Clinical research monitor vs clinical researcher

The differences between clinical research monitors and clinical researchers 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 researcher. Additionally, a clinical research monitor has an average salary of $73,325, which is higher than the $55,453 average annual salary of a clinical researcher.

The top three skills for a clinical research monitor include FDA, clinical trials and informed consent. The most important skills for a clinical researcher are patients, informed consent, and IRB.

Clinical research monitor vs clinical researcher overview

	Clinical Research Monitor	Clinical Researcher
Yearly salary	$73,325	$55,453
Hourly rate	$35.25	$26.66
Growth rate	6%	6%
Number of jobs	98,690	60,864
Job satisfaction	-	-
Most common degree	Bachelor's Degree, 62%	Bachelor's Degree, 58%
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 researcher do?

A clinical researcher is primarily in charge of conducting research trials for medicine and health care development. Their responsibilities mainly revolve around conducting extensive research and analysis by gathering samples, performing experiments, working with research participants, and collaborating with other researchers and scientists. Moreover, as a clinical researcher, it is essential to maintain records of all experiments, summarize findings into reports and presentations, and monitor every progress, all while adhering to the research's deadlines, budgets, goals, and policies.

Clinical research monitor vs clinical researcher salary

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

	Clinical Research Monitor	Clinical Researcher
Average salary	$73,325	$55,453
Salary range	Between $46,000 And $114,000	Between $38,000 And $79,000
Highest paying City	-	Santa Rosa, CA
Highest paying state	-	California
Best paying company	-	Edwards Lifesciences
Best paying industry	-	Pharmaceutical

Differences between clinical research monitor and clinical researcher education

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

	Clinical Research Monitor	Clinical Researcher
Most common degree	Bachelor's Degree, 62%	Bachelor's Degree, 58%
Most common major	Nursing	Biology
Most common college	Duke University	University of Michigan - Ann Arbor

Clinical research monitor vs clinical researcher demographics

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

	Clinical Research Monitor	Clinical Researcher
Average age	44	44
Gender ratio	Male, 29.7% Female, 70.3%	Male, 38.3% Female, 61.7%
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, 2.5% Unknown, 7.4% Hispanic or Latino, 14.0% Asian, 13.5% White, 62.2% American Indian and Alaska Native, 0.5%
LGBT Percentage	9%	9%

Differences between clinical research monitor and clinical researcher 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 researcher example responsibilities.

Manage site master file contents and work with sites to ensure communication requirements between site and IRB are adhere to.
Establish and maintain strong community partnerships to achieve HIV prevention objectives.
Maintain study database to in compliance with FDA regulations.
Perform NIH studies, coordinate interviews of clinical research trial participant's.
Support IRB applications and analyze collected data.
Interact with and assess patients to determine effectiveness of medicine.

Clinical research monitor vs clinical researcher skills

Common clinical research monitor skills

FDA, 12%
Clinical Trials, 11%
Informed Consent, 11%
IRB, 4%
ICH-GCP, 4%
Clinical Operations, 4%

Common clinical researcher skills

Patients, 16%
Informed Consent, 12%
IRB, 10%
Clinical Trials, 8%
Data Collection, 8%
FDA, 6%

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Clinical Research Monitor
Clinical Research Monitor vs Clinical Researcher

Updated January 8, 2025

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