ZipRecruiter

Log In

1

Cmc Project Jobs (NOW HIRING)

Icon plc

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 ...

ICON

CMC Project Manager

Blue Bell, PA · On-site +1

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 ...

next page

Showing results 1-20

All JobsCmc Project Jobs

Cmc Project information

See salary details

$13

$21

$31

How much do cmc project jobs pay per hour?

As of Jun 20, 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 jobs pay 2000 a day?

High-paying jobs that can pay around $2,000 a day often include specialized roles such as senior consultants, surgeons, or experienced project managers in certain industries. These positions typically require advanced skills, certifications, or extensive experience, and may involve freelance or contract work with high hourly rates. Such roles are usually found in finance, healthcare, or consulting sectors and may require long hours or high levels of responsibility.

What are some 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 are CMC Project managers?

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.

Are CMC jobs in high demand?

CMC (Chemistry, Manufacturing, and Controls) jobs are in steady demand within the pharmaceutical and biotech industries due to ongoing development and regulatory requirements. These roles often require knowledge of quality assurance, regulatory standards, and relevant technical skills, making them essential for product development and compliance processes.

What are CMC projects?

CMC projects refer to activities related to Chemistry, Manufacturing, and Controls in pharmaceutical development, focusing on ensuring drug quality, safety, and efficacy. These projects involve documentation, validation, and regulatory compliance, often requiring collaboration between scientists, engineers, and regulatory experts.

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 job makes $10,000 a month without a degree?

A CMC Project manager or similar project management roles in certain industries can earn $10,000 or more per month through experience and certifications like PMP. High-paying freelance or consulting roles in fields such as digital marketing, software development, or sales can also reach this income level without requiring a degree, but they typically demand strong skills and proven results.

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

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.
More about Cmc Project jobs
What are the most commonly searched types of Cmc Project jobs? The most popular types of Cmc Project jobs are:
What job categories do people searching Cmc Project jobs look for? The top searched job categories for Cmc Project jobs are:
Cmc Project jobs near you
Infographic showing various Cmc Project job openings in the United States as of June 2026, with employment types broken down into 23% Internship, 38% Full Time, 8% Part Time, and 31% Temporary. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $44,814 per year, or $21.5 per hour.
CMC Project Manager

CMC Project Manager

Icon plc

Blue Bell, PA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 18 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 requesthere.

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

Apply