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Project Manager Pharmaceutical Internship Jobs in Raleigh, NC

INC Research

Biometrics Project Manager

Raleigh, NC · On-site

... for the world's pharmaceutical, biotech and medical device industries. We do this across six ... Works in the role of a project manager on assigned project(s), which may range from single service ...

INC Research

Biometrics Project Manager

Raleigh, NC · On-site

... for the world's pharmaceutical, biotech and medical device industries. We do this across six ... Works in the role of a project manager on assigned project(s), which may range from single service ...

Salas O'Brien, Inc.

Project Manager

Raleigh, NC · On-site

$80 - $100/hr

Job Summary The Project Manager will lead and support execution of capital projects within regulated manufacturing environments, including pharmaceutical and life sciences facilities operating under ...

ECBuild

Construction Project Manager

Raleigh, NC · On-site

The Project Manager 2 position is responsible for the overall direction, supervision and daily ... Pharmaceutical, Healthcare, Laboratory, MEP and Commercial Experience is a plus Additional ...

ECBuild LLC

Construction Project Manager

Raleigh, NC · On-site

The Project Manager 2 position is responsible for the overall direction, supervision and daily ... Pharmaceutical, Healthcare, Laboratory, MEP and Commercial Experience is a plus Additional ...

Valspec

Project Manager - North Carolina

Raleigh, NC · On-site

Raleigh-Durham, NC About the Role We are hiring a Commissioning Project Manager to lead commissioning, qualification, and validation projects within pharmaceutical and biotech manufacturing ...

Siemens Mobility

Project Manager

Wendell, NC · On-site

$80 - $100/hr

Project management or engineering internship or related work experience in Power distribution industry. * Basic knowledge and understanding of power distribution; ability to read and understand basic ...

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Project Manager Pharmaceutical Internship information

See Raleigh, NC salary details

$19.4K

$33.4K

$45.2K

How much do project manager pharmaceutical internship jobs pay per year?

As of Sep 8, 2026, the average yearly pay for project manager pharmaceutical internship in Raleigh, NC is $33,431.00, according to ZipRecruiter salary data. Most workers in this role earn between $29,200.00 and $34,000.00 per year, depending on experience, location, and employer.

What does a project manager pharmaceutical intern do?

A Project Manager Pharmaceutical Intern supports project managers in planning, coordinating, and monitoring pharmaceutical projects. Their tasks often include tracking project timelines, assisting with documentation, preparing reports, and helping to ensure that regulatory requirements are met. Interns may also participate in meetings, collaborate with cross-functional teams, and contribute to process improvements. This internship provides hands-on experience in managing drug development or clinical trial projects within the pharmaceutical industry.

What are the key skills and qualifications needed to thrive as a project manager pharmaceutical intern?

To thrive as a Project Manager Pharmaceutical Intern, you need a background in life sciences or pharmacy, strong organizational skills, and foundational knowledge of project management principles. Familiarity with Microsoft Project, Excel, and regulatory compliance systems, as well as any coursework or certification in project management (such as CAPM), is highly beneficial. Outstanding communication, attention to detail, and adaptability will set you apart when coordinating cross-functional teams and timelines. These skills ensure you can effectively manage project deliverables, support compliance, and contribute to the successful development of pharmaceutical products.

What are popular job titles related to Project Manager Pharmaceutical Internship jobs in Raleigh, NC?

For Project Manager Pharmaceutical Internship jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Project Manager Pharmaceutical Internship jobs in Raleigh, NC look for?

The top searched job categories for Project Manager Pharmaceutical Internship jobs in Raleigh, NC are:

Project Manager Pharmaceutical Internship jobs near you
Infographic showing various Project Manager Pharmaceutical Internship job openings in Raleigh, NC as of September 2026, with employment types broken down into 82% Full Time, 16% Part Time, and 2% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $33,431 per year, or $16.1 per hour.

