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Clinical Research Associate Monitor Jobs (NOW HIRING)

ICON

Clinical Research Associate - St Louis/Kansas City/Ohio ICON plc is a world-leading healthcare ... Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.

ICON

Clinical Research Associate

Clinical Research Associate ICON plc is a world-leading healthcare intelligence and clinical ... Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.

ICON

Clinical Research Associate - Baltimore, MD/Philadelphia, PA ICON plc is a world-leading healthcare ... Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.

ICON

Clinical Research Associate

Clinical Research Associate - Multi TA/Oncology - US ICON plc is a world-leading healthcare ... Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.

ICON

Clinical Research Associate

Clinical Research Associate - Multi TA/Oncology - US ICON plc is a world-leading healthcare ... Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.

Eisenhower

Clinical Research Associate

Rancho Mirage, CA

$20.71 - $31.30/hr

Certification from Society of Clinical Research Associate (SOCRA) as a Certified Clinical Research ... monitor/IRB.7. Reports serious adverse events.8. Handles and maintains investigator files.9. ...

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How much do clinical research associate monitor jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for clinical research associate monitor in the United States is $41.13, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $52.64 per hour, depending on experience, location, and employer.

What are some common challenges Clinical Research Associate Monitors face when overseeing multiple clinical trial sites?

Clinical Research Associate Monitors often manage several clinical trial sites simultaneously, which can present challenges such as coordinating schedules, ensuring consistent protocol adherence, and managing documentation across diverse teams. Effective communication and strong organizational skills are crucial to address site-specific issues promptly and maintain regulatory compliance. Additionally, frequent travel and adapting to varying site cultures are common aspects of the role, and building strong relationships with site staff can greatly enhance trial success.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate Monitor, and why are they important?

To thrive as a Clinical Research Associate Monitor, you need a solid understanding of clinical trial protocols, regulatory guidelines (such as GCP and FDA regulations), and often a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like ACRP or SOCRA are typically required. Excellent attention to detail, strong organizational skills, and effective communication are crucial soft skills for liaising with site staff and ensuring protocol compliance. These competencies ensure that clinical trials are conducted ethically, accurately, and in adherence to regulatory standards, safeguarding data integrity and patient safety.

What is a Clinical Research Associate Monitor?

A Clinical Research Associate Monitor is a professional responsible for overseeing clinical trials to ensure they are conducted in accordance with regulatory requirements, Good Clinical Practice (GCP) guidelines, and study protocols. They monitor trial sites, review documentation, verify data accuracy, and ensure the safety and rights of study participants. Their work is crucial in maintaining the integrity of clinical research and facilitating the development of new medical treatments.
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Clinical Research Associate Monitor jobs near you
Clinical Research Associate II

Clinical Research Associate II

University of Nebraska Medical Center

Omaha, NE • On-site

$43K - $65K/yr

Full-time

Posted 29 days ago

University Of Nebraska Medical Center rating

8.5

Company rating: 8.5 out of 10

Based on 15 frontline employees who took The Breakroom Quiz

48th of 995 rated hospitals

Job description

GENERAL REQUISITION INFORMATION
EEO Statement:
UNMC is an Equal Employment Opportunity Employer, including an equal opportunity employer of protected veterans and individuals with disabilities.
Location Omaha, NE Requisition Number: Staff_14714 Department Ophthalmology and Visual Sciences 50000516 Business Unit College of Medicine Reg-Temp Full-Time Regular Work Schedule Monday - Friday: 8:00 AM - 5:00 PM Remote/Telecommuting No remote/telecommuting opportunity Position Summary
Responsible for research activities, data management and carrying out day to day research project activities. Responsible for monitoring progress of research protocol for multi-center study and collection of research data on patients enter into research protocols in the Department of Ophthalmology. This position works on clinical studies, which require a high level of knowledge, coordination, and data abstraction.
Position Details
Additional Information
Posting Category Research - Non Academic Working Title Clinical Research Associate II Job Title Clincal Research Associate L2 Salary Grade RA15S Appointment Type B1 - REG MGR PROF SALARY Salary Range $43,800 - $65,700/annual Job Requisition Begin Date 04/30/2026 Application Review Date 05/11/2026 Review Date Information:
Initial application review will begin on the date provided in the field above. Applications received prior to this review date will be considered. Applications received after the review date may be considered.
Required and Preferred Qualifications
Required Education: Associate's degree or equivalent If any degree major/training is required, please specify the type. (NOTE: Concentration and minors are not equivalent to a major)
Healthcare, Science or related field
(Will consider four years related education/ experience)
Required Experience 2 years If any experience is required, please specify what kind of experience:
Experience related to healthcare, laboratory and/or clinical research
(Will consider four years related education/ experience)
Required License No If yes, what is the required licensure/certification? Required Computer Applications: Microsoft Access, Microsoft Excel Required Other Computer Applications: Required Additional Knowledge, Skills and Abilities:
1. Knowledge of clinical research practices and principles required.
2. Highly effective verbal communication and interpersonal skills required.
3. Must be able to independently assimilate and evaluate clinical data.
4. Must be familiar with medical ophthalmology terminology.
5. Must be able to handle multiple tasks at once.
6. Must have excellent communication skills and work well in a group setting.
Preferred Education: Bachelor's degree If any degree/training is preferred, please specify the type:
Healthcare, Science, Engineering, or related field.
Preferred Experience:
Experience with completing Case Report Forms
(CRF's) and creating source documents a plus.
Preferred License: Yes If yes, what is the preferred licensure/certification?:
Certified Ophthalmic Technician (COT)
Phlebotomy certification
Preferred Computer Applications: Preferred Other Computer Applications: Preferred Additional Knowledge, Skills and Abilities: Email to a Friend https://unmc.peopleadmin.com/postings/97803

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