulatory Affairs at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

Your focus will be on overseeing regulatory affairs delivery, coaching your team, and driving continuous improvement.
Key responsibilities include:

  • Participate in provision of regulatory expertise in strategic drug development across multiple areas.
  • Take part in preparation of strategic development and submission plans.
  • Be involved in the regulatory affairs activities across the ICON portfolio and be an expert and advisor to ICON clients (externally and internally).
  • Be a trusted partner - represent the Regulatory Affairs Department in business development activities and generate new business opportunities.
  • Contribute to at least two of the following areas: interactions with regulatory agencies, early phase consulting, development planning (PDP/RDP/CDP), scientific/agency advice, orphan drugs/pediatric development, medical devices

Your Profile:

You will have a strong background in regulatory affairs, with proven management experience and a commitment to quality delivery.
Required qualifications and experience:

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • EU/APAC: In-depth proven regulatory affairs expertise. Minimum of 7 years' experience, supervisory experience, and pharmaceutical/CRO industry experience.
  • US/LATAM/CAN: A minimum of 7 years regulatory affairs experience including supervisory experience and a minimum of 6 years pharmaceutical/CRO industry.
  • Demonstrable experience within regulatory affairs, including development of regulatory strategies, document writing, marketing authorization applications, clinical trials, post-licensing activities, and direct regulatory agency interaction.
  • Strong organizational skills, ability to manage multiple tasks, and meticulous attention to detail.
  • Excellent written, verbal, and management skills, as well as demonstrated presentation skills, problem-solving ability, strong interpersonal skills, and the ability to plan/organize.

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply