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Clinical Study Associate Jobs in Colorado (NOW HIRING)

The US Oncology Network

Study Coordinator

Denver, CO · On-site

$60K - $75K/yr

... Research Study Coordinator in Denver Bring your established interventional trials research ... clinical research Qualifications Education: * Associate's degree required, bachelor's degree ...

The US Oncology Network

Study Coordinator

Denver, CO

$60K - $75K/yr

Creates study specific tools for source documentation as well as checklists and clinic information ... clinical research Qualifications Education: * Associate's degree required, bachelor's degree ...

PSI CRO

Site Relationship Associate

Model, CO · Hybrid

$34K - $43K/yr

We understand what clinical study sites need, and our mission is to strengthen study delivery by ... As a Site Relations Associate , you will play a key role in expanding and strengthening Milestone ...

Milestone One

Site Relationship Associate

Model, CO · Hybrid

$34K - $43K/yr

We understand what clinical study sites need, and our mission is to strengthen study delivery by ... As a Site Relations Associate , you will play a key role in expanding and strengthening Milestone ...

Merck & Co.

Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor ... Associate's degree, certificate or equivalent in a scientific / healthcare discipline together with ...

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Clinical Study Associate information

See Colorado salary details

$13

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How much do clinical study associate jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for clinical study associate in Colorado is $33.16, according to ZipRecruiter salary data. Most workers in this role earn between $22.26 and $43.75 per hour, depending on experience, location, and employer.

What is a clinical study associate?

Clinical Study Associates (CSAs) are professionals who support the planning, execution, and monitoring of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They help coordinate study logistics, maintain study documentation, and ensure compliance with regulatory requirements. CSAs often work closely with Clinical Research Associates, study coordinators, and investigators to ensure that trials are conducted according to protocol and timelines. Their role is essential in ensuring the accuracy and integrity of data collected during clinical research.

What are some common challenges clinical study associates face when managing multiple clinical trials simultaneously?

Clinical Study Associates often juggle several clinical trials at once, which can present challenges such as prioritizing competing deadlines, maintaining accurate documentation for each study, and ensuring consistent communication with cross-functional teams. Staying organized and proactive is essential, as unforeseen protocol amendments or site issues can arise. Building strong relationships with site staff and utilizing effective project management tools can help CSAs navigate these complexities and deliver high-quality results.

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

To thrive as a Clinical Study Associate, you need a strong understanding of clinical research processes, regulatory requirements, and typically a life sciences degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are commonly required. Attention to detail, organizational skills, and effective communication set top performers apart in this role. These competencies ensure accurate study documentation, regulatory compliance, and smooth coordination across research teams.

What is the difference between Clinical Study Associate vs Clinical Research Coordinator?

AspectClinical Study AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like CCRP or CCRA beneficialBachelor's degree in health sciences or related field; certifications like CCRP advantageous
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospitals, clinics, research centers
Job FocusMonitoring clinical trials, ensuring protocol compliance, data accuracyManaging daily trial activities, patient recruitment, data collection
Employer & Industry UsageCommonly employed in pharma and CROsPrimarily in healthcare and academic research settings

Both roles involve clinical trial oversight but differ in focus: Clinical Study Associates primarily monitor and ensure compliance during trials, while Clinical Research Coordinators manage daily trial operations and patient interactions. Understanding these distinctions helps in choosing the right career path or job search focus.

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

The most popular types of Clinical Study jobs in Colorado are:

What cities in Colorado are hiring for Clinical Study Associate jobs?

Cities in Colorado with the most Clinical Study Associate job openings:

Clinical Study Associate jobs near you
Infographic showing various Clinical Study 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 $68,983 per year, or $33.2 per hour.

Clinical Study Monitor-Animal Health

Clingroup

Fort Collins, CO • Remote

$33.25 - $45.25/hr

Full-time

Re-posted 8 hours 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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