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Imaging Project Manager Jobs in Raleigh, NC (NOW HIRING)

Fujifilm

Senior Submissions Coordinator

Durham, NC · On-site

... project coordinator/manager. * Five (5) or more years work experience in Medical Informatics or Software related industry. * Understand medical imaging terminology, workflow, and its relationship ...

Fujifilm

Senior Submissions Coordinator

Durham, NC · On-site

... project coordinator/manager. * Five (5) or more years work experience in Medical Informatics or Software related industry. * Understand medical imaging terminology, workflow, and its relationship ...

US Radiology Specialists

Senior Accountant

Raleigh, NC · On-site

$71K - $90K/yr

Prepare monthly financial statements, management reports, and supporting schedules. * Assist with ... Seasonal overtime expected (quarter-end, year-end, special projects). Lumexa Imaging provides a ...

US Radiology Specialists

AI Solutions Architect

Raleigh, NC · On-site

$61.25 - $80.75/hr

Lumexa Imaging is one of the country's largest providers of outpatient medical imaging. With over 5 ... Contribute to and help manage the AI project pipeline and prioritization process * Workflow ...

Duke University

LAB RESEARCH ANALYST I

Durham, NC · On-site

$51K - $77K/yr

Be Bold. What You'll Do: - Develop software control and user interfaces for custom laboratory imaging devices. - Utilize Python, C++, hardware control, and project management skills. - Support ...

Duke University

LAB RESEARCH ANALYST I

Durham, NC

$51K - $77K/yr

Be Bold.What You'll Do: - Develop software control and user interfaces for custom laboratory imaging devices. - Utilize Python, C++, hardware control, and project management skills. - Support ...

Danaher

Senior Software Engineer - USA Remote

Raleigh, NC · Remote

$119K - $157K/yr

... imaging, and analysis, unveiling the invisible and empowering our customers to build a better ... Here, you will work on meaningful projects alongside passionate colleagues, driving progress and ...

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Imaging Project Manager information

See Raleigh, NC salary details

$37.4K

$99.8K

$157.5K

How much do imaging project manager jobs pay per year?

As of Jun 18, 2026, the average yearly pay for imaging project manager in Raleigh, NC is $99,815.00, according to ZipRecruiter salary data. Most workers in this role earn between $76,300.00 and $119,600.00 per year, depending on experience, location, and employer.

How does an Imaging Project Manager typically collaborate with cross-functional teams during a project?

Imaging Project Managers often work closely with radiologists, IT professionals, and clinical staff to ensure successful implementation of imaging projects. They facilitate communication between technical and medical teams, manage project timelines, and address any workflow or integration challenges that arise. Regular meetings and status updates are common, and the Imaging Project Manager is responsible for aligning project goals with departmental needs while ensuring compliance with healthcare regulations.

What is the difference between Imaging Project Manager vs Radiology Technologist?

AspectImaging Project ManagerRadiology Technologist
Required CredentialsProject management certification, healthcare or imaging industry knowledgeRadiologic technologist license, ARRT certification
Work EnvironmentHealthcare facilities, imaging departments, project settingsHospitals, clinics, diagnostic imaging centers
Employer & Industry UsageHospitals, healthcare organizations, imaging service providersMedical imaging departments, radiology clinics
Common Search & Comparison IntentUnderstanding roles in healthcare imaging projectsTechnical radiology procedures and patient care

The Imaging Project Manager oversees imaging projects, coordinating teams and resources, often requiring project management credentials. In contrast, a Radiology Technologist performs diagnostic imaging procedures, requiring specialized technical certifications. While both roles work within healthcare imaging environments, their responsibilities and qualifications differ significantly.

What does an Imaging Project Manager do?

An Imaging Project Manager oversees the planning, coordination, and execution of imaging-related projects, such as medical imaging, digital asset management, or photographic archives. They work with cross-functional teams to ensure imaging projects are completed on time, within budget, and to the required quality standards. Their responsibilities often include managing resources, communicating with stakeholders, and troubleshooting technical issues related to imaging systems or processes.

