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Preclinical Study Monitor Jobs (NOW HIRING)

Research Post Doctoral Fellow

Phoenix, AZ · On-site

$46K - $63K/yr

... monitors daily project protocols ensuring adherence to study timelines and objectives. • Contributes to the development of preclinical trial plans including experimental design methodology and ...

Experience managing CRO relationships for outsourced preclinical and GLP studies, including vendor qualification, protocol development, monitoring, and report review.Proven ability to lead, mentor ...

Project Manager R&D

Jersey City, NJ · Hybrid

$125K - $150K/yr

The primary focus of the role will be outsourced preclinical studies, including pharmacology ... Track program budgets, monitor expenditures, forecast spend, and identify cost-saving opportunities ...

The Study Coordinator is responsible for providing highlevel organizational support for preclinical ... monitoring the in-life progress of assigned studies, and interacting with clients. * Provides ...

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Preclinical Study Monitor information

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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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What cities are hiring for Preclinical Study Monitor jobs?

Cities with the most Preclinical Study Monitor job openings:

What are the most commonly searched types of Preclinical Study Monitor jobs?

The most popular types of Preclinical Study Monitor jobs are:

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.

Research Post Doctoral Fellow

St Joseph Hospital & Medical Center

Phoenix, AZ • On-site

$24.33 - $36.19/hr

Full-time

Re-posted 20 days ago


Job description


Job Summary and Responsibilities

The Ivy Brain Tumor Center is a non-conventional non-profit program offering state-of-the-art clinical trials for patients with the most aggressive form of brain cancer. It is home to the largest collection of Phase 0 trials for brain tumors in the world. Our multidisciplinary team of brain tumor specialists and scientists are accelerating drug discovery and precision medicine in neuro-oncology to identify the most promising first-in-class therapies for brain tumor patients.

As a Research Post Doctoral Fellow, you will actively engage in laboratory, translational, or clinical research under faculty guidance. Your primary objective is to advance your specialized understanding and practical skills.
Every day you will contribute to ongoing research by conducting experiments, analyzing data, or participating in clinical investigations. This experience aims to build competencies for independent investigative work.
To be successful in this role, you will demonstrate strong foundational knowledge, a proactive research approach, and commitment to developing independence and critical thinking.

  • Aspires to excellence in work quality and quantity.
  • Shows growth technically and intellectually.
  • Contributes to mentor-directed research.
  • Demonstrates capabilities to produce quality original research or clinical care.
  • Develops skills in a research and/or clinical specialty
  • Demonstrates potential to launch an extramurally-funded research program.

The Ivy Brain Tumor Center seek a motivated and skilled Postdoctoral Fellow to join a dynamic collaborative research team focused on advancing preclinical neurooncology research. This position offers an exceptional opportunity to contribute to cutting-edge glioma research develop independent scientific expertise and build a foundation for a successful research career. The successful candidate will design and execute preclinical studies mentor junior laboratory staff and actively contribute to scholarly dissemination of research findings. 

• Designs conducts and analyzes both in vitro and in vivo experiments using established and novel glioma models

• Plans organizes and monitors daily project protocols ensuring adherence to study timelines and objectives.

• Contributes to the development of preclinical trial plans including experimental design methodology and outcome measures.

• Applies and maintains Good Laboratory Practice (GLP) standards in all aspects of research including collection preparation and maintenance of required research documentation and final preclinical study reports.

• Supervises and provides mentorship and training to laboratory research staff fostering a culture of scientific rigor and professional growth

• Coordinates and collaborates with interdisciplinary Ivy Center teams to advance preclinical research projects and ensure alignment of shared objectives

• Maintains current knowledge of the field by reviewing and critically evaluating scientific literature integrating emerging findings into ongoing research efforts Scholarly communication and dissemination

• Leads and contributes to the preparation and submission of abstracts and peer-reviewed manuscripts for publication

• Assists in the preparation of grant proposals and funding applications including literature reviews preliminary data synthesis and scientific narrative development.

• Prepares and delivers research presentations at internal meetings institutional seminars and regional national and international scientific conferences. 

For more information on the in vivo/in vitro team please see: https://www.ivybraintumorcenter.org/research/labs/mehta-laboratory/

Job Requirements

Required

  • Doctoral degree (PhD) or equivalent in a relevant field of endeavor 
  • Laboratory or clinical research at the post-baccalaureate level with an interest in a faculty member's line of study


Preferred

  • Experience writing research reports concerning own work and familiarity with a biomedical discipline
Where You'll Work
Hello Humankindness: Join a Legacy of Healing at Saint Joseph’s Hospital and Medical Center (SJHMC) Ready to make a real difference? Join SJHMC in Phoenix AZ., a 571-bed nonprofit founded by the Sisters of Mercy over 125 years ago. We're more than a hospital; we're a global destination for life-changing care, embracing patients with humankindness.

Here, your calling will flourish. We're not just a workplace; we're a community dedicated to a mission of service.

Leaders in Specialized Care:

  • Barrow Neurological Institute (BNI): A world-renowned center for groundbreaking neurological research and innovative treatments.
  • Norton Thoracic Institute (NTI): A national leader in advanced thoracic care with pioneering surgical techniques.
  • Level I Trauma Center: One of Arizona's busiest ERs, providing immediate, comprehensive care for critically injured patients 24/7.

Why SJHMC?

  • Culture of Excellence & Well-being: We care for our people, fostering professional and personal growth.
  • Community & Collaboration: Be part of a network committed to global health and well-being.
  • Join a Legacy, Shape a Future: Over 20% of our patients travel internationally for our specialized care.

This is an invitation to join a family of dedicated professionals at the forefront of medical innovation, united by the power of humankindness.

Qualifications:

Required

  • Doctoral degree (PhD) or equivalent in a relevant field of endeavor 
  • Laboratory or clinical research at the post-baccalaureate level with an interest in a faculty member's line of study


Preferred

  • Experience writing research reports concerning own work and familiarity with a biomedical discipline
Employment Type: Full Time