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Medical Device Liaison Jobs in Raleigh, NC (NOW HIRING)

Veranex

Sr Clinical Research Associate

Raleigh, NC · On-site

$98K - $140K/yr

... the medical device industry. Our team supports start-ups, mid-sized private companies, and the ... Acts as primary liaison to clinical sites. * Conducts site qualification visits, study start-up ...

INC Research

Biometrics Project Manager

Raleigh, NC

... and medical device industries. We do this across six continents, and we'll do it for you too ... Duties include primary liaison with Customers, Vendors, Senior Management, and/or Investigative ...

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 ... Duties include primary liaison with Customers, Vendors, Senior Management, and/or Investigative ...

IQVIA

Director, MedTech Business Development

Durham, NC · On-site

$111K - $309K/yr

Serve as a liaison between the customer and technical and operational groups at IQVIA, Inc ... medical device development Excellent analytical skills in assessing and interpreting customer ...

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All JobsMedical Device Liaison JobsMedical Device Liaison Jobs in Raleigh, NC

Medical Device Liaison information

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How much do medical device liaison jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for medical device liaison in Raleigh, NC is $22.84, according to ZipRecruiter salary data. Most workers in this role earn between $17.74 and $25.72 per hour, depending on experience, location, and employer.

What is a medical device liaison?

Medical device liaisons are professionals who act as a bridge between medical device companies and healthcare providers. They provide education, training, and support to clinicians on the safe and effective use of medical devices. Their role often includes facilitating product demonstrations, addressing technical questions, and ensuring compliance with regulatory standards. Medical device liaisons help ensure that medical professionals are informed about the latest advancements and best practices related to the devices they represent.

What are the key skills and qualifications needed to thrive as a medical device liaison?

To thrive as a Medical Device Liaison, you need a solid background in life sciences or biomedical engineering, combined with strong knowledge of medical devices and relevant regulatory requirements. Familiarity with CRM software, data analysis tools, and product-specific certifications such as those from the Regulatory Affairs Professionals Society (RAPS) are typically required. Excellent communication, relationship-building, and presentation skills help you effectively educate and support healthcare professionals. These skills ensure successful product adoption, compliance, and strong partnerships between manufacturers and clinical end-users.

What are some common challenges medical device liaisons face when working with healthcare professionals?

Medical Device Liaisons often encounter challenges such as keeping up with rapidly advancing technologies and ensuring that healthcare professionals fully understand the device's features and benefits. Building trust and maintaining effective communication with clinicians can also be demanding, especially when addressing concerns or questions about product efficacy and safety. Additionally, liaisons must navigate varying hospital protocols and manage scheduling to provide timely training and support, all while complying with strict regulatory guidelines. Successfully overcoming these challenges requires adaptability, strong interpersonal skills, and a deep understanding of both the product and the healthcare environment.

How do I become a medical device liaison?

To become a medical device liaison, candidates typically need a background in healthcare, biomedical engineering, or a related field, along with strong communication and technical skills. Relevant experience in medical device sales, regulatory affairs, or clinical support is often required, and certifications such as Regulatory Affairs Certification (RAC) can enhance prospects. Familiarity with medical device regulations and the ability to explain complex technical information to diverse audiences are essential for success in this role.

What does a medical device liaison do?

A medical device liaison acts as a bridge between medical device manufacturers and healthcare providers, ensuring proper communication, training, and support for medical devices. They often provide product education, gather user feedback, and ensure compliance with regulatory standards, typically requiring knowledge of medical regulations and strong communication skills.

What are popular job titles related to Medical Device Liaison jobs in Raleigh, NC?

For Medical Device Liaison jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Medical Device Liaison jobs in Raleigh, NC look for?

The top searched job categories for Medical Device Liaison jobs in Raleigh, NC are:

Medical Device Liaison jobs near you
Infographic showing various Medical Device Liaison job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $47,517 per year, or $22.8 per hour.

