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How much do clinical research study coordinator jobs pay per hour?

As of Aug 2, 2026, the average hourly pay for clinical research study coordinator in the United States is $28.69, according to ZipRecruiter salary data. Most workers in this role earn between $23.32 and $31.01 per hour, depending on experience, location, and employer.

What are Clinical Research Study Coordinators?

Clinical Research Study Coordinators are professionals responsible for managing the daily operations of clinical research studies. They ensure that studies are conducted according to protocol, regulatory requirements, and ethical standards. Their duties typically include recruiting and screening participants, collecting and managing data, coordinating with research teams, and maintaining study documentation. They play a crucial role in ensuring the quality and integrity of clinical trials, often acting as the primary point of contact between participants, investigators, and sponsors.

What is the difference between Clinical Research Study Coordinator vs Clinical Research Associate?

AspectClinical Research Study CoordinatorClinical Research Associate
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are commonOften requires a bachelor's or master's degree; certifications like CRA or CCRP are preferred
Work EnvironmentConducts site visits, manages study activities at clinical sitesMonitors multiple sites remotely or on-site, ensuring protocol compliance
Employer & Industry UsageEmployed by hospitals, research centers, or pharmaceutical companiesPrimarily employed by CROs or pharmaceutical companies for monitoring trials

While both roles support clinical trials, Study Coordinators manage day-to-day site activities, whereas Clinical Research Associates focus on monitoring and ensuring protocol adherence across multiple sites.

What are the key skills and qualifications needed to thrive as a Clinical Research Study Coordinator, and why are they important?

To thrive as a Clinical Research Study Coordinator, you need a strong understanding of clinical trial protocols, regulatory compliance (such as GCP), and typically a background in life sciences or healthcare. Familiarity with electronic data capture (EDC) systems, IRB submission processes, and certifications like ACRP or SOCRA are commonly required. Excellent organizational skills, attention to detail, and effective communication are crucial soft skills for managing study logistics and collaborating with multidisciplinary teams. These competencies ensure regulatory adherence, data integrity, and smooth study operations, which are vital to the success and credibility of clinical research.

What are some common challenges faced by Clinical Research Study Coordinators, and how can they be managed?

Clinical Research Study Coordinators often face challenges such as balancing multiple studies simultaneously, ensuring compliance with complex regulatory requirements, and maintaining clear communication between investigators, sponsors, and participants. Effective time management and strong organizational skills are crucial for staying on top of documentation, enrollment targets, and protocol adherence. Building collaborative relationships within the research team and staying up-to-date with regulatory changes can help coordinators overcome these challenges and contribute to the successful conduct of clinical trials.
More about Clinical Research Study Coordinator jobs
What cities are hiring for Clinical Research Study Coordinator jobs? Cities with the most Clinical Research Study Coordinator job openings:
What are the most commonly searched types of Clinical Research Study jobs? The most popular types of Clinical Research Study jobs are:
What states have the most Clinical Research Study Coordinator jobs? States with the most job openings for Clinical Research Study Coordinator jobs include:
What job categories do people searching Clinical Research Study Coordinator jobs look for? The top searched job categories for Clinical Research Study Coordinator jobs are:
Clinical Research Study Coordinator jobs near you
Infographic showing various Clinical Research Study Coordinator job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $59,666 per year, or $28.7 per hour.

Clinical Research Study Coordinator

Procom Services

Chapel Hill, NC

$20.75 - $27.50/hr

Contractor

Re-posted 28 days ago

Job description

Company Description

Procom is a leading provider of professional IT services and staffing to businesses and governments in Canada as well as the US.
With revenues over $500 million, the Branham Group has recognized Procom as the 3rd largest professional services firm in Canada and is now the largest "Canadian-Owned" IT staffing/consulting company.
Specialties Contract Staffing (Staff Augmentation)
Permanent Placement (Staff Augmentation)
ICAP (Contractor Payroll)
Flextrack (Vendor Management System)

Job Description

Clinical Research Study Coordinator

On behalf of our client, Procom Services is searching for a Clinical Research Study Coordinator to join their team in Chapel Hill, NC. The primary purpose of this position will be to run all aspects of the assigned clinical trials. IRB submissions, recruitment, working with investigators as well as the patients.


Clinical Research Study Coordinator Job Description

Perform independent and dependable work in preparation and coordination of study submission to IRB and other appropriate committees following regular deadlines.

They will provide draft IRB, Sponsor and other response to the PI for approval.

They will respond on behalf of the PI when appropriate

Communicate with study staff, IRB, sponsors, domestic and international study partners in a courteous and professional manner; Meet with study sponsor representatives as needed.

Attend IRB, study sponsor, or any other meeting in place of the PI

Prepare informed consent forms that follow appropriate regulation and meet sponsor requirements

Address queries and memos from IRB and other committees create draft response to query's for PI approval

Maintain and organize electronic and paper regulatory documents, study files and patient binders.

Perform Quality Assurance/Quality Control of Study files

Track and enter regulatory submissions using electronic databases and prepare reports within the databases.  

Respond to all queries and adverse events in a timely manner.

Will be initial contact for all adverse events for their studies

See clinical trial patients, follow up with phone calls and make sure all protocols are followed. Will also be responsible for screening and recruitment of clinical trial patients

Communicate for themselves and on behalf of the PI potential issues to regulatory supervisor, study team members, and investigators

Assist other staff members in completion of work in a team oriented fashion

Complete other regulatory duties as assigned.

Communication, Teamwork and Compliance

Employee uses effective verbal and written communication to accomplish tasks

Coordinator must have the technical ability to apply the knowledge of research principles when collecting, editing, analyzing the data and reporting data/information related to the study. 

The Coordinator will be required to have general computer and technical knowledge as well as an understanding of patient input data bases. 

Requires ability to identify discrepancies in database information.

Coordinator must be able to problem solve and implant new systems to help make Center more effective. This type of work requires extreme organization and attention to detail.

Coordinator will support research, develop programs and policies for the Center.

Coordinator must be able to work as a productive member of a team by helping develop solutions to meet group needs as well as the structure of the team. 

Coordinator will have the ability to serve as a team leader.

Skills include working effectively with patients, medical faculty and staff, ability to understand and implement protocols and teach them to clinic personnel. 

Requires ability to develop a flexible work schedule, organized and able to implement clinic clinical trials based on FDA and good clinical practice guidelines and work independently.

Experience in research is required. 

Knowledge of research principles and methods to interpret, and coordinate the collection and analysis of data/information related to the research.

Clinical Research Study Coordinator Mandatory Requirements

Prior experience in Clinical Trials.

Nursing degree preferred, specifically with a focus in Oncology.


Clinical Research Study Coordinator Start Date

ASAP


Clinical Research Study Coordinator Assignment Length

6 months (possible extension/hire)

Additional Information
PLEASE NOTE THAT WE ARE NOT ABLE TO WORK WITH CANDIDATES ON H1B VISAS OR CANDIDATES REPRESENTED BY THIRD PARTIES.

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