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Remote Site Monitor Jobs in Colorado (NOW HIRING)

Restaurant365

Site Reliability Engineer II

Denver, CO · On-site +1

$98K - $138K/yr

Enhance and evolve monitoring tools and platforms to improve observability. * Promote and apply ... Wellness initiatives #BI-Remote Internal Employees - R365 is committed to growing talent from ...

Restaurant365

Site Reliability Engineer II

Denver, CO · On-site +1

$98K - $138K/yr

Enhance and evolve monitoring tools and platforms to improve observability. * Promote and apply ... Wellness initiatives #BI-Remote Internal Employees - R365 is committed to growing talent from ...

CPC

Sr. Clinical Operations Manager

Aurora, CO · On-site +1

Remote candidates are welcome to apply. General Responsibilities: * Work closely with the Head of ... negotiation, and site monitoring processes as required by contract. * Identify the required ...

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Remote Site Monitor information

See Colorado salary details

$12

$26

$41

How much do remote site monitor jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for remote site monitor in Colorado is $26.19, according to ZipRecruiter salary data. Most workers in this role earn between $20.72 and $28.32 per hour, depending on experience, location, and employer.

What is a remote site monitor?

A Remote Site Monitor (RSM) is a clinical research professional responsible for overseeing and ensuring compliance at clinical trial sites without being physically present. They review site documentation, verify data accuracy, and monitor patient safety through remote communication and electronic systems. RSMs work closely with site staff to ensure adherence to protocols, Good Clinical Practice (GCP), and regulatory requirements. This role helps streamline trial oversight while reducing the need for on-site visits. Effective communication, attention to detail, and familiarity with clinical trial processes are essential for success in this position.

What are the key skills and qualifications needed to thrive as a remote site monitor, and why are they important?

To excel as a Remote Site Monitor, you should possess strong analytical skills, attention to detail, and typically have a background in clinical research, life sciences, or a related field. Familiarity with electronic data capture (EDC) systems, remote monitoring platforms, and certifications such as GCP (Good Clinical Practice) are often required. Excellent communication, organizational skills, and the ability to work independently set top candidates apart. These skills are crucial for ensuring regulatory compliance, data integrity, and effective site management from a remote location.

What are some typical challenges faced by a remote site monitor, and how can they overcome them?

Remote Site Monitors often face challenges such as limited on-site visibility, ensuring timely communication with site staff, and verifying data accuracy without physical presence. Utilizing robust technology platforms, establishing clear communication protocols, and building strong relationships with site teams can help overcome these obstacles. Being proactive and adaptable is key to efficiently resolving issues and maintaining high-quality standards. Staying organized and detail-oriented also helps monitors prioritize workload and meet important study deadlines.

What are popular job titles related to Remote Site Monitor jobs in Colorado? For Remote Site Monitor jobs in Colorado, the most frequently searched job titles are:
What job categories do people searching Remote Site Monitor jobs in Colorado look for? The top searched job categories for Remote Site Monitor jobs in Colorado are:
What cities in Colorado are hiring for Remote Site Monitor jobs? Cities in Colorado with the most Remote Site Monitor job openings:
Remote Site Monitor jobs near you
Infographic showing various Remote Site Monitor job openings in Colorado as of July 2026, with employment types broken down into 70% Full Time, and 30% Part Time. Highlights an 100% Remote job distribution, with an average salary of $54,485 per year, or $26.2 per hour.

Clinical Study Monitor-Animal Health

Clingroup

Fort Collins, CO • Remote

$33.25 - $45.25/hr

Full-time

Re-posted 22 days ago

Job description

Study Monitor - Clinaxel, United States of America

Clinaxel is part of a group of Animal Health Contract Research Organizations servicing the global animal health industry.


We're actively seeking aNorth American based Study Monitor to join our expanding Field Clinical Trials team. This role provides the flexibility to work remotely, with occasional office visits required to Waverly, New York and Fort Collins, Colorado.

Primary Job Purpose

Responsible for performing monitoring activities to ensure clinical trials are conducted in compliance with study protocols, VICH GL9 GCP guidelines, and applicable regulatory requirements. The role involves verifying data accuracy, ensuring site adherence to timelines and quality standards, and supporting the overall success of clinical trials.

Key responsibilities include serving as the primary contact for assigned study sites, training site staff on protocols and compliance, and identifying and addressing site-level issues. By maintaining high standards in monitoring practices, this role contributes to the integrity of clinical trial outcomes and advancement in animal health.

Job Specific Duties and Responsibilities

  • Conduct routine site monitoring visits across all trial phases to ensure compliance with study protocols, GCP guidelines, and regulatory requirements.
  • Verify the accuracy and completeness of data collected at study sites, identifying and resolving discrepancies as needed.
  • Serve as a point of contact for assigned study sites and investigators, facilitating communication and addressing site-level issues.
  • Assist in the preparation and review of study-related documentation, including monitoring reports and site records.
  • Provide guidance and support to site staff on study protocols, compliance requirements, and best practices.
  • Document and escalate risks or issues that may impact study timelines or data quality to the appropriate stakeholders.
  • Ensure site adherence to established timelines, quality standards, and budgetary constraints.
  • Maintain accurate and organized records within the study master file for assigned sites.
  • Collaborate with the team members to support smooth trial operations and successful study outcomes.
  • Promote adherence to organizational policies, ethical research practices, and regulatory standards at all times.
  • Provide guidance, technical support and training to Assistant Monitors, Monitor Associates, and peers where applicable.

Qualification, Training and Experience Requirements

  • Bachelor's degree in a relevant Life Sciences field.
  • Minimum of two years' experience in GCP study monitoring within Animal Health or Human Pharma sectors.
  • Solid understanding of clinical monitoring processes, including site initiation, routine monitoring visits, and close-out activities.
  • Familiarity with regulatory guidelines such as VICH GL9 GCP and their application in clinical trials.
  • Strong technical writing and oral presentation skills in English.
  • Competence in Electronic Data Capture Systems.
  • Demonstrated exceptional organizational and project management capabilities.

Important Note to Applicants

This is a remote position with potential for regular travel.

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The Company complies with local and international data protection and privacy legislation. This includes transparency in the processing of personal information processed about job applicants during the recruitment process. By applying for this position, applicants agree to the processing of their personal data in accordance with our recruitment procedure and Privacy Notice available from our website.

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