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Associate Biomedical Engineering Technologist Jobs in Raleigh, NC

... biomedical engineering, or a health-related field of study. Experience requirements: 3 years of ... Serving as a Lead Clinical Research Associate (CRA) for clinical studies; Clinical Trial Management ...

... biomedical engineering, or a health-related field of study. Experience requirements: 3 years of ... Serving as a Lead Clinical Research Associate (CRA) for clinical studies; Clinical Trial Management ...

... biomedical engineering, or a health-related field of study. Experience requirements: 3 years of ... Serving as a Lead Clinical Research Associate (CRA) for clinical studies; Clinical Trial Management ...

Senior Electrical Engineer R&D

Morrisville, NC · On-site

$100K - $131K/yr

We are a growing team of technology developers seeking candidates interested in helping advance our ... B.S. in Electrical Engineering, Biomedical Engineering, or a related field. * 5+ years of ...

Senior Electrical Engineer R&D

Morrisville, NC · On-site

$100K - $131K/yr

We are a growing team of technology developers seeking candidates interested in helping advance our ... B.S. in Electrical Engineering, Biomedical Engineering, or a related field. * 5+ years of ...

Senior Electrical Engineer R&D

Morrisville, NC · On-site

$100K - $131K/yr

We are a growing team of technology developers seeking candidates interested in helping advance our ... B.S. in Electrical Engineering, Biomedical Engineering, or a related field. * 5+ years of ...

Stay current with emerging technologies and best practices in machine learning, software ... D. in Biomedical Engineering, Computer Science, Electrical Engineering, Medical Physics, Imaging ...

Stay current with emerging technologies and best practices in machine learning, software ... D. in Biomedical Engineering, Computer Science, Electrical Engineering, Medical Physics, Imaging ...

... technologies. The candidate should be able to plan and conduct scientific experiments, and ... Textile engineering, Biomedical Engineering, Materials Science and Engineering, or related ...

The Post Doctoral Associate will apply their technical skills toward the development ... biomedical engineering, biomedical informatics, biostatistics or a related discipline. Required ...

Showing results 41-60

Associate Biomedical Engineering Technologist information

See Raleigh, NC salary details

$39.9K

$92.2K

$136.1K

How much do associate biomedical engineering technologist jobs pay per year?

As of Aug 23, 2026, the average yearly pay for associate biomedical engineering technologist in Raleigh, NC is $92,160.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,400.00 and $112,800.00 per year, depending on experience, location, and employer.

What is the difference between Associate Biomedical Engineering Technologist vs Biomedical Engineering Technologist?

AspectAssociate Biomedical Engineering TechnologistBiomedical Engineering Technologist
CredentialsDiploma or associate degree, certification often preferredBachelor's degree in biomedical engineering or related field
Work EnvironmentHospitals, clinics, medical device companiesResearch labs, hospitals, medical device manufacturing
Employer & Industry UsageEntry-level support roles in healthcare and medical device sectorsTechnical roles requiring more advanced knowledge and responsibilities

The main difference between an Associate Biomedical Engineering Technologist and a Biomedical Engineering Technologist lies in their education and experience level. The associate role typically requires a diploma or associate degree and involves entry-level support tasks, while the technologist role requires a bachelor's degree and involves more complex technical responsibilities. Both roles are vital in healthcare settings, but the technologist generally has a broader scope of work and higher qualifications.

What can I do with an associate biomedical engineering technologist?

An associate biomedical engineering technologist can work in healthcare facilities, assisting with the maintenance, calibration, and repair of medical equipment. They often collaborate with biomedical engineers and may need to be familiar with medical device software and safety standards. This role typically involves technical troubleshooting and ensuring equipment compliance with healthcare regulations.

What does an Associate Biomedical Engineering Technologist do?

An Associate Biomedical Engineering Technologist assists in maintaining, repairing, and calibrating medical equipment used in healthcare settings. They perform routine inspections, troubleshoot technical issues, and ensure devices meet safety and performance standards, often working under the supervision of senior technologists or engineers. Familiarity with medical device software and safety protocols is essential in this role.

What are the most commonly searched types of Biomedical Engineering Technologist jobs in Raleigh, NC?