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

To thrive as an Imaging Project Manager, you need expertise in project management, a strong understanding of imaging technologies, and a relevant degree in fields such as radiology, engineering, or information technology. Familiarity with project management software (like MS Project or Asana), imaging modalities (such as MRI, CT, or PACS), and certifications like PMP are highly beneficial. Excellent leadership, organizational, and communication skills help manage cross-functional teams and client expectations. These abilities are crucial for delivering complex imaging projects on time, within scope, and to high technical standards.
What are popular job titles related to Imaging Project Manager jobs in Raleigh, NC? For Imaging Project Manager jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Imaging Project Manager jobs in Raleigh, NC look for? The top searched job categories for Imaging Project Manager jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Imaging Project Manager jobs? Cities near Raleigh, NC with the most Imaging Project Manager job openings:
Imaging Project Manager jobs near you
Infographic showing various Imaging Project Manager job openings in Raleigh, NC as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $99,815 per year, or $48 per hour.
Senior Submissions Coordinator

Senior Submissions Coordinator

Fujifilm

Durham, NC • On-site

Other

Posted 8 days ago

Fujifilm rating

8.3

Company rating: 8.3 out of 10

Based on 66 frontline employees who took The Breakroom Quiz

46th of 518 rated manufacturers

Job description

Position Overview
This position is intended to provide technical documentation and Submissions expertise and support to all FUJIFILM Healthcare Americas Corporation (HCUS) business sites. A Submissions Coordinator plays a crucial role in ensuring that products meet regulatory standards and facilitates the submission process to regulatory agencies such as but not limited to U.S. Food and Drug Administration (U.S. FDA) and European regulatory agencies under the EU Medical Device Regulation (EU MDR) - Regulation (EU) 2017/745.
This position provides technical documentation as required by U.S. Food and Drug Administration (U.S. FDA) and European regulatory agencies under the EU Medical Device Regulation (EU MDR) - Regulation (EU) 2017/745.
As a Senior this position will lead and manages projects that aim to be submitted to U.S. Food and Drug Administration (U.S. FDA) and European regulatory agencies under the EU Medical Device Regulation (EU MDR) - Regulation (EU) 2017/745.
Company Overview
At FUJIFILM Healthcare Americas Corporation, we're on a mission to innovate for a healthier world, and we need passionate, driven people like you to help us get there. Our cutting-edge healthcare solutions span diagnostic imaging, enterprise imaging, endoscopic and surgical imaging, as well as in-vitro diagnostics.
But we don't stop at healthcare; our Non-Destructive Testing (NDT) team harnesses advanced radiography solutions to keep transportation infrastructure, aerospace, and oil and gas assets safe and running smoothly.
Ready to innovate, collaborate, and make a difference? Join us and bring your big ideas to life while working in a dynamic, flexible environment that fuels your creativity and drive.
Our headquarters is in Lexington, Massachusetts, an inspiring healthcare research hub in a historic town.
Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of "giving our world more smiles." Visit: https://www.fujifilm.com/us/en/about/region/careers
Job Description
Duties and responsibilities
  • Document Preparation and Submission: The coordinator is responsible for preparing and submitting technical documentation to agencies such as the FDA or European regulatory agencies. This includes ensuring that all submissions are complete, accurate, and compliant with applicable regulations.
    • Document Preparation:
      • Develop and maintain detailed Software Requirements Specification that is required to meet internal and regulatory needs.
      • Facilitate the creation, create or maintain Software Architecture and Software Design Specifications (SDS) in coordination with the Design and Development teams. SDSs must meet internal and regulatory needs.
      • Create and maintain performance data in conjunction with AI Developers that is required to meet regulatory needs.
      • Create and maintain Technical Documentation required by EU MDR - Regulation (EU) 2017/745, U.S. FDA and other regulatory regions.
    • Submission:
      • Coordinate and complete U.S. FDA pre-market submissions (510(k) and PMA) in accordance with the HCUS business plan.
      • Maintain the U.S. FDA database for Establishment Registrations and Device Listings for all FUJIFILM business entities.
      • Coordinate and complete submissions under the EU MDR - Regulation (EU) 2017/745 in accordance with the HCUS business plan. Prepare European Union Technical Documentation and International Regulatory Submissions.
    • Provide support for International Registrations, as needed.
  • Submission Projects: The Senior Submissions Coordination is responsible for managing submission projects. This includes:
    • Create and manage the project schedule and task details.
    • Ensure the submission projects stay on schedule.
    • This individual must be able to track and support multiple simultaneous projects, keep all stakeholders appraised of status and issues, perform risk analysis and create risk mitigation strategies.
    • Ability to work with and manage cross functional projects simultaneously
    • Cross-Department Collaboration: A submission coordinator works closely with various departments, including research and development, quality assurance, regulatory, and legal teams, to gather necessary information and ensure compliance throughout the product lifecycle.
  • Liaise with the HCUS RA/QA department to ensure that there is open communication and to assist with all RA/QA needs relating to the Company's software registration, regulatory-related audits, and other issues that arise from time-to-time.
  • Compliance Monitoring: The coordinator must stay updated on evolving regulations and ensure that the organization adheres to these standards. This involves maintaining meticulous records and facilitating communication between the organization and regulatory bodies.
  • Risk Management: The coordinator plays a role in strategizing regulatory pathways and managing risks associated with product approvals and compliance.
  • Coordinate U.S. Import/Export/Customs related activities.
  • Interact closely with Customer Service, Service, Repair, Research and Development, Quality Assurance, Regulatory Affairs and Sales to facilitate required action.
  • Support and provide evidence for Internal Audits and External Audits.
  • Create and/or update Standard Operating Procedures and Work Instructions.
  • Perform Corrective and Preventive Action activities as assigned.
  • Attend all department and company-wide team meetings as needed.
  • Other duties as assigned.
  • Comply with all applicable U.S. Food and Drug Administration (U.S. FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all other applicable laws, regulations, and standards.

