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Preclinical Study Monitor Jobs (NOW HIRING)

RPM ReSearch

Study Director

West Sacramento, CA

$74K - $110K/yr

Study Director, Research Scientist Are you passionate about preclinical research? As a Study ... Monitor study milestones and ensure accurate recording and verification of all experimental data.

Inotivco

Study Director III, Toxicology

Mount Vernon, IN · On-site

Monitor the progress of studies and after consultation with senior staff, report the results to the ... Inform the management of any issues affecting the conduct of preclinical studies, interaction with ...

Inotiv

Study Director III, Toxicology

Mount Vernon, IN · On-site

Monitor the progress of studies and after consultation with senior staff, report the results to the ... Inform the management of any issues affecting the conduct of preclinical studies, interaction with ...

Inotiv

Study Director III, Toxicology

Mount Vernon, IN · On-site

Monitor the progress of studies and after consultation with senior staff, report the results to the ... Inform the management of any issues affecting the conduct of preclinical studies, interaction with ...

NAMSA

Associate Study Director

Northwood, OH

Serves as the Study Director for GLP and non-GLP preclinical studies and assures that all ... monitors. The Associate must occasionally lift and/or move up to 50 pounds. Specific vision ...

University of Utah

Laboratory Technicians

Campus, IL · On-site

$10 - $22/hr

Job Responsibilities The Lab Technician will assist with a variety of preclinical cancer research activities, including: Animal study support * Perform routine animal husbandry, monitoring, and study ...

University of Utah

Laboratory Technicians

Campus, IL

$10 - $22/hr

Job Responsibilities The Lab Technician will assist with a variety of preclinical cancer research activities, including: Animal study support * Perform routine animal husbandry, monitoring, and study ...

University of Utah

Laboratory Technicians

Campus, IL · On-site

$10 - $22/hr

Job Responsibilities The Lab Technician will assist with a variety of preclinical cancer research activities, including: Animal study support * Perform routine animal husbandry, monitoring, and study ...

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How much do preclinical study monitor jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for preclinical study monitor in the United States is $25.32, according to ZipRecruiter salary data. Most workers in this role earn between $21.88 and $26.92 per hour, depending on experience, location, and employer.

What is a preclinical study monitor?

A Preclinical Study Monitor oversees non-clinical research studies to ensure regulatory compliance, data integrity, and adherence to study protocols. They work closely with contract research organizations (CROs), laboratories, and internal teams to monitor study progress, resolve issues, and ensure high-quality study outcomes. Their role is critical in evaluating the safety and efficacy of drug candidates before they proceed to clinical trials.

What are the typical responsibilities and daily tasks of a preclinical study monitor?

As a Preclinical Study Monitor, you are primarily responsible for overseeing the progress of preclinical studies to ensure adherence to study protocols, industry regulations, and quality standards. Your daily tasks can include reviewing study documentation, inspecting laboratory processes, communicating with research teams, and resolving discrepancies or compliance issues. You'll often collaborate with scientists, laboratory technicians, and regulatory personnel to facilitate smooth study execution. Expect to spend time both at the laboratory site and completing documentation or follow-ups remotely. This role requires a proactive approach to problem-solving and frequent, detail-oriented communication to drive the success of preclinical research projects.

What are the key skills and qualifications needed to thrive in the preclinical study monitor position, and why are they important?

To thrive as a Preclinical Study Monitor, you need a solid background in life sciences, familiarity with Good Laboratory Practice (GLP) standards, and experience in preclinical research or drug development. Knowledge of laboratory management software, data collection systems, and industry certifications such as AALAS or RA certification can be highly beneficial. Attention to detail, strong organizational skills, and effective communication set outstanding candidates apart. These abilities are crucial for ensuring study compliance, maintaining data integrity, and facilitating smooth collaboration between research teams and regulatory bodies.

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Preclinical Study Monitor jobs near you
Infographic showing various Preclinical Study Monitor job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $52,672 per year, or $25.3 per hour.

Study Director

RPM ReSearch

West Sacramento, CA

$74K - $110K/yr

Full-time

Re-posted 6 days ago

Job description

Join Our Team as a Study Director and Research Scientist!

Your New Opportunity: We're all about teamwork. Every role contributes to the discovery, development, and manufacturing of new drug therapies, helping us get them to the people who need them faster. By living our values—Employee Development, Customer Focus, Quality and Excellence, Respect, and Integrity—we create a passionate, collaborative work environment. Whether you’re a recent graduate or seeking your next career move, your future could be with us.


Why Join Us?

  • Impactful Work: Play a significant role in global health and well-being.
  • Collaborative Environment: Work with a team that values your input and expertise.
  • Growth Opportunities: Whether you’re just starting your career or looking to advance, we offer a dynamic environment to grow and thrive.


The Role: Study Director, Research Scientist Are you passionate about preclinical research? As a Study Director, you’ll be the single point of control for assigned studies, responsible for the interpretation, analysis, documentation, and reporting of study results for both GLP and non-GLP studies.


What You’ll Do:

  • Oversee the technical conduct of studies and manage the interpretation, analysis, and reporting of results.
  • Perform duties following GLPs and other relevant regulations.
  • Collaborate with sponsors, study directors, and others to optimize protocol design.
  • Coordinate study schedules and logistics with clients, subcontractors, and internal departments.
  • Ensure study personnel are properly trained and educated for their roles.
  • Monitor study milestones and ensure accurate recording and verification of all experimental data.
  • Communicate ongoing study activities and results to sponsors.
  • Analyze and interpret study data, preparing comprehensive study reports.
  • Maintain documentation, protocols, and study reports, ensuring all are archived appropriately.
  • Review, revise, and write SOPs as necessary.


What You Need to Succeed:

  • Education: Master’s or Doctoral Degree in a relevant scientific discipline (or equivalent experience).
  • Experience: 3+ years as a Study Director for in vivo studies in a biopharmaceutical company or CRO. Experience in Toxicology is a plus.
  • Skills: Intermediate to Advanced Computer Skills, strong planning and organizational skills, ability to manage change, and effective communication of scientific data.
  • Other: Must complete Study Director Training and maintain ongoing scientific and professional education.