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Remote Clinical Trial Associate Jobs in Colorado

CPC

Drug Supply/Clinical Trial Supply Manager

Aurora, CO · Remote

$70K - $90K/yr

We are looking for a Drug Supply/Clinical Trial Supply Manager to join our team! Responsible for ... Flexible and remote work schedules An Equal Opportunity Employer CPC provides equal employment ...

ICON

Senior Clinical Research Associate

Denver, CO · On-site +1

$110K - $138K/yr

Senior Clinical Research Associate - Oncology Phase I - Denver, CO ICON is a global healthcare ... trial team and the sites * Perform remote and on-site monitoring/co-monitoring visits (Site ...

CPC

Clinical Operations Manager II

Aurora, CO · Remote

$71K - $88K/yr

Remote candidates are welcome to apply. In this position you will: * Oversee clinical operations ... Oversee trial-related activities. * Track and approve vendor payments. * Provide expert advice in ...

CPC

Sr. Clinical Operations Manager

Aurora, CO · On-site +1

Remote candidates are welcome to apply. General Responsibilities: * Work closely with the Head of ... Oversee trial-related activities and provide performance feedback to supervisors for all project ...

micro1 AI

Director of Biostatistics

Thornton, CO · Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... clinical trial analysis, regulatory submission reviews, and observational study assessments.

micro1 AI

Director of Biostatistics

Westminster, CO · Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... clinical trial analysis, regulatory submission reviews, and observational study assessments.

micro1 AI

Biostatistician

Longmont, CO · Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... clinical trial analysis, regulatory submission reviews, and observational study assessments.

micro1 AI

Biostatistician

Thornton, CO · Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... clinical trial analysis, regulatory submission reviews, and observational study assessments.

micro1 AI

Director of Biostatistics

Centennial, CO · Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... clinical trial analysis, regulatory submission reviews, and observational study assessments.

micro1 AI

Biostatistician

Centennial, CO · Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... clinical trial analysis, regulatory submission reviews, and observational study assessments.

micro1 AI

Director of Biostatistics

Arvada, CO · Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... clinical trial analysis, regulatory submission reviews, and observational study assessments.

micro1 AI

Director of Biostatistics

Aurora, CO · Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... clinical trial analysis, regulatory submission reviews, and observational study assessments.

micro1 AI

Director of Biostatistics

Lakewood, CO · Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... clinical trial analysis, regulatory submission reviews, and observational study assessments.

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All JobsClinical Trial Associate JobsRemote Clinical Trial Associate JobsRemote Clinical Trial Associate Jobs in Colorado

Remote Clinical Trial Associate information

See Colorado salary details

$18

$42

$73

How much do remote clinical trial associate jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for remote clinical trial associate in Colorado is $42.05, according to ZipRecruiter salary data. Most workers in this role earn between $33.89 and $46.25 per hour, depending on experience, location, and employer.

What does a remote clinical trial associate do?

A Remote Clinical Trial Associate (CTA) supports the planning, execution, and management of clinical trials from a remote location. Their responsibilities include handling documentation, assisting with regulatory submissions, maintaining trial records, and coordinating communication between trial sites, sponsors, and regulatory bodies. Remote CTAs play a crucial role in ensuring that trials are conducted according to protocols, timelines, and regulatory requirements, all while working offsite. This allows for greater flexibility and can improve efficiency in clinical research processes.

What are the key skills and qualifications needed to thrive as a remote clinical trial associate, and why are they important?

To thrive as a Remote Clinical Trial Associate, you need a solid understanding of clinical research processes, regulatory guidelines, and typically a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and Good Clinical Practice (GCP) certification are commonly required. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for managing study documentation and collaborating with remote teams. These competencies ensure trials are conducted efficiently, compliantly, and with high data integrity in a virtual environment.

What are some common challenges faced by remote clinical trial associates, and how can they be managed?

Remote Clinical Trial Associates often encounter challenges such as maintaining consistent communication with on-site teams, managing multiple studies across different time zones, and ensuring accurate documentation while working virtually. These can be managed by leveraging robust digital communication tools, setting clear expectations for updates, and staying organized with project management software. Proactively building relationships with colleagues and participating in regular virtual meetings also helps ensure alignment and smooth coordination throughout the trial process.

What are the most commonly searched types of Remote Clinical Trial jobs in Colorado?

The most popular types of Remote Clinical Trial jobs in Colorado are:

What are popular job titles related to Remote Clinical Trial Associate jobs in Colorado?

For Remote Clinical Trial Associate jobs in Colorado, the most frequently searched job titles are:

What job categories do people searching Remote Clinical Trial Associate jobs in Colorado look for?

The top searched job categories for Remote Clinical Trial Associate jobs in Colorado are:

Remote Clinical Trial Associate jobs near you
Infographic showing various Remote Clinical Trial Associate job openings in Colorado as of August 2026, with employment types broken down into 2% As Needed, 75% Full Time, 17% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $87,454 per year, or $42 per hour.

Clinical Study Monitor-Animal Health

Clingroup

Fort Collins, CO • Remote

$33.25 - $45.25/hr

Full-time

Re-posted 27 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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