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Diabetes Research Assistant Jobs in Raleigh, NC (NOW HIRING)

The research assistant is primarily responsible for assisting in research patient visits according ... Perform trial frame refraction and Early Treatment Diabetic Retinopathy Study (ETDRS) visual acuity ...

Physician Assistant

Morrisville, NC ยท On-site

$95 - $120/hr

Provide patient and/or family education regarding diabetes, nutrition, smoking cessation, pain ... Participate in clinic research activities if needed * Perform telehealth visits if needed * Work ...

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Diabetes Research Assistant information

See Raleigh, NC salary details

$9

$25

$52

How much do diabetes research assistant jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for diabetes research assistant in Raleigh, NC is $25.30, according to ZipRecruiter salary data. Most workers in this role earn between $16.26 and $29.51 per hour, depending on experience, location, and employer.

What is a diabetes research assistant?

A Diabetes Research Assistant supports research studies focused on diabetes by collecting and analyzing data, assisting in laboratory experiments, and coordinating clinical trials. They work under the supervision of lead researchers or principal investigators to ensure accuracy and compliance with study protocols. Their role may also involve recruiting participants, maintaining records, and preparing reports for publication. This position is critical in advancing diabetes treatments and improving patient outcomes.

What are the typical daily responsibilities of a diabetes research assistant?

As a Diabetes Research Assistant, your daily activities may include collecting and processing biological samples, assisting with patient recruitment and consent, maintaining accurate research records, and managing study data. You might also help administer patient tests, monitor adherence to research protocols, and coordinate with multidisciplinary teams, including physicians, nurses, and other researchers. Tasks can vary based on the stage of the study, but attention to detail and consistent documentation are always key. Regular communication with both study participants and team members is essential to smooth project progression and participant care.

What are the key skills and qualifications needed to thrive as a diabetes research assistant?

A Diabetes Research Assistant typically needs a background in life sciences or health-related fields, with experience in laboratory techniques and clinical research methodologies. Familiarity with data collection tools, statistical analysis software (such as SPSS or SAS), and compliance with regulations like HIPAA and Good Clinical Practice is often expected. Excellent attention to detail, organization, and strong verbal and written communication skills help ensure high-quality results and teamwork. Mastering both technical and interpersonal competencies is crucial for supporting successful research studies and ensuring data integrity.

What are the most commonly searched types of Diabetes Research jobs in Raleigh, NC?

The most popular types of Diabetes Research jobs in Raleigh, NC are:

What are popular job titles related to Diabetes Research Assistant jobs in Raleigh, NC?

For Diabetes Research Assistant jobs in Raleigh, NC, the most frequently searched job titles are:

What cities near Raleigh, NC are hiring for Diabetes Research Assistant jobs?

Cities near Raleigh, NC with the most Diabetes Research Assistant job openings:

Infographic showing various Diabetes Research Assistant job openings in Raleigh, NC as of July 2026, with employment types broken down into 92% Full Time, and 8% Part Time. Highlights an 93% In-person, and 7% Remote job distribution, with an average salary of $52,615 per year, or $25.3 per hour.

Clinical Research Assistant

Wake Forest, NC โ€ข On-site

North Carolina Retina Associates
11 - 50 employees

$25 - $30/hr

Full-time

Posted 5 days ago


Job description

NC Retina Associates is looking for a Research Assistant to join our team! The research assistant is primarily responsible for assisting in research patient visits according to International Council for Harmonisation Good Clinical Practice (ICH-GCP) guidelines and according to the Institutional Review Board (IRB)-approved study protocol and/or manual of procedures. Day-to-day activities may include all or some of the essential functions listed below, depending upon individual experience / knowledge and the needs of the organization which are subject to change from time to time.

Duties:
  • Coordinate and schedule subject visits within study/subject specific windows per protocol guidelines.
  • Prepare visit-specific documentation and charts for Clinical Research Coordinator.
  • Observe Coordinator in patient care and management.
  • Assist Coordinator in monitoring subject flow and assist in subject care and management.
  • Observe, assist, collect and record all necessary data for follow up (e.g. adverse events, concomitant medications, etc.) study visits (Phase 2 & 3; NO Gene Therapy).
  • Transcribe subject study information from source documents to the Electronic Case Report Forms.
  • Administer all mandatory questionnaires to study subjects.
  • Set up, prepare subject, and conduct electrocardiograms (ECG) on subjects as required per study protocol.
  • Promptly request all necessary medical records for Serious Adverse Event Reporting.
  • Process and ship laboratory biological samples for analysis.
  • Perform intraocular pressure checks after injections.
  • Perform trial frame refraction and Early Treatment Diabetic Retinopathy Study (ETDRS) visual acuity testing (For Investigator Sponsored Trials (IST)s only, at selected sites).
  • Inform subjects and obtain written re-consents in regard to Informed Consent Form (ICF)’s (selected studies)
  • Observe and assist scribe in ocular exams for doctors and confirm appropriate treatment per protocol.
  • Perform other duties as assigned.
  • Obtain any applicable additional/required sponsor training and/or certifications.

Minimum Qualifications:
  • High School diploma or the equivalent, with significant relevant experience.
  • College degree preferred.
  • Ophthalmic experience preferred.
  • Effective oral and written communication.
  • Delivers safe and appropriate care to patients in addition to the requirements outlined by study protocols.