1

Clinical Research Studies Jobs (NOW HIRING)

Be Seen First

Clinical Research Coordinator / Study Coordinator We are seeking a motivated and organized Clinical Research Coordinator (CRC) / Study Coordinator to join our growing clinical research team. The CRC ...

New

Be Seen First

Recruits patients for clinical research studies based on study inclusion/exclusion. * Obtains informed consent from subject and conducts the screening visit. * Completes paperwork related to subject ...

Be Seen First

Clinical Research Coordinator / Study Coordinator We are seeking a motivated and organized Clinical Research Coordinator (CRC) / Study Coordinator to join our growing clinical research team. The CRC ...

New

Be Seen First

Clinical Research Coordinator / Study Coordinator We are seeking a motivated and organized Clinical Research Coordinator (CRC) / Study Coordinator to join our growing clinical research team. The CRC ...

New

Coordinator Clinical Research

Flint, MI · On-site

$23.50 - $31.25/hr

Responsible for facilitating research studies; providing knowledgeable information regarding each research protocol to the medical and nursing staff; evaluating the eligibility of potential ...

next page

Showing results 1-20

Clinical Research Studies information

See salary details

$49K

$107.3K

$189K

How much do clinical research studies jobs pay per year?

As of Aug 13, 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:

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, 72% Full Time, 17% 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.

Clinical Research Coordinator

KAD Clinical Research

Affton, MO • On-site

$25 - $45/hr

Part-time

This job post has expired 1 day ago. Applications are no longer accepted.


Job description

Clinical Research Coordinator / Study Coordinator

We are seeking a motivated and organized Clinical Research Coordinator (CRC) / Study Coordinator to join our growing clinical research team. The CRC will be responsible for coordinating day-to-day clinical trial activities while working closely with investigators, patients, sponsors, CROs, and other members of the research team.

Key Responsibilities:

  • Coordinate clinical research studies from study start-up through completion
  • Recruit, pre-screen, screen, and schedule potential study participants
  • Conduct study visits according to study protocols
  • Obtain and maintain accurate source documentation and study records
  • Complete data entry and respond to sponsor/CRO queries in a timely manner
  • Coordinate laboratory samples, study supplies, investigational product, and study-related procedures
  • Communicate with sponsors, CROs, monitors, investigators, and research staff
  • Assist with monitoring visits, site initiation visits, and study closeout activities
  • Maintain strong organization and ensure studies are conducted according to protocol, GCP, and applicable requirements
  • Provide a positive, professional experience for study participants throughout their participation

Qualifications:
Previous clinical research or healthcare experience is preferred. The ideal candidate is highly organized, dependable, detail-oriented, comfortable working directly with patients, and able to manage multiple studies and priorities in a fast-paced environment.

Clinical Research Coordinator experience, phlebotomy experience, and knowledge of GCP are preferred but may not be required for the right candidate.