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

With a focus on providing talent for field/inside sales, medical device support, clinical support, and medical affairs our TESO division has 10,000+ field professionals in more than 30 countries ...

MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on ... We support the pharmaceutical, biotech, and medical device industries with our proven, scientific ...

Expertise in medical device sales and clinical workflows. * Proficiency in CRM systems (e.g., Salesforce) and Microsoft Office Suite. * Strong organizational and time-management skills. * Ability to ...

Clinical Applications Specialist I

Morrisville, NC · Hybrid

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Position Summary The Clinical Applications Specialist I (CAS I) provides product applications and ... Medical device industry experience a plus. Knowledge, Skills, and Abilities * Consistently upholds ...

Clinical Applications Specialist I

Morrisville, NC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Position Summary The Clinical Applications Specialist I (CAS I) provides product applications and ... Medical device industry experience a plus. Knowledge, Skills, and Abilities * Consistently upholds ...

Clinical Applications Specialist I

Morrisville, NC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Position Summary The Clinical Applications Specialist I (CAS I) provides product applications and ... Medical device industry experience a plus. Knowledge, Skills, and Abilities * Consistently upholds ...

Showing results 41-60

Medical Device Clinical information

See Raleigh, NC salary details

$96.7K

$109.4K

$120.5K

How much do medical device clinical jobs pay per year?

As of Aug 19, 2026, the average yearly pay for medical device clinical in Raleigh, NC is $109,359.00, according to ZipRecruiter salary data. Most workers in this role earn between $103,000.00 and $115,700.00 per year, depending on experience, location, and employer.

What is a medical device clinical professional?

Medical Device Clinical professionals are specialists who oversee and manage the clinical aspects of medical device development and testing. They are responsible for planning, executing, and monitoring clinical trials to ensure medical devices are safe and effective for patient use. Their work involves collaborating with regulatory bodies, healthcare providers, and research organizations to collect and analyze clinical data. These professionals play a key role in ensuring that medical devices comply with regulatory requirements before they reach the market.

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

To thrive as a Medical Device Clinical Specialist, you need a solid background in life sciences or nursing, strong clinical knowledge, and often a relevant degree or certification. Familiarity with medical device technologies, regulatory standards, and clinical trial management systems is typically required. Excellent communication, problem-solving, and relationship-building skills help you effectively train healthcare professionals and support product adoption. These skills are crucial for ensuring safe, effective device use and successful integration into clinical environments.

What are some common challenges faced by professionals in medical device clinical roles, and how can they be addressed?

Professionals in Medical Device Clinical roles often encounter challenges such as navigating complex regulatory requirements, coordinating multi-site clinical trials, and ensuring timely patient recruitment. To address these, strong organizational skills, clear communication with cross-functional teams, and ongoing education about evolving regulations are essential. Building strong relationships with investigators and site staff can also help streamline trial processes and ensure high-quality data collection.

What is the difference between Medical Device Clinical vs Medical Device Quality Assurance?

AspectMedical Device ClinicalMedical Device Quality Assurance
CertificationsClinical Research Certification, GCP trainingISO 13485, GMP training
Work EnvironmentHospitals, clinics, clinical research settingsManufacturing facilities, quality labs
Employer & Industry UsageMedical device companies, research organizationsManufacturers, regulatory agencies
Primary FocusClinical trials, patient safety, device efficacyProduct quality, compliance, process validation

Medical Device Clinical roles focus on conducting clinical trials and ensuring device safety and efficacy, often working directly with patients. In contrast, Medical Device Quality Assurance emphasizes maintaining product quality, regulatory compliance, and manufacturing standards. Both roles are essential in the medical device industry but serve different functions within the product lifecycle.

What does a medical device clinical specialist do?

A medical device clinical specialist is responsible for training healthcare professionals on the proper use of medical devices, providing technical support, and ensuring compliance with regulatory standards. They often work closely with sales teams, conduct product demonstrations, and gather user feedback to improve device performance and safety.

What cities near Raleigh, NC are hiring for Medical Device Clinical jobs?

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

Infographic showing various Medical Device Clinical 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 $109,359 per year, or $52.6 per hour.

