ZipRecruiter

Log In

1

Clinical Research Studies Jobs (NOW HIRING)

Stryde Research

Clinical Research Coordinator

Plano, TX · On-site

$50K - $80K/yr

The Clinical Research Coordinator will oversee and manage clinical research studies, ensuring compliance with protocols and regulations. Responsibilities include obtaining informed consent from ...

previous pagenext page

Showing results 21-40

All JobsClinical Research Studies Jobs

Clinical Research Studies information

See salary details

$49K

$107.3K

$189K

How much do clinical research studies jobs pay per year?

As of Aug 8, 2026, the average yearly pay for clinical research studies in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What is the difference between Clinical Research Studies vs Clinical Research Coordinators?

AspectClinical Research StudiesClinical Research Coordinators
CredentialsOften require degrees in health sciences, certifications like CCRPRequire similar degrees, certifications like CCRP or CRC preferred
Work EnvironmentInvolves designing, planning, and overseeing studiesFocuses on managing daily study activities, patient interactions
Employer & IndustryPharmaceutical companies, research institutions, CROsHospitals, clinics, research sites
Search & Comparison IntentUnderstanding roles in clinical research processJob responsibilities and qualifications of coordinators

Clinical Research Studies involve designing and overseeing research protocols, while Clinical Research Coordinators handle daily study operations and patient interactions. Both roles require relevant certifications and work within the clinical research industry, but they differ in scope and responsibilities.

More about Clinical Research Studies jobs
What cities are hiring for Clinical Research Studies jobs? Cities with the most Clinical Research Studies job openings:
What states have the most Clinical Research Studies jobs? States with the most job openings for Clinical Research Studies jobs include:
What job categories do people searching Clinical Research Studies jobs look for? The top searched job categories for Clinical Research Studies jobs are:
Clinical Research Studies jobs near you
Infographic showing various Clinical Research Studies job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Coordinator Clinical Research

McLaren Health Care Corp

Flint, MI

$23.50 - $31.25/hr

Full-time

Re-posted 20 days ago

McLaren Health Care rating

6.7

Company rating: 6.7 out of 10

Based on 221 frontline employees who took The Breakroom Quiz

533rd of 887 rated healthcare providers

Job description

Position Summary:

Responsible for facilitating research studies; providing knowledgeable information regarding each research protocol to the medical and nursing staff; evaluating the eligibility of potential candidates for research studies; assisting in the informed consent process; monitoring research study compliance; collecting and submitting data; coordinating required study procedures to meet protocol requirements and maintain a system for effective data flow. 

Essential Functions and Responsibilities:

1.      Evaluates eligibility of candidates for clinical research studies by reviewing protocol defined eligibility requirements and/or collecting pertinent data on potential candidates, verifying appropriateness of patients for entry to clinical trials, and assisting the other staff in determining eligibility of potential patients.

2.      Assists the investigator with the informed consent process and assures that the research team and the patient have adequate information to achieve the informed consent process.

3.      Registers and randomizes eligible patients.

4.      Submits accurately completed data collection forms to the sponsor or CRO in a timely manner as dictated by the study protocol.

5.      Coordinates tests and procedures as specified in the study protocol through accurate communication with the site / principal investigator, physicians, patients, nurses, and office/hospital staff.

6.      Maintains contact with regulatory specialist to ensure data submitted to the IRB of record is accurate and timely. Upon request, submits regulatory documents to regulatory specialist to include in the IRB submission or submission to sponsor or CRO.

7.      Assists the investigators and clinicians in identifying and enrolling eligible patients into clinical trials/ studies and assures compliance to protocol requirements.

8.      Educates patients and their families regarding research protocols and keeps them informed of procedures and changes in the studies in which they are participating.

Qualifications:

Required:

  • High School Diploma or equivalent
  • Two years' experience in clinical research or five-years in a health care role (ex. paramedic, emergency medical technician, radiology technician) 

Preferred: 

  • Degree in biology, psychology, or other clinical research -related area or equivalent education and experience
  • Three or more years of experience in clinical research
  • Clinical research certification through SOCRA or ACRP

Equal Opportunity Employer of Minorities/Females/Disabled/Veterans

Additional Information
  • Schedule: Full-time
  • Requisition ID: 26002728
  • Daily Work Times: 8am - 4:30pm
  • Hours Per Pay Period: 80
  • On Call: No
  • Weekends: No

What McLaren Health Care employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply