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Full Time Clinical Research Monitor Jobs (NOW HIRING)

Mass General Brigham

Clinical Research Monitor

Boston, MA · On-site

$50K - $82K/yr

At least 1-2 years of clinical research experience required * Previous experience with monitoring highly preferred Knowledge, Skills, and Abilities * Ability to work independently and as a team ...

Massgeneralbrigham

Clinical Research Monitor

Boston, MA · On-site

$50K - $82K/yr

At least 1-2 years of clinical research experience required * Previous experience with monitoring highly preferred Knowledge, Skills, and Abilities * Ability to work independently and as a team ...

Ohio State University

Clinical Research Monitor - CTSI Department:Health Sciences | Clinical and Translational Science Institute The Ohio State Clinical and Translation Science Institute (CTSI) Research Monitor serves ...

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Full Time Clinical Research Monitor information

What are some common challenges full time clinical research monitors face when overseeing multiple clinical trial sites?

Full Time Clinical Research Monitors often encounter challenges such as coordinating communication across multiple sites, managing diverse site staff, and ensuring consistent adherence to protocols and regulatory requirements. Balancing travel, documentation, and follow-up visits can be demanding, especially when sites are geographically dispersed. Strong organizational skills, attention to detail, and effective relationship-building are crucial to ensuring trials progress smoothly and data integrity is maintained.

What are the key skills and qualifications needed to thrive as a full time clinical research monitor?

To thrive as a Full Time Clinical Research Monitor, you need a solid understanding of clinical trial protocols, Good Clinical Practice (GCP) guidelines, and a background in life sciences or nursing, often supported by a bachelor's degree. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and sometimes certification such as ACRP or SOCRA is highly valuable. Outstanding attention to detail, strong organizational skills, and effective communication are crucial soft skills for ensuring compliance and fostering collaboration among research teams. These competencies are critical for maintaining data integrity, patient safety, and regulatory compliance throughout the clinical trial process.

What is a full time clinical research monitor?

Full Time Clinical Research Monitors, also known as Clinical Research Associates (CRAs), are professionals responsible for overseeing clinical trials to ensure they are conducted according to regulatory requirements, ethical standards, and study protocols. They visit research sites to review data, verify patient records, and ensure participant safety. Their work helps confirm the accuracy and integrity of clinical trial results, playing a critical role in the development of new medical treatments and drugs.
What cities are hiring for Full Time Clinical Research Monitor jobs? Cities with the most Full Time Clinical Research Monitor job openings:
What are the most commonly searched types of Clinical Research Monitor jobs? The most popular types of Clinical Research Monitor jobs are:
What states have the most Full Time Clinical Research Monitor jobs? States with the most job openings for Full Time Clinical Research Monitor jobs include:
Full Time Clinical Research Monitor jobs near you

CLINICAL RESEARCH MONITOR

The Fox Chase Cancer Center Foundation

Philadelphia, PA • On-site, Remote

Full-time

Posted 13 days ago

Job description

The OCR Clinical Research Monitor, completes, revises and reviews the requirements necessary to attaining and maintaining compliance with the FDA and other regulatory bodies for clinical trial research both from a documentation and process level.
Monitors all extramural research program investigator initiated studies being conducted at FCCC and other academic institutions. Ensures protocol compliance at the clinical research sites. Other applicable certification may be considered in lieu of those listed below (i.e

Regulatory Affairs).
Education
Bachelor's Degree Science or other health care discipline Required or
Combination of relevant education and experience may be considered in lieu of degree Required
Experience
2 years experience in clinical research monitoring/auditing Preferred
2 years experience in oncology Preferred
2 years experience working in clinical research Preferred
Licenses
Cert Clin Research Coordinator Preferred or
Cert Clin Research Associate Preferred
Cert Clin Research Prof Preferred

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