Biometrics Project Manager

Raleigh, NC • On-site

INC Research
Scientific Research and Development Services • 10K+ employees
Learn more about INC Researchexternal

Full-time

Re-posted 5 days ago

Syneos Health rating

8.4

Company rating: 8.4 out of 10

Based on 23 frontline employees who took The Breakroom Quiz

23rd of 86 rated pharmaceutical

Job description

Company Description
INC Research is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world's pharmaceutical, biotech and medical device industries. We do this across six continents, and we'll do it for you too.
Job Description
Ensures the contracted services and expectations of a clinical study are carried out by the Company project team in accordance with the executed contract and the Customer's expectations. Works in the role of a project manager on assigned project(s), which may range from single service studies to large full scope biometrics projects. Duties include primary liaison with Customers, Vendors, Senior Management, and/or Investigative Sites.
Essential Functions:
  • Acts as a primary liaison between the Company and the Customer to ensure study launch, conduct, and closeout according to the Customer's and Company's contractual agreement. Ensures the study is progressing according to internal and Customer quality standards, Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs), and International Conference on Harmonization (ICH) guidelines to fulfill all federal and local regulations.
  • Serves as the team leader by overseeing the biometrics project team. Facilitates team building and communication. Acts as a liaison and facilitator between other departments within the Company for project related tasks and/or issues. Plans and projects resources required across all areas for studies.
  • Manages multiple projects ranging in size and complexity from single service studies to large full scope biometrics projects, global projects and/or programs, with minimal interaction from supervisor. This includes management of resources, tasks, risk, and quality.
  • Manages the executed contract and financial aspects of assigned projects/programs as needed. Ensures customers are invoiced in a timely manner and follows up on receipt of payment as needed.
  • Maintains effective communication with the Customer and project team through oral and written correspondence, project status reports, and monthly progress reports, and ensures adequate documentation of each communication.
  • Independently prepares information for internal review meetings.
  • Maintains and evaluates project progress by maintaining timelines and other tracking/analysis tools. Produces and distributes status, resourcing, and tracking reports as well as functional area plan, to appropriate team members and senior management.
  • Networks to acquire new and/or repeat business.
  • Supports the Business Development Department by providing information on the Company Biometrics capabilities. Presents Company capabilities as well as project management specific responsibilities at Customer proposal defense meetings
  • Works with Business Development and the Proposal/Contracts groups to develop proposals for Customer requested opportunities as needed. Works with this team to develop budgets and scope of work for the final contract as needed.

Other Responsibilities:
  • Represents the Company at professional meetings or seminars.
  • May develop and refine project management processes within the Company.
  • Performs other work-related duties as assigned.
  • May develop and/or review SOPs and WIs related to any area concerning biometrics project management.
  • May develop and refine processes within the Company which lead to greater efficiencies or competitive advantages over other companies.
  • Minimal travel may be required (up to 50%).

Qualifications
Requirements:
BA/BS in life sciences, communications, nursing, or equivalent related education and experience. Project management experience in a contract research organization, pharmaceutical, or biotechnology company. Experience actively managing clinical research projects across biometrics functional areas. Previous CRO experience and specific biometrics management experience. Other relevant experience preferred. Thorough knowledge of FDA regulations, drug development, and project management procedures. Demonstrated proficiency with ICH/GCP guidelines. Strong presentation, documentation, and interpersonal skills as well as a team-oriented approach. Proficient computer skills in Word, Excel, PowerPoint, MS Project, email and internet. Flexibility and ability to handle multiple tasks to meet deadlines while delivering high quality work in a dynamic environment.
Disclaimer:
Tasks,duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities.
Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment
of its employees.
Additional Information
Why choose us?
It takes skill and passion to develop medicines the way we do. Don't worry - if you've got the passion part, we'll help you develop the skills you need to enhance every aspect of your career in the clinical research industry.
We've got an attitude at INC: "Can do, I own it." Absolutely everyone has ownership of what they do here. And because we're given the freedom and responsibility to really own our projects, we can take them to new levels. And that means we can take our careers wherever we want them, too.
"We were ranked "Top CRO" to work with in the CenterWatch 2013 Investigative Site Relationship Survey (a biannual survey of over 2,000 sites worldwide)."
What happens next?
If your application is successful you will be contacted by one of our dedicated recruiters who will arrange a suitable date and time to speak to you further about this opportunity.

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