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Work From Home Clinical Research Associate Jobs in Colorado

Senior Clinical Research Associate

Denver, CO ยท On-site +1

$110K - $138K/yr

... work and interact with each other, customers, patients and suppliers. The Sr. Clinical Research ... Experience collaborating with sites from initial engagement through close-out phases * Experience ...

Work from Home

Littleton, CO ยท Remote

$18/hr

We are excited to announce that currently we are looking for a 100% remote (work from home-WFH) ... clinical research services, commercial insights and healthcare intelligence to the life sciences ...

Work from Home

Fort Collins, CO ยท Remote

$18/hr

We are excited to announce that currently we are looking for a 100% remote (work from home-WFH) ... clinical research services, commercial insights and healthcare intelligence to the life sciences ...

We are excited to announce that currently we are looking for a 100% remote (work from home-WFH) ... clinical research services, commercial insights and healthcare intelligence to the life sciences ...

We are excited to announce that currently we are looking for a 100% remote (work from home-WFH) ... clinical research services, commercial insights and healthcare intelligence to the life sciences ...

Work from Home

Denver, CO ยท Remote

$18/hr

We are excited to announce that currently we are looking for a 100% remote (work from home-WFH) ... clinical research services, commercial insights and healthcare intelligence to the life sciences ...

Work from Home

Fort Collins, CO ยท Remote

$18/hr

We are excited to announce that currently we are looking for a 100% remote (work from home-WFH) ... clinical research services, commercial insights and healthcare intelligence to the life sciences ...

We are excited to announce that currently we are looking for a 100% remote (work from home-WFH) ... clinical research services, commercial insights and healthcare intelligence to the life sciences ...

Work from Home

Denver, CO ยท Remote

$18/hr

We are excited to announce that currently we are looking for a 100% remote (work from home-WFH) ... clinical research services, commercial insights and healthcare intelligence to the life sciences ...

WORK FROM HOME

Pueblo, CO ยท On-site +1

$300 - $500/wk

We are looking for individuals interested in working from home, remotely, as life insurance sales representatives. We are hiring coachable individuals comfortable with a 100% commission based income ...

... work effectively with clinical teams * Experience building research infrastructure in ambiguous, build-from-scratch environments -- you've stood something up without a playbook before This is not a ...

Remote Sales Work From Home

Denver, CO ยท On-site +1

$60K - $200K/yr

Remote Sales Work From Home Organization Description: There has never been a better time to have total control of your schedule with the ability to meet with clients remotely, over the phone, or in ...

Work From Home Remote Sales

Greeley, CO ยท On-site +1

$100K/yr

... IMO, offering a dynamic work environment where you can operate from your own location. Our ... homes, via Zoom, or over the phone Assist clients in applying for insurance policies Sell ...

... IMO, offering a dynamic work environment where you can operate from your own location. Our ... homes, via Zoom, or over the phone Assist clients in applying for insurance policies Sell ...

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Showing results 1-20

Work From Home Clinical Research Associate information

See Colorado salary details

$37.9K

$99.2K

$150.9K

How much do work from home clinical research associate jobs pay per year?

As of Sep 8, 2026, the average yearly pay for work from home clinical research associate in Colorado is $99,173.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,700.00 and $134,600.00 per year, depending on experience, location, and employer.

What does a work from home clinical research associate do?

A Work From Home Clinical Research Associate (CRA) is responsible for overseeing clinical trials and studies to ensure they are conducted according to protocols, regulatory requirements, and good clinical practice guidelines. Working remotely, CRAs monitor data collection, verify patient records, ensure compliance, and communicate with trial sites primarily through digital tools. They play a vital role in maintaining the integrity of research while providing flexibility to work from home.

What are the key skills and qualifications needed to thrive as a work from home clinical research associate?

To thrive as a Work From Home Clinical Research Associate, you need a solid background in life sciences, knowledge of clinical trial protocols, and typically a bachelor's degree in a related field. Familiarity with electronic data capture (EDC) systems, regulatory compliance tools, and Good Clinical Practice (GCP) certification are commonly required. Strong organizational skills, self-motivation, and effective remote communication set top performers apart in this role. These skills ensure accurate trial monitoring, regulatory adherence, and seamless collaboration despite the remote work environment.

How does remote work impact the collaboration and communication of a work from home clinical research associate with site staff and sponsors?

