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

Hired by Matrix

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Sales Support Professional

Cary, NC · On-site

$33.43/hr

Are you ready to build your career by joining a multi-national medtech company? If so, our client ... both customer side and sales or project management organization. * Initiates sales orders ...

Millennium Physician Group

Laboratory MedTech Lead

Durham, NC · On-site

$18.25 - $24.50/hr

Document findings meticulously for review by laboratory management and healthcare providers. • ... special projects and initiatives as required to support laboratory operations and continuous ...

Jj

Learning Experience Lead

Raleigh, NC · On-site

Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate ... Experience with project management tools (MS Project, Planner, Asana, Monday.com or similar ...

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All JobsMedtech Project Manager JobsMedtech Project Manager Jobs in Raleigh, NC

Medtech Project Manager information

See Raleigh, NC salary details

$37.4K

$99.8K

$157.5K

How much do medtech project manager jobs pay per year?

As of Jun 27, 2026, the average yearly pay for medtech 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.

What does a Medtech Project Manager do?

A Medtech Project Manager oversees the planning, execution, and delivery of projects related to medical technology, such as the development of medical devices or healthcare software. They coordinate cross-functional teams, manage timelines and budgets, and ensure compliance with regulatory standards. Their role is crucial in bridging the gap between technical development, clinical requirements, and business goals to bring innovative medical solutions to market efficiently and safely.

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

To thrive as a Medtech Project Manager, you need a strong background in project management, biomedical engineering or life sciences, and a solid understanding of regulatory requirements, often supported by a relevant degree and PMP or similar certification. Familiarity with project management software like MS Project or Jira, as well as knowledge of FDA/CE regulations and quality management systems, is typically required. Exceptional leadership, communication, and problem-solving skills help drive cross-functional teams and manage stakeholder expectations. These abilities ensure timely product development, regulatory compliance, and successful project outcomes in the highly regulated Medtech industry.

How does a Medtech Project Manager typically collaborate with cross-functional teams during the product development lifecycle?

A Medtech Project Manager frequently works with cross-functional teams, including R&D, regulatory affairs, quality assurance, marketing, and manufacturing. They coordinate efforts by facilitating regular meetings, setting clear timelines, and ensuring all team members are aligned with project goals and compliance requirements. Strong communication skills are essential, as the Project Manager must translate technical updates between departments and resolve potential roadblocks promptly. This collaborative approach helps deliver innovative medical technologies efficiently while meeting regulatory standards.

What is the difference between Medtech Project Manager vs Medical Device Engineer?

AspectMedtech Project ManagerMedical Device Engineer
Required credentialsBachelor's in engineering, project management certification (PMP)Bachelor's or higher in biomedical, mechanical, or electrical engineering
Work environmentProject teams, cross-functional collaboration, client interactionsDesign, development, testing, and manufacturing of medical devices
Employer & industry usageMedical device companies, healthcare tech firmsMedical device manufacturing, R&D departments
Common search & comparison intentUnderstanding project management roles in medtechTechnical engineering roles in medical device development

The Medtech Project Manager focuses on overseeing medical device projects, coordinating teams, and ensuring timely delivery. In contrast, a Medical Device Engineer is primarily involved in designing, developing, and testing medical devices. Both roles require engineering backgrounds, but their daily tasks and responsibilities differ significantly, catering to different aspects of the medical device lifecycle.

What are popular job titles related to Medtech Project Manager jobs in Raleigh, NC? For Medtech Project Manager jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Medtech Project Manager jobs in Raleigh, NC look for? The top searched job categories for Medtech Project Manager jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Medtech Project Manager jobs? Cities near Raleigh, NC with the most Medtech Project Manager job openings:
Medtech Project Manager jobs near you
Infographic showing various Medtech Project Manager job openings in Raleigh, NC as of June 2026, with employment types broken down into 86% Full Time, 10% Part Time, 1% Temporary, and 3% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $99,815 per year, or $48 per hour.
Sr/Clinical Proposal Strategy Manager