Sr Clinical Research Associate

Veranex

Raleigh, NC • On-site

$98K - $140K/yr

Other

Re-posted 10 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.
The Veranex Clinical Operations team is a dynamic group of professionals providing regulatory, quality and clinical services for the medical device industry. Our team supports start-ups, mid-sized private companies, and the largest corporations at all stages of the product life cycle. We work across a broad spectrum of technologies and treatment modalities. Our clients develop both next-generation and paradigm-shifting devices. Our product exposure includes implantables, instruments (manual, laser, robotic, etc.), capital equipment, combination products, software as a medical device (SaMD), medical mobile apps, in vitro diagnostics and more
About This Role:
Veranex has an exciting opportunity to join our team as a Senior Clinical Research Associate to support our Clinical Operations team. The Sr. CRA will participate in the planning, development, and execution of clinical trials to evaluate the safety, effectiveness and performance of medical devices. Under management supervision, the Sr. CRA will monitor assigned clinical trials to ensure adherence to the clinical protocol, applicable regulations, and company Standard Operating Procedures (SOPs) governing clinical studies.
Location: Remote, US
What You Will Do:
  • Responsible for ensuring that study investigators and coordinators comply with the study protocol, Good Clinical Practices (GCPs), Code of Federal Regulations (CFRs), and Institutional Review Board (IRB)/Ethics Committee (EC) requirements during clinical studies by training/guidance of investigators/research coordinators, conducting periodic on-site evaluations and follow-up of corrective actions
  • Acts as primary liaison to clinical sites.
  • Conducts site qualification visits, study start-up activities (essential document collection), site qualification visits, site initiation visits and training, monitoring visits for source data verification (reported study data are accurate, complete, and verifiable from source documents in the site's medical records), and site close-out visits. Generates high-quality site qualification, initiation, monitoring, and close-out visit reports in timely manner (in accordance with the Clinical Monitoring Plan)
  • Contributes to protocol, informed consent, case report form (CRF) and study plan development as well as annual progress reports (APRs) and the clinical study report (CSR) at study conclusion to report the study results to FDA and other regulatory authorities
  • Ensures that the rights and well-being of human subjects are protected and confirms data quality/integrity by maintaining site compliance, reviewing adverse events and device deficiencies, reviewing data trending/metrics, reviewing audit reports, and implementing corrective actions as necessary
  • Supports maintenance of department SOPs and work instructions
  • Supports investigational device traceability including documentation for forecasting, shipping, receipt, and disposition.
  • Supports and maintains documentation of all clinical research activities in the study trial master file (TMF), e.g., monitoring reports, site correspondence, device inventory information.
  • Drives trial enrollment and identifies and communications potential and actual obstacles to enrollment.
  • Travel requirement: 25-50%

Qualifications:
Required skills:
  • Minimum of 5 years of directly related work experience or equivalent in clinical research, including work on medical device significant risk IDE trials and/or non-significant risk abbreviated IDE trials.
  • Must be able to work autonomously and as a member of a cross-functional team and meet high expectations and tight deadlines. May work on highly visible projects in high-pressure situations
  • Must have working knowledge of Good Clinical Practices (GCPs), FDA regulations and IRB requirements.
  • Must have strong project management competencies and ability to work with high quality, reliability, and attention to detail.
  • Must have a strong level of professionalism, including verbal and written communication skills; and the ability to communicate with all levels of the organization, cross-functionally, and with clients/partners.
  • Must have proficiency in using Microsoft Office Suite, including Word, Excel, Outlook and PowerPoint; as well as experience with electronic data capture (EDC) and electronic Trial Master File (eTMF) systems.
  • Experience interfacing successfully with physicians/clinical staff and familiarity with hospital/clinical environments
  • Familiarity with medical and anatomical terminology.
  • Ability and willingness to travel

Preferred:
  • BS or BA degree preferred; BS or BA in a relevant scientific discipline or related field also preferred.

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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