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Nonclinical Study Monitor Jobs (NOW HIRING)

Kps-Life

Sr. Clinical Study Lead (Hybrid)

Cambridge, MA · On-site

Monitors progress for site activation and monitoring visits and acts on any deviations from plan ... non-compliance by sites. * Oversees and ensures the CROs and Third Party Vendors are in alignment ...

New

Altasciences

Study Director

Everett, WA

$79K - $120K/yr

Coordinates all phases of a non-clinical study in collaboration with internal departments, external ... Monitors, tracks, and communicates study milestones effectively to all contributors (internal and ...

ARTHREX

Sr. Clinical Study Manager

Naples, FL · On-site

Maintain appropriate monitoring and maintenance of clinical sites to ensure the overall successful conduct of assigned clinical studies. * Oversee all aspects of the assigned clinical projects ...

Arthrex

Sr. Clinical Study Manager

Naples, FL · On-site

Maintain appropriate monitoring and maintenance of clinical sites to ensure the overall successful conduct of assigned clinical studies. * Oversee all aspects of the assigned clinical projects ...

Arthrex GmbH

Sr. Clinical Study Manager

Naples, FL · On-site

Maintain appropriate monitoring and maintenance of clinical sites to ensure the overall successful conduct of assigned clinical studies. * Oversee all aspects of the assigned clinical projects ...

Kps-Life

Clinical Study Specialist

Cambridge, MA · On-site

Clinical Study Specialist - (Armonk, NY, Cambridge MA or Warren, NJ) Warren, NJ, Armonk, NY or ... Monitor and update investigator and site status throughout the trial. * Support clinical trial ...

System One

Clinical Study Manager

Durham, NC · On-site

Monitor adherence to essential document collection processes, site activation requirements, clinical supply release requirements, and study-specific tracking tools. * Support and/or lead meetings ...

System One

Clinical Study Manager

Durham, NC · On-site

Monitor adherence to essential document collection processes, site activation requirements, clinical supply release requirements, and study-specific tracking tools. * Support and/or lead meetings ...

TalentBurst, Inc.

Clinical Study Manager

Durham, NC · On-site

... Monitor adherence to essential document collection processes, site activation requirements, clinical supply release requirements, and study-specific tracking tools. " Support and/or lead meetings ...

Regeneron

Clinical Study Associate Manager

Warren, NJ · On-site

Monitors recruitment and retention, and monitors progress for site activation and monitoring visits ... non-compliance by sites, and escalates data flow and data quality issues to Clinical Study Lead

New

System One

Clinical Study Manager

Durham, NC · On-site

Monitor adherence to essential document collection processes, site activation requirements, clinical supply release requirements, and study-specific tracking tools. * Support and/or lead meetings ...

System One

Clinical Study Manager

Durham, NC · On-site

Monitor adherence to essential document collection processes, site activation requirements, clinical supply release requirements, and study-specific tracking tools. * Support and/or lead meetings ...

MMS

Senior Nonclinical Writer (US)

Canton, MI · On-site

Ability to develop a mapping plan for the placement of nonclinical studies within structure of Module 2.4 and 2.6 eCTD submission documents. * Interpret and analyze applicable pharmacokinetics ...

System One

Clinical Study Manager

Durham, NC · On-site

Monitor adherence to essential document collection processes, site activation requirements, clinical supply release requirements, and study-specific tracking tools. * Support and/or lead meetings ...

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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, 83% Full Time, 12% Part Time, 3% Contract, and 1% Nights. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $47,067 per year, or $22.6 per hour.

Senior Manager, Clinical Study Lead

Tarrytown, NY • On-site

Regeneron Pharmaceuticals, Inc.
Biotechnology Research and Development • 5 - 10K employees
Learn more about Regeneron Pharmaceuticals, Inc.external

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 12 days ago

Regeneron rating

8.6

Company rating: 8.6 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

Job description

Build our future together:
At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Clinical Study Lead to join our Clinical Trial Management team, supporting our Inflammation & Immunology therapeutic area. The Senior Clinical Study Lead (CSL) is expected to operate with high-degree of independence and is accountable for the global execution of assigned large and/or complex clinical trials from study design, through execution, to study close out. You will be accountable for the study timelines, study budget, and ensuring study conduct is in accordance with Regeneron Standard Operating Procedures (SOPs) and ICH/GCP. This role applies to internally sourced studies and studies out-sourced to Clinical Research Organizations (CROs) and the balance of direct leadership versus oversight will vary accordingly.
When & where:
  • Work Location: Armonk, NY, Warren, NJ
  • Work Model: Primarily on-site with hybrid flexibility
  • Travel: 25% Travel may be required

Discover your role:
  • Leads the cross-functional study team responsible for clinical study delivery and is the primary point of contact of leadership and oversight (as required) for the assigned study
  • Oversees and provides input to the development of study specific documentation including but not limited to: case report forms (CRF), data management plan, monitoring plan, monitoring oversight plan, project specific training plan, data review plan, statistical analysis plan, etc.
  • Oversees set-up and maintenance of study systems including but not limited to Clinical Trial Management System (CTMS), Trial Master File (TMF) etc.
  • Identifies outsourcing needs of the study and leads and oversees engagement, contracting and management of required vendors
  • Provides input into baseline budget development and management; Provides input into baseline timeline development and management
  • Leads risk assessment and identifies risk mitigation strategies at the study level; Leads the feasibility assessment to select relevant regions and countries for the study
  • Monitors progress for site activation and monitoring visits and acts on any deviations from plan
  • Leads the development of and oversees implementation of patient recruitment and retention strategies and acts on any deviations from plan; Monitors data entry and query resolution and acts on any deviations from agreed metrics
  • Oversees and provides input to the study drug and clinical supplies forecasting, drug accountability and drug reconciliation
  • Escalates issues related to study conduct, quality, timelines or budget to Program Operations Leader (POL) and other stakeholders and develops and implements appropriate actions to address issues
  • Manages and oversees study close-out activities including but not limited to database lock, reconciliation of vendor contracts, budget, TMF, and study drug accountability
  • May be assigned unmasked tasks for studies, which may include but is not limited to, assisting with masked investigational product, set up and management of unmasked trial master file, review of unmasked data in the electronic data capture system, point of contact for IVRS issues, and support oversight of unmasked clinical monitoring
  • Responsible for direct supervision of CTM staff. Line management responsibilities include work assignments, performance management, staff recruitment, professional development, coaching, mentoring, ongoing training and compliance, and study support/oversight

This role requires:
  • A minimum of a Bachelor's degree is required and a minimum of 8 years relevant clinical trial experience
  • We are seeking experience with line management as well as exceptional interpersonal and leadership skills
  • Proactive and self-disciplined, ability to meet deadlines, effective use of time, and prioritization; Ability to influence and negotiate across a wide range of stakeholders
  • Advanced technical proficiency in trial management systems and MS applications including (but not limited to) Project, PowerPoint, Word, Excel, IVRS/IWRS, EDC
  • We are seeking extensive experience in global clinical trial operations with unique knowledge and skills to contribute to the development of protocols and key study documents
  • Applies advanced expertise and implements the operational strategic direction and guidance for respective clinical studies

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.
Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.
Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about on-site expectations for your role and location.
As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.
For jobs in Canada: this posting is for an existing position.
Salary Range (annually)
$150,500.00 - $245,500.00

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