Study coordinator vs clinical trial manager

The differences between study coordinators and clinical trial managers 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 manager. Additionally, a clinical trial manager has an average salary of $93,644, 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 manager are patients, clinical trial management, and clinical operations.

Study coordinator vs clinical trial manager overview

	Study Coordinator	Clinical Trial Manager
Yearly salary	$47,435	$93,644
Hourly rate	$22.81	$45.02
Growth rate	6%	6%
Number of jobs	14,929	60,284
Job satisfaction	-	-
Most common degree	Bachelor's Degree, 61%	Bachelor's Degree, 60%
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 manager do?

A clinical trial manager is primarily responsible for organizing and supervising clinical trials, ensuring to meet all goals while maintaining smooth operations. They are also responsible for collaborating with managers to set targets, hiring staff and participants for studies, and arranging the event. This planning includes its location and schedule. A clinical trial manager must also maintain documentation of all processes, liaise with scientists and key personnel, acquire necessary legal paperwork and certifications, and gather data accurately. Furthermore, as a manager, it is essential to implement the company's policies and regulations at all times.

Study coordinator vs clinical trial manager salary

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

	Study Coordinator	Clinical Trial Manager
Average salary	$47,435	$93,644
Salary range	Between $34,000 And $65,000	Between $61,000 And $142,000
Highest paying City	Oakland, CA	San Rafael, CA
Highest paying state	Connecticut	California
Best paying company	Bloodworks Northwest	Editas Medicine
Best paying industry	Health Care	Pharmaceutical

Differences between study coordinator and clinical trial manager education

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

	Study Coordinator	Clinical Trial Manager
Most common degree	Bachelor's Degree, 61%	Bachelor's Degree, 60%
Most common major	Nursing	Biology
Most common college	University of Michigan - Ann Arbor	University of Pennsylvania

Study coordinator vs clinical trial manager demographics

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

	Study Coordinator	Clinical Trial Manager
Average age	44	44
Gender ratio	Male, 23.7% Female, 76.3%	Male, 29.4% Female, 70.6%
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, 7.5% Hispanic or Latino, 14.9% Asian, 11.1% White, 63.4% American Indian and Alaska Native, 0.5%
LGBT Percentage	9%	9%

Differences between study coordinator and clinical trial manager 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 manager example responsibilities.

Manage SAEs and assure they are properly record and report.
Manage CRO vendors and ensure timely execution of study milestones.
Manage assign independent consultants and employee CRAs regarding project-relate issues.
Lead study data management activities for oncology trials in preparation for study close-out.
Ensure study adherence to all regulatory matters and sponsor requirements according to FDA regulations, GCP and ICH guidelines.
Create document templates require by FDA and ICH regulations for site distribution.

Study coordinator vs clinical trial manager skills

Common study coordinator skills

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

Common clinical trial manager skills

Patients, 8%
Clinical Trial Management, 7%
Clinical Operations, 6%
Clinical Research, 6%
Oversight, 6%
Project Management, 5%

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Study Coordinator
Study Coordinator vs Clinical Trial Manager

Updated January 8, 2025

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