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Overnight Clinical Research Monitor Jobs (NOW HIRING)

The Ridge RTC

Overnight Clinical Assistant

Milton, NH · On-site

Job Summary As an Overnight Residential Clinical Assistant at Paradigm Treatment Centers and Ridge ... Supervise and monitor client activities overnight, including preparation for quiet hours, sleep ...

Quality Clinical Research,

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Clinical Research Coordinator

Omaha, NE · On-site

$24 - $29/hr

Clinical Research Coordinator Location: Omaha NE Position Type: Full-Time, On-Site We are seeking a ... monitors, and internal team members * Maintain regulatory binders and study records * Support ...

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Overnight Clinical Research Monitor information

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$39

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

As of Aug 6, 2026, the average hourly pay for overnight clinical research monitor in the United States is $38.70, according to ZipRecruiter salary data. Most workers in this role earn between $38.22 and $39.18 per hour, depending on experience, location, and employer.

What is the difference between Overnight Clinical Research Monitor vs Clinical Research Coordinator?

AspectOvernight Clinical Research MonitorClinical Research Coordinator
CredentialsTypically requires a degree in health sciences or related field, plus monitoring certificationsUsually holds a bachelor's degree in health or science, with some roles requiring certification
Work EnvironmentPrimarily remote or site-based, overseeing multiple sites, often during off-hoursOn-site at clinical trial locations, managing daily trial activities
Employer & IndustryPharmaceutical companies, CROs, research institutionsHospitals, clinics, research centers

The Overnight Clinical Research Monitor focuses on overseeing trial compliance remotely, often during night hours, while the Clinical Research Coordinator manages daily trial activities on-site. Both roles require health-related credentials but differ in work hours and environment.

What cities are hiring for Overnight Clinical Research Monitor jobs? Cities with the most Overnight 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 Overnight Clinical Research Monitor jobs? States with the most job openings for Overnight Clinical Research Monitor jobs include:
Overnight Clinical Research Monitor jobs near you

Clinical Research Coach (Onsite) Research Administration (Galveston) Certification (CCRC)

UTMB Health

Galveston, TX • On-site

$22.75 - $30.25/hr

Other

Re-posted 26 days ago

UTMB Health rating

7.3

Company rating: 7.3 out of 10

Based on 168 frontline employees who took The Breakroom Quiz

267th of 887 rated healthcare providers

Job description

Minimum Qualifications:

Bachelor's degree and 7 years of experience with interventional clinical research or equivalent.  Certified Clinical Research Professional (CCRP) or Certified Clinical Research Coordinator (CCRC) or similar certification through a recognized professional clinical research organization, or ability to obtain professional certification within one year of employment.


Preferred Qualifications:

  • Registered Nurse or Medical Degree.
  • Clinical Research Monitor or Coordinator experience.
  • Experience with a Clinical Trial Management System (CTMS), electronic IRB platform, and EMR.

Job Description:  


The primary focus of the Clinical Research Coach is to provide mentorship, instruction, and guidance to clinical research investigators, nurses, coordinators, and other study staff to promote high-quality research and implement best practices. This position focuses on the operational aspects of compliant study conduct, including recruitment, enrollment, consent process, study visit completion, source documentation, data collection, and reporting. 

Job Duties:

  • Review and comprehend the scientific and operational aspects of clinical research protocols, including but not limited to the study purpose, schema, procedures, eligibility criteria, and study timelines.

  • Work closely with assigned investigators and study teams throughout the entire study lifecycle 

    to: 

    • Provide insight and feedback on IRB regulatory submission requirements, documents, and overall processes.

    • Provide resources and best practices for developing source documents, protocol-specific flowsheets, case report forms (CRFs), enrollment logs, and deviation logs.

    • Provide tools, processes, and training to promote regulatory and protocol compliance as it relates to subject recruitment, the consent process, subject eligibility, study visits, subject and regulatory documentation standards.

    • Provide training and review of essential documents and creating/maintaining a regulatory binder.

    • Accompany investigators and study staff for initial consent processes and study visits to provide support and feedback.

    • Review initial study documentation to ensure it is attributable, legible, contemporaneous, original, accurate, and complete.

    • Prepare for monitoring and/or audits.

  • Quickly identify when a Sponsor, Investigator, or Institution should be alerted to concerns or issues.

  • Collaborate with the Office of Institutional Compliance and the Office of Research Regulations and Compliance.

  • Adheres to internal controls and reporting structure.

  • Performs related duties as required.

Working Environment/Equipment 

  • Standard hospital, clinical, and/or laboratory areas where clinical research may occur.
  • Standard office environment.
  • Standard office equipment. Microsoft Office Suite.

Salary Range:

Actual salary commensurate with experience.

EQUAL EMPLOYMENT OPPORTUNITY:

UTMB Health strives to provide equal opportunity employment without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, genetic information, disability, veteran status, or any other basis protected by institutional policy or by federal, state or local laws unless such distinction is required by law. As a Federal Contractor, UTMB Health takes affirmative action to hire and advance protected veterans and individuals with disabilities.

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