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Seasonal Medical Device Project Manager Jobs in Raleigh, NC

INC Research

Biometrics Project Manager

Raleigh, NC · On-site

... and medical device industries. We do this across six continents, and we'll do it for you too ... Works in the role of a project manager on assigned project(s), which may range from single service ...

GSK

Senior Device Quality Engineer

Zebulon, NC · On-site

$75K - $101K/yr

... medical devices within combination products. Responsibilities include risk management ... You will have opportunities to lead projects, broaden technical skills, and influence quality ...

CTI

Clinical Project Coordinator

Raleigh, NC · On-site

Support Clinical Project Manager / Director in completing clinical project management activities ... and medical device firms. For more information, visit www.ctifacts.com Why CTI? * Advance Your ...

CTI

Clinical Project Coordinator

Raleigh, NC · On-site

Support Clinical Project Manager / Director in completing clinical project management activities ... and medical device firms. For more information, visit www.ctifacts.com Why CTI? * Advance Your ...

Eisai

Mgr., Product Complaints (Hybrid)

Raleigh, NC · Hybrid

$104K - $137K/yr

This role ensures that medical device complaints are consistently captured, appropriately triaged ... Manage complaint sample handling (shipping, tracking) to external sites for investigation. * Review ...

Cree

NTI Project Manager

Durham, NC

As a Project Manager in the NTI PMO Group, you will be responsible for the project management and ... Develop and utilize models to accurately predict power product device performance * Own life cycle ...

WolfSpeed Inc.

NTI Project Manager

Durham, NC · On-site

As a Project Manager in the NTI PMO Group, you will be responsible for the project management and ... Develop and utilize models to accurately predict power product device performance * Own life cycle ...

Medical Leverage

Project Manager

Cary, NC · On-site

Description At medical leverage we are passionate about improving life through communications. We ... Manage changes to the project scope, schedule, and budget * Manage and coordinate internal ...

Medical Leverage

Project Manager

Cary, NC · On-site +1

As part of the Medical Leverage team, the Project Manager will be the main point of contact with the client. You will lead the planning and implementation of projects by owning a detailed timeline ...

Wolfspeed, Inc.

NTI Project Manager

Durham, NC · On-site

As a Project Manager in the NTI PMO Group, you will be responsible for the project management and ... Develop and utilize models to accurately predict power product device performance * Own life cycle ...

PM Group

Project Engineer III

Apex, NC · On-site

$75K - $98K/yr

Experience working in a highly regulated environment such as Pharma, Medical Device, or Semi ... Project Management Professional (PMP) or Professional Engineer (PE) license is preferred but not ...

PM Group

Project Engineer III

Apex, NC · On-site

$75K - $98K/yr

Experience working in a highly regulated environment such as Pharma, Medical Device, or Semi ... Project Management Professional (PMP) or Professional Engineer (PE) license is preferred but not ...

Elmington

Project Manager

Raleigh, NC · On-site

As a Project Manager at Elmington Construction, you will deliver projects according to their plans ... Temperature in the workplace is typically moderate, though the ability to withstand seasonal cold ...

Elmington

Project Manager

Raleigh, NC · On-site

As a Project Manager at Elmington Construction, you will deliver projects according to their plans ... Temperature in the workplace is typically moderate, though the ability to withstand seasonal cold ...

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Seasonal Medical Device Project Manager information

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How much do seasonal medical device project manager jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for seasonal medical device project manager in Raleigh, NC is $51.75, according to ZipRecruiter salary data. Most workers in this role earn between $40.19 and $63.80 per hour, depending on experience, location, and employer.

What is the difference between Seasonal Medical Device Project Manager vs Medical Device Quality Assurance Specialist?

AspectSeasonal Medical Device Project ManagerMedical Device Quality Assurance Specialist
CredentialsProject management certification (PMP), relevant industry experienceISO 13485 training, quality assurance certifications
Work EnvironmentProject teams, manufacturing sites, regulatory agenciesQuality departments, laboratories, compliance offices
Employer & Industry UsageMedical device companies during peak seasons or product launchesManufacturers ensuring product quality and regulatory compliance
Search & Comparison IntentUnderstanding project management roles in medical device industryQuality assurance roles and compliance responsibilities

The Seasonal Medical Device Project Manager focuses on managing projects during specific seasons or product launches, coordinating teams, and ensuring timely delivery. In contrast, the Medical Device Quality Assurance Specialist concentrates on maintaining product quality, compliance with regulations, and conducting audits. Both roles require industry-specific certifications and work within the medical device manufacturing environment, but their core responsibilities differ significantly.

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Seasonal Medical Device Project Manager jobs near you

Biometrics Project Manager

INC Research

Raleigh, NC • On-site

Full-time

Re-posted 16 days ago

Syneos Health rating

8.1

Company rating: 8.1 out of 10

Based on 22 frontline employees who took The Breakroom Quiz

38th 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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