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Clinical research monitor vs clinical project manager

The differences between clinical research monitors and clinical project 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 project manager. Additionally, a clinical project manager has an average salary of $100,510, 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 project manager are manage cross, patients, and clinical research.

Clinical research monitor vs clinical project manager overview

Clinical Research MonitorClinical Project Manager
Yearly salary$73,325$100,510
Hourly rate$35.25$48.32
Growth rate6%6%
Number of jobs98,690153,837
Job satisfaction--
Most common degreeBachelor's Degree, 62%Bachelor's Degree, 60%
Average age4444
Years of experience22

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 project manager do?

A clinical project manager specializes in developing and organizing clinical trials. Their responsibilities revolve around planning and coordinating with all necessary personnel and experts, scheduling meetings, and preparing necessary documentation, ensuring compliance with all laws and regulations. Moreover, a clinical project manager must devise strategies and train all staff, develop protocols and guidelines, coordinate with vendors and suppliers, evaluate staff and verify documentation, and assist in all activities to ensure that every process aligns with the project's agenda. Should there be any issues or concerns, a clinical project manager must conduct corrective measures right away.

Clinical research monitor vs clinical project manager salary

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

Clinical Research MonitorClinical Project Manager
Average salary$73,325$100,510
Salary rangeBetween $46,000 And $114,000Between $74,000 And $136,000
Highest paying City-South San Francisco, CA
Highest paying state-California
Best paying company-Intuitive Surgical
Best paying industry-Pharmaceutical

Differences between clinical research monitor and clinical project manager education

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

Clinical Research MonitorClinical Project Manager
Most common degreeBachelor's Degree, 62%Bachelor's Degree, 60%
Most common majorNursingNursing
Most common collegeDuke UniversityUniversity of Pennsylvania

Clinical research monitor vs clinical project manager demographics

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

Clinical Research MonitorClinical Project Manager
Average age4444
Gender ratioMale, 29.7% Female, 70.3%Male, 32.5% Female, 67.5%
Race ratioBlack 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, 7.6% Hispanic or Latino, 15.0% Asian, 10.8% White, 63.6% American Indian and Alaska Native, 0.5%
LGBT Percentage9%9%

Differences between clinical research monitor and clinical project 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.
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Clinical project manager example responsibilities.

  • Develop, manage, motivate and ensure professional development of project staff (13 CRAs).
  • Manage domestic and international oncology clinical study sites.
  • Manage multiple pharmaceutical studies ensuring compliance with FDA guidelines.
  • Manage the operational aspects and execution of clinical studies focusing on oncology.
  • Supervise rotating team of CRA's contract with the CRO, educating on therapeutic area, and ensuring ICH GCP compliance.
  • Ensure GCP / ICH regulatory compliance on studies, preventing study deviations and provide swift resolutions to possible violations.
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Clinical research monitor vs clinical project 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 project manager skills
  • Manage Cross, 12%
  • Patients, 9%
  • Clinical Research, 8%
  • Project Management, 7%
  • Clinical Trials, 5%
  • Oversight, 5%

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