Qualifications
  • Bachelor's Degree required.
    • Bachelor's degree in computer science, Software Development, Information Technology or similar preferred.
  • Experience documenting complex Software Systems.
  • Prior experience as a developer, quality assurance technical writer for MI products or project coordinator/manager.
  • Five (5) or more years work experience in Medical Informatics or Software related industry.
  • Understand medical imaging terminology, workflow, and its relationship with HCUS products.
  • Three (3) or more years of hands-on experience working in a regulated environment and supporting the Regulatory Affairs department.
  • Excellent project management, communication, collaboration, teamwork, interpersonal, problem solving and critical thinking skills.
  • Understand Software terminology and techniques with the ability to translate software concepts to meet regulatory needs.
  • Expert and Strong computer skills Microsoft project management application (Excel, Word, PowerPoint, TFS, MS Project. etc.).
  • Knowledge of U.S. FDA medical device regulations (21 CFR 820, 21 CFR 803, 21 CFR 806, 21 CFR 807) and U.S. FDA import/export/customs regulations.
  • Knowledge of international medical device standard requirements (ISO 13485/ISO 9001, ISO 14971, EU Medical Device Directive and Canada Medical Device Regulations).
  • Excellent written and verbal communication skills.
  • Strong ability to multi-task and to meet business deadlines.
  • Excellent organizational skills with an ability to think proactively and prioritize work.
  • Prior knowledge of Medical Informatics Medical Devices (Software Devices)
    • Ability to learn and master new software products.
    • Prior knowledge with HCUS MI products is a plus.

Physical requirements
The position requires the ability to perform the following physical demands and/or have the listed capabilities:
  • The ability to sit up 75-100% of applicable work time.
  • The ability to use your hands and fingers to feel and manipulate items, including keyboards, up to 100% of applicable work time.
  • The ability to stand, talk, and hear for 75% of applicable work time.
  • The ability to lift and carry up to ten pounds up to 20% of applicable work time.
  • Close Vision: The ability to see clearly at twenty inches or less.

Travel
  • Occasional (up to 25%) travel may be required based on business need.

In the event that COVID-19 vaccine mandates issued by the federal government, or by state or local government become effective and enforceable, the Company will require that the successful candidate hired for positions covered under relevant government vaccine mandate(s) be fully vaccinated against COVID-19, absent being granted an accommodation due to medical or sincerely held religious belief or other legally required exemption.
Applicants to positions where vendor credentialing or other similar requirements exist to enter facilities will be required to comply with the credentialing requirements of the facilities, including complying with vaccine requirements.
For all positions, the Company encourages vaccination against COVID-19 and requires that the successful candidate hired be willing to test for the COVID-19 virus periodically and wear a face covering indoors as required, absent being granted an accommodation due to medical or sincerely held religious belief or other legally required exemption.
EEO Information
Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.
ADA Information
If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (hcushr.department@fujifilm.com or (330) 425-1313).

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About Fujifilm

Sourced by ZipRecruiter

With each Industry we enter, We’ve learned to Leverage and Adapt our knowledge, Expertise and rRsources to make the World a better place. When it comes to Innovating for a Healthier World and a more sustainable society, we’ll NEVER STOP. Fujifilm will contribute to the social challenges by creating new value in a wide range of business domains through innovation in Products, Services, and Technological Development. We launched our Healthcare Business with X-ray film in 1936. And now, We are developing our business in areas of prevention, diagnosis, and treatment as a Comprehensive Healthcare Company. We will never stop Innovating for a Healthier World.

Industry

Chemical manufacturing

Company size

10,000+ Employees

Headquarters location

Minato-ku, Tokyo, JP

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