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Nonclinical Study Monitor Jobs (NOW HIRING)

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site

Conduct clinical study monitoring and/or oversee CRAs to ensure regulatory and protocol compliance as well as overall data accuracy in accordance with the study clinical monitoring plan * Complete ...

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site +1

Conduct clinical study monitoring to ensure regulatory and protocol compliance as well as overall data accuracy in accordance with the study clinical monitoring plan * Complete source data ...

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site +1

Conduct clinical study monitoring to ensure regulatory and protocol compliance as well as overall data accuracy in accordance with the study clinical monitoring plan * Complete source data ...

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site +1

Conduct clinical study monitoring and/or oversee CRAs to ensure regulatory and protocol compliance as well as overall data accuracy in accordance with the study clinical monitoring plan * Complete ...

Zentalis

Sr Clinical Study Manager

San Diego, CA · Remote

... targeted, non-chemo, orally available medicine that enhances treatment experience, choice, and ... Oversee monitoring activities at clinical CROs by reviewing visit reports, protocol deviations and ...

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Nonclinical Study Monitor information

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How much do nonclinical study monitor jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for nonclinical study monitor in the United States is $22.63, according to ZipRecruiter salary data. Most workers in this role earn between $19.23 and $25.00 per hour, depending on experience, location, and employer.

What is a nonclinical study monitor?

Nonclinical Study Monitors are professionals responsible for overseeing the conduct and quality of nonclinical studies, such as toxicology or pharmacology studies, typically conducted before clinical trials in humans. They ensure that studies are performed according to regulatory guidelines, protocols, and Good Laboratory Practice (GLP) standards. Their duties include monitoring data integrity, compliance, and documentation, as well as communicating findings to study sponsors or regulatory authorities. Nonclinical Study Monitors play a crucial role in ensuring that study results are reliable and meet regulatory requirements.

What are the key skills and qualifications needed to thrive as a nonclinical study monitor?

To thrive as a Nonclinical Study Monitor, you generally need a background in life sciences, strong attention to detail, and familiarity with regulatory guidelines such as GLP (Good Laboratory Practice). Experience with data management systems, laboratory information management systems (LIMS), and certifications like RQAP-GLP can be important. Excellent organizational, communication, and problem-solving skills help ensure studies are conducted accurately and findings are clearly reported. These competencies are essential for ensuring compliance, data integrity, and the overall success of nonclinical research projects.

What are some common challenges faced by nonclinical study monitors, and how can these be managed effectively?

Nonclinical Study Monitors often face challenges such as ensuring protocol compliance across multiple study sites, managing large volumes of documentation, and maintaining clear communication between sponsors, laboratories, and regulatory bodies. Staying organized through robust tracking systems and fostering strong professional relationships with site personnel can help address these issues. Additionally, staying up-to-date with regulatory guidelines and participating in ongoing training can further support effective study oversight and compliance.

What is the difference between Nonclinical Study Monitor vs Clinical Research Associate?

AspectNonclinical Study MonitorClinical Research Associate
Required credentialsBachelor's degree in life sciences, certification in Good Laboratory Practice (GLP)Bachelor's degree in health sciences, certification in Good Clinical Practice (GCP)
Work environmentLaboratories, research facilities, pharmaceutical companiesClinical trial sites, hospitals, research centers
Employer and industry usagePharmaceutical, biotech, and contract research organizations (CROs) conducting preclinical studiesPharmaceutical companies, CROs managing clinical trials

While both roles involve monitoring and ensuring compliance, a Nonclinical Study Monitor focuses on preclinical laboratory studies, whereas a Clinical Research Associate oversees clinical trial processes. Both positions require relevant certifications and work in regulated environments, but they serve different stages of drug development.

What states have the most Nonclinical Study Monitor jobs?

States with the most job openings for Nonclinical Study Monitor jobs include:

What are popular job titles related to Nonclinical Study Monitor jobs?

For Nonclinical Study Monitor jobs, the most frequently searched job titles are:

Infographic showing various Nonclinical Study Monitor job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 82% Full Time, 12% Part Time, 4% Contract, and 1% Nights. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $47,067 per year, or $22.6 per hour.

Clinical Study Monitor, Research, Regulatory, & Compliance (Hybrid)

Galveston, TX • Hybrid

UTMB Health
See more jobs at UTMB Healthexternal

Full-time

Re-posted yesterday

Key responsibilities

  • Coordinate and conduct monitoring visits with study teams to assess compliance with protocols, regulations, and safety standards.

  • Develop monitoring plans for IRB-approved studies and ensure timely completion of monitoring activities with documented findings.

  • Assist in preparing study teams for inspections, respond to audit requests, and communicate safety or compliance issues to investigators.

UTMB Health rating

7.2

Company rating: 7.2 out of 10

Based on 172 frontline employees who took The Breakroom Quiz

Job description

EDUCATION & EXPERIENCE

Minimum Qualifications:

  • Bachelor's degree in healthcare administration, nursing, clinical sciences, or related discipline.
  • Five years of clinical experience including three years in clinical research

Preferred Qualifications: (if applicable)

  • Master of Science in Nursing or similar discipline.

JOB SUMMARY

Monitors the administrative components and progress of clinical research studies approved by UTMB Institutional Review Board (IRB). Ensures the safety of clinical trial participants and maintains the accuracy and integrity of trial data.

ESSENTIAL JOB FUNCTIONS

  • Develops and maintains highly collaborative working relationships with internal teams, investigators, and study staff.
  • Assist with the development and dissemination of study-related documents as needed by the research community.
  • Establish monitoring plan for IRB-approved studies including UTMB investigator-initiated projects.
  • Coordinate and conduct monitoring visits with study teams.
  • Ensures timely completion of monitoring activities and creates reports summarizing relevant findings from monitoring visits.
  • Assess the conduct of clinical studies by monitoring compliance with the protocol, federal regulations, and ICH guidelines as applicable, and to ensure safety of human participants, research related evaluations and tests are conducted following the protocol and regulatory requirements and compliance with regulatory agency requirements and institutional policies relating to human participant research.
  • Initiate actions necessary with principal investigators and research teams to correct potential issues identified during monitoring visit, schedule meetings with team to discuss issues concerning scientific integrity and document the findings and action plans.
  • Work with the Office of Research Integrity and Regulatory Affairs 5b(RIRA) and Principal Investigator to escalate study promptly.
  • Notify investigators of any safety or human subject's protection-related findings promptly.
  • Assist in preparing study teams for inspections and with audit responses when requested.

Marginal or Periodic Functions

  • Adheres to internal controls and reporting structure.
  • Performs related duties as required.

KNOWLEDGE/SKILLS/ABILITIES

  • Ability to approach all work activities and interactions with a high level of integrity.
  • Knowledge of regulatory and compliance requirements for clinical research studies including but not limited to, US CFR, ICH, GCP, GDP.
  • Demonstrated excellent presentation, communication (oral and written), teamwork, organizational, interpersonal, and problem-solving skills.
  • Excellent time management and prioritization of tasks to accomplish goals and meet study timelines and deliverables efficiently and successfully.
  • Proven ability to foster effective relationships with teams, functions, partners, and key stakeholders.

WORKING ENVIRONMENT/EQUIPMENT

Standard office environment at UTMB's main campus or other study location.

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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