Study coordinator vs clinical trial coordinator

The differences between study coordinators and clinical trial coordinators can be seen in a few details. Each job has different responsibilities and duties. It typically takes 1-2 years to become both a study coordinator and a clinical trial coordinator. Additionally, a clinical trial coordinator has an average salary of $50,720, which is higher than the $47,435 average annual salary of a study coordinator.

The top three skills for a study coordinator include patients, informed consent and IRB. The most important skills for a clinical trial coordinator are clinical trials, patients, and informed consent.

Study coordinator vs clinical trial coordinator overview

	Study Coordinator	Clinical Trial Coordinator
Yearly salary	$47,435	$50,720
Hourly rate	$22.81	$24.38
Growth rate	6%	6%
Number of jobs	14,929	64,859
Job satisfaction	-	-
Most common degree	Bachelor's Degree, 61%	Bachelor's Degree, 62%
Average age	44	44
Years of experience	2	2

What does a study coordinator do?

Study coordinators oversee the entire process of clinical research from its inception to its completion. The coordinators make certain that human subjects are safe and well-protected. They identify the eligibility of the subject through clinical record screening and medical information extracting. It is their responsibility to maintain the regulatory documents based on the requirements of the Food and Drug Administration (FDA). They should develop skills and knowledge in clinical trials, study protocol, and patient care.

What does a clinical trial coordinator do?

A clinical trial coordinator is responsible for assisting in medical trials and clinical research studies. Clinical trial coordinators support the whole operational process of medical research from its conceptualization until the final outputs. They manage the adequacy of tools and equipment, ensuring the cleanliness and orderliness of the facilities to prevent potential hazards and delays in laboratory testing. A clinical trial coordinator must have excellent communication and organizational skills, especially in writing progress reports and securing the acquired laboratory samples.

Study coordinator vs clinical trial coordinator salary

Study coordinators and clinical trial coordinators have different pay scales, as shown below.

	Study Coordinator	Clinical Trial Coordinator
Average salary	$47,435	$50,720
Salary range	Between $34,000 And $65,000	Between $35,000 And $72,000
Highest paying City	Oakland, CA	Berkeley, CA
Highest paying state	Connecticut	California
Best paying company	Bloodworks Northwest	Mohawk Valley Health System
Best paying industry	Health Care	Health Care

Differences between study coordinator and clinical trial coordinator education

There are a few differences between a study coordinator and a clinical trial coordinator in terms of educational background:

	Study Coordinator	Clinical Trial Coordinator
Most common degree	Bachelor's Degree, 61%	Bachelor's Degree, 62%
Most common major	Nursing	Nursing
Most common college	University of Michigan - Ann Arbor	University of Pennsylvania

Study coordinator vs clinical trial coordinator demographics

Here are the differences between study coordinators' and clinical trial coordinators' demographics:

	Study Coordinator	Clinical Trial Coordinator
Average age	44	44
Gender ratio	Male, 23.7% Female, 76.3%	Male, 23.9% Female, 76.1%
Race ratio	Black or African American, 2.6% Unknown, 7.6% Hispanic or Latino, 15.5% Asian, 8.9% White, 64.8% American Indian and Alaska Native, 0.5%	Black or African American, 2.6% Unknown, 7.6% Hispanic or Latino, 15.2% Asian, 10.5% White, 63.6% American Indian and Alaska Native, 0.5%
LGBT Percentage	9%	9%

Differences between study coordinator and clinical trial coordinator duties and responsibilities

Study coordinator example responsibilities.

Manage and analyze EKG and sleep data collect from subjects in confidential database.
Establish and maintain strong community partnerships to achieve HIV prevention objectives.
Conduct consent discussions and other study procedures per protocol and CFR and GCP guidelines.
Maintain strict patient confidentiality according to HIPPA regulations, GCP and ICH , 21 CFR and other regulatory documentation.
Maintain accurate IRB, regulatory and study documentation to insure compliance with protocol and good clinical practice guidelines.
Coordinate day-to-day study activities including data collection and statistical analysis, protocol development/implementation, IRB relations, and staff development.

Clinical trial coordinator example responsibilities.

Establish and maintain strong community partnerships to achieve HIV prevention objectives.
Coordinate grant and IRB renewals and submissions; and preparation of publications, study protocols and manuals of operations.
Develop a GUI tool for volume & surface area of lesion/hematoma/edema in stroke MRI.
Privilege to negotiation principles from the consumers stand point within the divisions of: oncology, bariatric, cosmetic & cardiovascular.
Compose SPSS syntax to simplify data import process, reducing the time require from a full day to a few minutes.
Analyze collected data using SPSS to determine possible significant findings.

Study coordinator vs clinical trial coordinator skills

Common study coordinator skills

Patients, 14%
Informed Consent, 9%
IRB, 7%
Data Collection, 5%
FDA, 5%
Clinical Trials, 4%

Common clinical trial coordinator skills

Clinical Trials, 12%
Patients, 11%
Informed Consent, 10%
IRB, 4%
Meeting Minutes, 4%
FDA, 4%

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Study Coordinator
Study Coordinator vs Clinical Trial Coordinator

Updated January 8, 2025

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