The most popular types of Biomedical Engineering Technologist jobs in Raleigh, NC are:

Infographic showing various Associate Biomedical Engineering Technologist job openings in Raleigh, NC as of August 2026, with employment types broken down into 11% Internship, 67% Full Time, 11% Part Time, and 11% Contract. Highlights an 89% In-person, and 11% Remote job distribution, with an average salary of $92,160 per year, or $44.3 per hour.

Senior Clinical Research Associate

Parexel

Raleigh, NC • On-site

Full-time

Posted 13 days ago


Parexel rating

8.2

Company rating: 8.2 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

30th of 74 rated research


Job description

Name of Employer: Parexel International LLC
Position Title: Sr. Clinical Research Associate
*Multiple Openings Available*
Position Location: 541 Church at North Hills St., Suite 1000, Raleigh, NC 27609
*100% Remote reporting to Raleigh, NC.
Hours: Full Time / 40 hours per week
Summary of Duties: Engaged in monitoring clinical research that involves understanding human diseases and improving human health. Monitor and oversee clinical trials at client sites. Evaluate quality and integrity of reported data. Represent the company at assigned clinical trial sites and be accountable for quality and delivery from site identification to the close of trial. Conduct, drive, and manage country-specific feasibility and site pre-qualification and qualification activities, which include preparation, negotiation, and facilitation of execution of Confidentiality Agreements (CDA), Clinical Site Agreements (CSAs), and any amendments. Conduct on-site and remote visits/contacts, including Qualification, Initiation, Monitoring, Termination Visits, and Site Motivational Visits, and generate site visit reports. Develop strategy to configure, distribute, and collect, review, and approve high-quality country-specific and site-specific documents, essential regulatory documents, and updated or amended regulatory documentation. Customize, review, and negotiate country/site-specific Informed Consent Forms, translations, and customize and negotiate any amendments. Prepare and submit IRB/IEC and MoH/RA applications, resolve conflicts, and determine appropriate follow-up until receipt of final approval. Address and resolve issues at clinical trial sites, including the need for additional training, potential deficiencies in documentation, and communication. Follow-up on Case Report Form data entry, query status, and Serious Adverse Events. Assess and manage test article/study supply including supply, accountability, and destruction/return status. Review and follow-up on site payment status and ensure site receives payments on a timely manner. Communicate study issues that require immediate action with a proposed strategy for resolution. Ensure assigned sites are audit-ready and inspection-ready. Lead and mentor junior CRAs on process/study requirements and perform assessments and co-monitoring visits. Perform report review of visit reports of junior CRAs to ensure compliance with GCP and Protocol Guidelines. Guide Administrative Support Team members, review work, and provide feedback to the manager regarding performance.
Education requirements: Bachelor's degree or equivalent in biological science, pharmaceutical sciences, chemistry, biotechnology, biomedical engineering, or a health-related field of study.
Experience requirements: 3 years of experience in clinical research.
Or, alternatively:
Education requirements : Master's degree or equivalent in biological science, pharmaceutical sciences, chemistry, biotechnology, biomedical engineering, or a health-related field of study.
Experience requirements: 1 year of experience in clinical research.
Special Skills or Other Requirements: Applicants must have demonstrated experience with:
Serving as a Lead Clinical Research Associate (CRA) for clinical studies; Clinical Trial Management System (CTMS) and Electronic Document Management System (EDMS); Site Management and application of clinical trial methodology and terminology; Independently monitoring visits (Qualification, Site Initiation, and Monitoring); Working with clinical research, phases of clinical trials, current GCP/ICH, and country clinical research law and guidelines; and Communicating results to stakeholders in non-technical language.
Travel requirements: Up to 75% Domestic Travel.
*Position eligible for Employee Referral Program*
To apply: Individuals interested in applying for the position may email a resume with Job #ES2401 to openings@parexel.com

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About PAREXEL

Sourced by ZipRecruiter

Bring your Data Management expertise to Parexel's Strategic Partnerships. Although we work globally, each partnership we form is deeply personal. We are as dedicated to every aspect of our client's product development as they are - and work closely with client teams in true partnership to understand both challenges and opportunities. At Parexel we are focused on meeting customer and patient needs through collaborative partnership so that we get treatments into the hands of patients who need them most.

Industry

Pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Waltham, MA, US

Year founded

1983