Clinical research monitor vs clinical trial manager

The differences between clinical research monitors 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 clinical research monitor and a clinical trial manager. Additionally, a clinical trial manager has an average salary of $93,644, which is higher than the $73,325 average annual salary of a clinical research monitor.

The top three skills for a clinical research monitor include FDA, clinical trials and informed consent. The most important skills for a clinical trial manager are patients, clinical trial management, and clinical operations.

Clinical research monitor vs clinical trial manager overview

	Clinical Research Monitor	Clinical Trial Manager
Yearly salary	$73,325	$93,644
Hourly rate	$35.25	$45.02
Growth rate	6%	6%
Number of jobs	98,690	60,284
Job satisfaction	-	-
Most common degree	Bachelor's Degree, 62%	Bachelor's Degree, 60%
Average age	44	44
Years of experience	2	2

What does a clinical research monitor do?

A clinical research monitor monitors all data, observations, information, and feedback from research and experiments. A clinical research monitor is essential in any research laboratory as accurate measurements and collation of data is essential for proper determination and interpretation. In the medical field of study, data accuracy is an absolute necessity as the prescribing of proper medication is only possible if the diagnosis is precise, based on accurate data results of tests. Other additional tasks of a clinical research monitor are organizing data, providing reports, and suggesting improvements in data gathering and monitoring.

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.

Clinical research monitor vs clinical trial manager salary

Clinical research monitors and clinical trial managers have different pay scales, as shown below.

	Clinical Research Monitor	Clinical Trial Manager
Average salary	$73,325	$93,644
Salary range	Between $46,000 And $114,000	Between $61,000 And $142,000
Highest paying City	-	San Rafael, CA
Highest paying state	-	California
Best paying company	-	Editas Medicine
Best paying industry	-	Pharmaceutical

Differences between clinical research monitor and clinical trial manager education

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

	Clinical Research Monitor	Clinical Trial Manager
Most common degree	Bachelor's Degree, 62%	Bachelor's Degree, 60%
Most common major	Nursing	Biology
Most common college	Duke University	University of Pennsylvania

Clinical research monitor vs clinical trial manager demographics

Here are the differences between clinical research monitors' and clinical trial managers' demographics:

	Clinical Research Monitor	Clinical Trial Manager
Average age	44	44
Gender ratio	Male, 29.7% Female, 70.3%	Male, 29.4% Female, 70.6%
Race ratio	Black or African American, 2.6% Unknown, 7.6% Hispanic or Latino, 15.2% Asian, 11.4% White, 62.8% 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 clinical research monitor and clinical trial manager duties and responsibilities

Clinical research monitor example responsibilities.

Manage a consultant to review scientific support and create dossiers on each product that make health claims in the EU.
Maintain CTMS project tracking system of subject and site information and essential documents.
Collect and review all initial regulatory documents from site for submission to IRB and sponsor.
Coordinate and conduct the training of site personnel on protocols, CRF review and conduct source document verification.
Resolve CRF discrepancies and/or clarifications via site visit, telephone, email or fax as deemed appropriate for the study.
Prepare high quality site documents and collect country-specific information for IRB processes.

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.

Clinical research monitor vs clinical trial manager skills

Common clinical research monitor skills

FDA, 12%
Clinical Trials, 11%
Informed Consent, 11%
IRB, 4%
ICH-GCP, 4%
Clinical Operations, 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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Clinical Research Monitor
Clinical Research Monitor vs Clinical Trial Manager

Updated January 8, 2025

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