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Medical Research Study Jobs (NOW HIRING)

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Medical Research Associate

Lenexa, KS · On-site

Medical Research Associate - Lenexa, KS (Onsite) ICON is a global healthcare intelligence and ... Your role will extend beyond the clinical aspects as you chaperone study subjects during their ...

ICON

Senior Medical Research Associate

Lenexa, KS · On-site

We are seeking a (PRN) Senior Medical Research Associate with active Paramedic licensure to support clinical research studies at our Lenexa, Kansas (KS) clinic. Whether you're exploring a career in ...

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Medical Research Study information

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$37.5K

$53.3K

$58.5K

How much do medical research study jobs pay per year?

As of Jun 10, 2026, the average yearly pay for medical research study in the United States is $53,326.00, according to ZipRecruiter salary data. Most workers in this role earn between $54,000.00 and $58,000.00 per year, depending on experience, location, and employer.
Infographic showing various Medical Research Study job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 91% Full Time, 5% Part Time, 2% Temporary, and 1% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $53,326 per year, or $25.6 per hour.

Assistant Research Study Coordinator

Georgia Clinical Research LLC

Lawrenceville, GA • On-site

$19 - $24/hr

Full-time

Retirement

Posted 29 days ago

Job description

Assist the Study Coordinators (SC) by collecting and recording data per protocol requirements in accordance with the Sponsor Protocol, CFR section 21, and standard Good Clinical practices. This position interfaces between the Subject, the Sponsor pharmaceutical company, various pharmaceutical company vendors, and laboratories. The Assistant Study Coordinator will collect, record, file, and review data in accordance with the criteria listed in the Sponsor protocol.

Responsible for providing accurate documentation in compliance with good clinical practice (GCP) and in accordance with ICH and the FDA Code of Federal Regulations

The Assistant Study Coordinator is one of the contacts and/or liaisons between the Sponsor Monitor and the site. She/he will ensure the accuracy of data and assist with the operational success of the study. He or she ensures timely and accurate collection of data, entries into RDC, IVRS, and query resolution. S/he/he is often training to become a full-time Study Coordinator.

Other tasks may be required of the Assistant Study coordinator to assist management with proper billing for study services and subject procedures.

Company Description

Independent Research facility located within Regan Medical Center.