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Freelance Clinical Research Associate Jobs in Park Ridge, IL

ICON

Senior Clinical Research Associate

Chicago, IL · On-site +1

$110K - $138K/yr

Senior Clinical Research Associate - Oncology Phase I - Chicago ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments ...

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Senior Clinical Research Associate

Chicago, IL · Hybrid

$110K - $138K/yr

Senior Clinical Research Associate - Oncology Phase I - Chicago ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments ...

Icon plc

Clinical Research Associate

Chicago, IL · On-site

Clinical Research Associate 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 ...

Icon plc

Senior Clinical Research Associate

Chicago, IL · On-site

$110K - $138K/yr

Senior Clinical Research Associate - Oncology - Midwest ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

ICON

Senior Clinical Research Associate

Chicago, IL · On-site +1

$110K - $138K/yr

Senior Clinical Research Associate - Oncology - Midwest ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

Icon plc

Clinical Research Associate 2

Chicago, IL · On-site

$91K - $114K/yr

Clinical Research Associate- Mid-West 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 ...

ICON

Clinical Research Associate 2

Chicago, IL · On-site +1

$91K - $114K/yr

Clinical Research Associate- Mid-West 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 ...

Actalent

Clinical Research Coordinator

Lisle, IL · On-site

$24 - $31.75/hr

Research Coordinator The Research Coordinator supports clinical research studies by assisting investigators, research associates, and project managers with the day-to-day operations of study ...

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Clinical Research Associate II

Chicago, IL · On-site

$91K - $114K/yr

Clinical Research Associate - Oncology - Chicago ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

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Freelance Clinical Research Associate information

See Park Ridge, IL salary details

$35.4K

$92.8K

$141.2K

How much do freelance clinical research associate jobs pay per year?

As of Aug 27, 2026, the average yearly pay for freelance clinical research associate in Park Ridge, IL is $92,806.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,500.00 and $126,000.00 per year, depending on experience, location, and employer.

What is a freelance clinical research associate?

A Freelance Clinical Research Associate (CRA) is an independent professional who monitors clinical trials to ensure compliance with regulatory guidelines, protocols, and Good Clinical Practice (GCP). Unlike full-time CRAs, freelancers work on a contract basis for multiple sponsors, contract research organizations (CROs), or clinical sites. Their responsibilities include site visits, data verification, risk assessment, and communication with investigators. This role offers flexibility, diverse project opportunities, and control over workload but requires strong self-management and networking skills.

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

To thrive as a Freelance Clinical Research Associate, you need a strong background in clinical research, understanding of ICH-GCP guidelines, and typically a relevant life sciences degree. Familiarity with electronic data capture (EDC) systems, trial management software, and certifications such as GCP training are commonly expected. Excellent organizational skills, self-motivation, and clear communication are essential soft skills for managing independent workloads and liaising with multiple stakeholders. These abilities ensure regulatory compliance, accurate data collection, and successful coordination of clinical trials across diverse settings.

What are the typical challenges faced by freelance clinical research associates, and how can they be managed?

As a freelance Clinical Research Associate, you'll often manage multiple studies or sites at once, requiring strong time management and organizational skills. Challenges can include juggling different sponsor requirements, keeping up with regulatory changes, and maintaining clear communication across virtual teams. Effective use of project management tools, regular updates with stakeholders, and continuous professional development help address these challenges. Freelancers often enjoy greater flexibility but must proactively seek new contracts and networking opportunities to maintain steady work. Being adaptable and detail-oriented are key traits to thrive in this dynamic environment.

What are the most commonly searched types of Freelance Clinical Research jobs in Park Ridge, IL?

The most popular types of Freelance Clinical Research jobs in Park Ridge, IL are:

What job categories do people searching Freelance Clinical Research Associate jobs in Park Ridge, IL look for?

The top searched job categories for Freelance Clinical Research Associate jobs in Park Ridge, IL are:

What cities near Park Ridge, IL are hiring for Freelance Clinical Research Associate jobs?

Cities near Park Ridge, IL with the most Freelance Clinical Research Associate job openings:

Freelance Clinical Research Associate jobs near you
Infographic showing various Freelance Clinical Research Associate job openings in Park Ridge, IL as of August 2026, with employment types broken down into 2% As Needed, 72% Full Time, 19% Part Time, 6% Contract, and 1% Nights. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $92,806 per year, or $44.6 per hour.

Clinical Research Associate

Medasource

North Chicago, IL • On-site

Other

Posted 15 days ago

Job description

Title: Clinical Research Associate

Duration: 1 year contract (potential of extension)

Location: Remote with up to 75% travel


Job Description:

Abbott's Core Diagnostics team is seeking a Clinical Research Associate to support a Traumatic Brain Injury (TBI) clinical research initiative. This individual will support multi-site clinical trial operations while ensuring strict compliance with protocol in a highly regulated environment. The ideal candidate brings strong monitoring fundamentals, exceptional attention to detail, and the ability to operate independently across multiple sites and stakeholders.


Responsibilities:

  • Perform site qualification, initiation, interim monitoring, and close-out visits across assigned clinical sites
  • Support oversight of approximately 4-5 clinical research sites, including primary and secondary site responsibilities
  • Ensure protocol compliance, GCP adherence, and accurate study documentation
  • Conduct source data verification/review and investigational product accountability activities
  • Identify, document, and escalate site issues, deviations, and risks appropriately
  • Complete detailed trip reports, monitoring documentation, and required reporting within established timelines
  • Collaborate cross-functionally with clinical operations, investigators, and study coordinators
  • Support multiple studies simultaneously as needed
  • Maintain compliance with time tracking, reporting, and data handling procedures

Qualifications:

  • 3-5+ years of clinical research experience preferred
  • Open to candidates with:
  • CRA experience within sponsor environments
  • Strong clinical research coordinator experience from hospital or academic settings
  • Strong understanding of:
  • Site monitoring activities
  • Source data verification/review
  • Investigational product accountability
  • GCP and clinical trial documentation requirements
  • Excellent written and verbal communication skills
  • Strong critical thinking and situational problem-solving abilities
  • Ability to work independently and manage competing priorities across multiple sites
  • Highly organized with strong time management skills
  • Ability to travel nationally up to 75% as required
  • Comfortable operating within a 40-hour work week structure


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