As a Work From Home Clinical Research Associate, effective collaboration and communication with site staff and sponsors are primarily managed through virtual meetings, emails, and specialized clinical trial management software. While remote work offers flexibility, it also requires proactive communication to ensure timely monitoring, issue resolution, and adherence to study timelines. Building strong relationships remotely can be challenging, but leveraging technology, maintaining regular check-ins, and being responsive help foster trust and smooth collaboration. It's important to stay organized and document all interactions thoroughly for regulatory compliance and project continuity.

What is the difference between Work From Home Clinical Research Associate vs Clinical Trial Coordinator?

AspectWork From Home Clinical Research AssociateClinical Trial Coordinator
CertificationsTypically requires CRA certification or equivalentOften requires certification or relevant experience
Work EnvironmentPrimarily remote, overseeing multiple sites remotelyUsually on-site or hybrid, managing trial logistics
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research centers, clinical sites

Work From Home Clinical Research Associates focus on monitoring clinical trials remotely, ensuring compliance and data integrity, often working for CROs or pharma companies. Clinical Trial Coordinators handle the day-to-day operations at trial sites, coordinating activities and participant management. Both roles require knowledge of clinical protocols but differ mainly in work setting and responsibilities.

What are the most commonly searched types of Work From Home Clinical Research jobs in Colorado?

The most popular types of Work From Home Clinical Research jobs in Colorado are:

What are popular job titles related to Work From Home Clinical Research Associate jobs in Colorado?

For Work From Home Clinical Research Associate jobs in Colorado, the most frequently searched job titles are:

What job categories do people searching Work From Home Clinical Research Associate jobs in Colorado look for?

The top searched job categories for Work From Home Clinical Research Associate jobs in Colorado are:

What cities in Colorado are hiring for Work From Home Clinical Research Associate jobs?

Cities in Colorado with the most Work From Home Clinical Research Associate job openings:

Infographic showing various Work From Home Clinical Research Associate job openings in Colorado as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, and 4% Contract. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $99,173 per year, or $47.7 per hour.

Senior Clinical Research Associate

ICON

Denver, CO โ€ข On-site, Remote

$110K - $138K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 27 days ago


Job description

Senior Clinical Research Associate - Oncology Phase I - Denver, CO
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
The Sr. Clinical Research Associate (Sr. CRA) will be responsible for performing investigative site management and monitoring activities throughout the clinical trial lifecycle. This Sr. CRA role will support the client's Oncology clinical trials to ensure data integrity, subject safety, and inspection readiness at the clinical investigative sites.
Responsibilities:
  • Perform site management activities to support the client's Oncology site success and maintain a continuous state of inspection readiness
  • Act as the primary contact and facilitate efficient communications between the client's clinical trial team and the sites
  • Perform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits and Close-Out Visits) to ensure data integrity and subject safety in the client's trials
  • May perform oversight activities to assess monitoring quality and train/mentor less experienced CRAs
  • Promptly document monitoring activities and submit/approve visit reports
  • Manage site essential document collection and TMF reconciliation with site files
  • Support sites with local Institutional Review Board (IRB)/Ethics Committee (EC) submissions and confirm approvals
  • Regularly review site Key Risk Indicator (KRI) metrics, issues and action items to detect trends and ensure prompt resolution
  • Independently determine root causes and develop/implement site Corrective Action and Preventive Action (CAPA) plans
  • Deliver training to ensure sites comply with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs) and regulations
  • Support sites and the client's regulatory inspections
  • Contribute to site identification; drive site feasibility and qualification progress; and support site activation activities
  • Lead site engagement initiatives and foster relationships with key Oncology sites and networks

Qualifications
  • Bachelor's degree (scientific field preferred)
  • 5+ years monitoring clinical trials independently conducting on-site and remote monitoring visits. Atleast 2 years monitoring solid tumor clinical trials.
  • 1+ years early development oncology trial experience and/or Phase III Oncology trial experience
  • Solid tumor clinical trial experience is required
  • Experience utilizing Veeva systems is highly preferred
  • Demonstrated experience developing/maintaining site relationships and securing compliance
  • Expertise in GxPs and Oncology monitoring techniques (including Risk-Based Monitoring) and terminology
  • Experience collaborating with sites from initial engagement through close-out phases
  • Experience activating sites
  • Experience training site staff
  • Experience supporting sites and/or sponsors in regulatory inspections
  • Experience working within a Functional Services (or in-house) monitoring model is preferred
  • Willing to travel up to 50%

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Salary Range
$110,520.00-$138,150.00
Are you a current ICON Employee? Please click here to apply