Engineer 1, Design Development, R&D

Teleflex

Morrisville, NC • On-site

Full-time

Posted 21 days ago


Teleflex rating

8.3

Company rating: 8.3 out of 10

Based on 27 frontline employees who took The Breakroom Quiz


Job description

Expected Travel: Up to 10%
Requisition ID: 14175
About Teleflex Incorporated
As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people's lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare.
Teleflex is the home of Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ - trusted brands united by a common sense of purpose.
At Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com.
Vascular & Emergency Medicine - Built on a legacy of innovation and clinical excellence, the Vascular & Emergency Medicine business at Teleflex develops and delivers advanced medical technologies that empower clinicians to help improve patient outcomes and optimize healthcare efficiency. Our trusted Arrow™, Arrow™, EZ-IO™, and QuikClot™ brands set the standard for vascular access and emergency medicine, offering proven solutions to enhance patient outcomes. From technically advanced vascular access devices - including central venous and arterial catheters, PICCs, and sheath introducers with antimicrobial protection-to life-saving intraosseous access systems and hemostatic technologies used by hospitals, EMS, and military teams worldwide, our portfolio embodies precision, reliability, and performance. As part of a high-performing, purpose-driven organization, we are united by a commitment to clinical differentiation, innovation, and excellence. Join a dynamic, growth-focused team that offers advanced medical technology solutions that make a lasting impact on healthcare.
Position Summary
This is an entry-level engineering position supporting the new product development engineering group for the Emergency Medicine product families. Assignments may also include work for other products within the Teleflex VEM portfolio. Medical device experience is preferred. Incumbent organizes and manages multiple projects and executes them in a timely manner. Assignments will focus on providing creative solutions to new products or existing product improvements as needs arise. Performs other duties as required or assigned.
DISTINGUISHING CHARACTERISTICS:
Incumbent at this level executes on the scope of assignments by planning, designing, and coordinating the development of engineering activities to support new product development and changes/ improvements to existing product lines. These projects can exist anywhere from the early concept stage through manufacturing transfer and scale-up. Incumbent at this level receives instruction and assistance as needed and is aware of the work unit's operating procedures and policies.
Principal Responsibilities
• Supports research and project initiatives by working with clinicians, researchers, and vendors which may involve travel to sites within the United States.
• Gathers data on current state of the art, practices, policies, etc. to support unmet needs development.
• Prepares protocols and coordinates execution for exploratory work, research, and prototyping for various medical devices and components.
• Assists with the development of Design History Files.
• Supports multiple projects and ensures they are completed in a timely manner.
• Applies mechanical design skills to the creation and/or modification of existing medical device designs, test fixturing and manufacturing equipment.
• Helps generate design ideas for new products as well as solutions to existing products when modifications are requested.
• Demonstrates professional responsibility by cooperating with other personnel to achieve departmental goals and objectives.
MARGINAL FUNCTIONS
• Enhances growth and development through participation in education programs, training meetings and workshops, and remaining apprised of current literature.
• Participates actively in continuous quality improvement activities through compliance with safety standards.
• Maintains compliance with principles of accepted employee conduct as identified in the Teleflex employee handbook and as specified in departmental policies and procedures.
• Performs other related duties as assigned or requested.
Education / Experience Requirements
• Possession of a bachelor's degree in engineering.
• One year of medical device or other related research experience minimum is preferred.
• Experience in using SolidWorks CAD (design/drafting) program.
• Proficient using Microsoft Office Suite (Project, Word, Excel, PowerPoint)
• Background with injection molding, plastic extrusion and plastic part assembly process and methods desired.
• Experience with U.S. FDA GMP and ISO requirements for design, risk management, and validation preferred.
• ISO and ASTM testing methods for medical devices preferred.
• An understanding of regulations pertaining to medical device design and design modifications preferred.
Specialized Skills / Other Requirements
Skill Sets:
• Strong written and verbal communication skills with attention to detail.
• Ability to effectively present information and respond to questions from managers, clients, and customers.
• Ability to solve practical problems and deal with a variety of variables in situations where only limited standardization exists.
• Ability to analyze complex technical information and adopt an effective course of action.
• Ability to create effective presentations and participate in a variety of meetings and conferences.
Ability To:
• Demonstrate creativity and ingenuity in applying engineering principles and practices.
• Draw solutions form a wider range of experience.
• Organize, evaluate, and coordinate engineering studies with a cross-functional team.
• Conduct comprehensive studies and preparation of reports.
• Speak and write English fluently.
#LI-DR1
At Teleflex, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front.
Teleflex Incorporated is an equal opportunity employer. Applicants will be considered without regard to age, race, religion, color, national origin, ancestry, sexual orientation, disability, nationality, sex, or veteran status. If you require accommodation to apply for a position, please contact us at: 877-880-8588 or Talent@Teleflex.com.
Teleflex, the Teleflex logo, Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries.
© 2026 Teleflex Incorporated. All rights reserved.

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