Sr/Clinical Proposal Strategy Manager

Veranex

Raleigh, NC • On-site

Full-time

Posted 11 days ago

Job description

Veranex's mission as an Innovation CRO is to improve patient outcomes by accelerating our clients' innovations to market. As the world's only end-to-end professional services firm focused on MedTech, we take clients' Vision to Velocity through our comprehensive service portfolio, with expertise in human centered design and product development, preclinical and clinical research, regulatory affairs, and market access and reimbursement consulting.
About This Role:
Veranex is seeking a Clinical Proposal Strategy Manager / Senior Manager to support high-impact clinical business development efforts within our Global Clinical Affairs organization.
In this role, you will serve as a central driver of proposal strategy, translating complex clinical trial requirements into competitive, executable, and client-focused proposals. You will partner cross-functionally with Clinical Operations, Business Development, Clinical Data Services, and Subject Matter Experts (SMEs) to develop robust study strategies, timelines, and budgets.
This is a high-visibility, client-facing role that blends clinical expertise, operational planning, and commercial acumen-ideal for individuals who thrive at the intersection of strategy and execution in the MedTech clinical CRO space.
What You Will Do:
  • Lead and facilitate execution strategies and planning content for clinical trial programs for inclusion in Business Development proposals.
  • Translate RFPs into specific deliverables with supporting project execution strategy, budget, milestones, and timeline.
  • Manage, lead, and facilitate inclusion of Subject Matter Expert content into the proposal execution strategy.
  • Capture and communicate strategic assumptions, risks, and key budget drivers fundamental to the execution strategy.
  • Work closely with Business Development to define compelling strategies, support client positioning, and align solutions to client needs.
  • Present execution strategy details to clients in support of Business Development.
  • Serve as the lead clinical SME for clinical proposal development opportunities, providing strategic guidance on study design, operational feasibility, regulatory requirements, and industry standards.
  • Translate protocols, schedules of events (SOEs), and clinical requirements into executable proposal strategies and project plans.
  • Develop accurate, competitive clinical budgets based on scope, visit schedules, assumptions, and third-party costs.
  • Partner with internal stakeholders to ensure budgets and project plans are executable, compliant, and commercially sound.
  • Participate in client calls to clarify needs, align approach, and strengthen confidence in Veranex's clinical capabilities.
  • Partner with global SMEs and service line leaders to gather and refine technical and operational proposal content.
  • Collaborate with Proposal Specialists to ensure proposal content is complete, compliant, and submission ready.
  • Lead internal proposal strategy meetings and kickoffs for Clinical opportunities.
  • Support alignment between proposal strategy and downstream study execution expectations.
  • Identify, evaluate, and help establish relationships with key clinical vendors and partners.
  • Support development of internal guidelines, templates, and tools for optimizing clinical study proposal development.
  • Contribute to the growth of Veranex's clinical text repository, experience database, and reusable content library.
  • Help drive continuous improvement of clinical proposal templates, budget tools, and strategic messaging.

Qualifications:
Manager Level - Required
  • Bachelor's degree in life sciences, clinical research, healthcare, or related medical/technical field
  • 5+ years of experience in clinical research operations, and/or clinical proposal development within a CRO, with exposure to medical device or MedTech studies
  • Foundational understanding of clinical trial lifecycle, including study design, execution, and regulatory requirements
  • Experience interpreting protocols, schedules of events (SOEs), and scopes of work
  • Ability to translate clinical and operational inputs into structured proposal strategies and plans
  • Experience working in cross-functional environments and supporting proposal development efforts
  • Strong organizational, communication, and problem-solving skills
  • Ability to manage multiple priorities in a fast-paced, deadline-driven environment

Manager Level - Preferred
  • Experience supporting proposal development in a CRO or consulting environment
  • Exposure to medical device regulatory pathways (e.g., 510(k), IDE, CE Mark)
  • Experience with clinical trial budgeting and vendor coordination
  • Strong focus on medical device studies

Senior Manager Level - Required
  • Bachelor's degree in life sciences, clinical research, healthcare, or related field
  • 8+ years of experience in clinical research, clinical operations, and/or proposal development within a CRO
  • Deep understanding of end-to-end clinical trial strategy, planning, and execution
  • Proven experience leading cross-functional proposal development
  • Demonstrated ability to translate complex protocols, RFPs, and client requirements into fully executable and competitive proposal strategies
  • Strong experience developing and validating clinical budgets, timelines, and resource assumptions
  • Experience operating in FDA-regulated and ISO-compliant environments
  • Advanced communication and presentation skills, including client-facing interactions and proposal defenses
  • Strong business acumen and ability to balance scientific rigor with commercial considerations

Senior Manager Level - Preferred
  • Advanced degree (MS, MPH, MBA, or PhD) in life sciences or related discipline
  • Experience within a MedTech CRO, professional services, or consulting environment
  • Strong focus on medical device studies
  • Experience supporting regulatory submissions (e.g., 510(k), PMA, IDE, CE Mark)
  • Experience leading complex, multi-stakeholder programs or global studies
  • Familiarity with vendor ecosystems and external partner strategy in clinical trials

Veranex is an equal opportunity employer and prohibits discrimination of any kind. All qualified applicants will receive consideration for employment without regard for race, color, religion or belief, sex (including pregnancy, gender identity or gender expression), sexual orientation, parental or marital status, disability, age, status as a protected veteran, national, social, or ethnic origin, or any other applicable legally protected characteristics.

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