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Medical Device Clinical Research Manager Jobs in Raleigh, NC

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 ... Under management supervision, the Sr. CRA will monitor assigned clinical trials to ensure adherence ...

Duke University

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

Ranked sixth among medical schools in the nation, the School takes pride in being an inclusive ... Coordinate and manage complex clinical research studies, including drug, device, and procedural ...

Actalent

Clinical Research Coordinator

Chapel Hill, NC · On-site

$22.25 - $29.50/hr

This role focuses on participant recruitment and consent, data collection and management, and ... Background in the medical field, including familiarity with phlebotomy. * Experience with chart ...

AA2IT

Medical Device Vigilance professionals

Raleigh, NC · Hybrid

$40 - $42/hr

Medical Device Vigilance Professionals Location: Raleigh, NC Pay Rate: $40-42/HR on W2 Full time - ... clinical safety and vigilance. * Strong organizational and project management skills. * Strong ...

AA2IT

Medical Device Vigilance professionals

Raleigh, NC · Hybrid

$40 - $42/hr

Medical Device Vigilance Professionals Location: Raleigh, NC Pay Rate: $40-42/HR on W2 Full time - ... clinical safety and vigilance. * Strong organizational and project management skills. * Strong ...

Duke University

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

Ranked sixth among medical schools in the nation, the School takes pride in being an inclusive ... Manage participant reimbursement and study-related communications. * Implement strategies to ...

Duke University

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

Ranked sixth among medical schools in the nation, the School takes pride in being an inclusive ... Manage participant reimbursement and study-related communications. * Implement strategies to ...

UNC HEALTH

Director Clinical Research

Raleigh, NC · On-site

... manages change to support program growth, operational efficiency, and high quality research ... Works collaboratively with medical staff and departmental representatives to determine study ...

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Medical Device Clinical Research Manager information

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$47.6K

$104.3K

$183.7K

How much do medical device clinical research manager jobs pay per year?

As of Sep 5, 2026, the average yearly pay for medical device clinical research manager in Raleigh, NC is $104,339.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,700.00 and $119,100.00 per year, depending on experience, location, and employer.

What does a medical device clinical research manager do?

A Medical Device Clinical Research Manager oversees the planning, execution, and management of clinical trials for new medical devices to ensure they meet regulatory and safety standards. They coordinate between research teams, regulatory bodies, and sponsors to ensure studies are conducted according to protocols and timelines. Their responsibilities include developing study protocols, managing budgets, ensuring data integrity, and ensuring compliance with regulatory requirements. This role is critical for bringing safe and effective medical devices to market.

What are the key skills and qualifications needed to thrive as a medical device clinical research manager?

To thrive as a Medical Device Clinical Research Manager, you need a solid background in life sciences or engineering, experience with clinical trial management, and a thorough understanding of regulatory requirements such as FDA and ISO standards. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like ACRP or SOCRA are highly beneficial. Exceptional leadership, problem-solving, and communication skills are crucial for coordinating cross-functional teams and managing complex projects. These skills ensure compliant, efficient, and successful clinical trials that bring safe and effective medical devices to market.

What are some of the common challenges faced by medical device clinical research managers when overseeing clinical trials?

Medical Device Clinical Research Managers often encounter challenges such as ensuring compliance with complex regulatory requirements, managing timelines across multiple sites, and coordinating with diverse stakeholders including investigators, sponsors, and regulatory bodies. They must also address issues related to patient recruitment and data integrity while maintaining clear communication within cross-functional teams. Strong organizational skills and adaptability are essential to navigate these challenges and deliver successful clinical trial outcomes.

What are the most commonly searched types of Medical Device Clinical Research jobs in Raleigh, NC?

The most popular types of Medical Device Clinical Research jobs in Raleigh, NC are:

What are popular job titles related to Medical Device Clinical Research Manager jobs in Raleigh, NC?

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

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The top searched job categories for Medical Device Clinical Research Manager jobs in Raleigh, NC are:

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Cities near Raleigh, NC with the most Medical Device Clinical Research Manager job openings:

Medical Device Clinical Research Manager jobs near you

Sr Clinical Research Associate

Veranex

Raleigh, NC • On-site

$98K - $140K/yr

Other

Re-posted 24 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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