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Freelance Labcorp Clinical Trials Jobs (NOW HIRING)

Solomon Page

Contract CRC - Dermatology

White Plains, NY · On-site

$40 - $45/hr

... dermatological clinical trials. * Coordinating study visits, administering study treatments ... freelancers - which sets us apart in the industries we serve. About Solomon Page Founded in 1990 ...

Solomon Page

Sr. CRA - Direct Hire

Manhattan, NY · On-site

$105/hr

Experience monitoring clinical trials PI-IV. * Strong knowledge of clinical research regulations ... freelancers - which sets us apart in the industries we serve. About Solomon Page Founded in 1990 ...

ClinChoice

Senior Clinical Research Associate, Senior CRA, Freelance, Self-employed, Contract, Site Management, Monitor, Monitoring, Complex Trials, Medical Devices, Cardiology, Neurology, Open to Travel ...

Solomon Page

CRA - Alberta, Canada

Manhattan, NY · On-site

$80 - $90/hr

Experience monitoring clinical trials PI-IV. * Strong knowledge of clinical research regulations ... freelancers - which sets us apart in the industries we serve. About Solomon Page Founded in 1990 ...

N Side

Director of Strategic Growth

Cambridge, MA · On-site

... hundreds of clinical trials around the world. Which leads to waste reduction, faster ... Contract : Freelance We are looking forward to receiving your application! We are committed to ...

LILT, Inc

$39K - $51K/yr

Life Sciences, Medical, Clinical trials, etc. Please note that this is a remote, freelance contractor position. Requirements * Native or fluent in the target language (reading and writing)

Solomon Page

Sr CTA - Autoimmune

San Diego, CA · On-site

$35 - $48/hr

The Senior Clinical Trial Associate supports the operational execution of clinical studies by ... to help ensure trials are conducted in compliance with applicable regulations and company ...

NCH

Lab Asst Phleb Patient Reg Fam Med

Naples, FL · On-site

$19.25 - $25.25/hr

Conduct research and participate in national clinical trials; and partner with other health market ... NCH, LabCorp or QUEST). Recognizes specimens and tests which must be prioritized due to specimen ...

Everyday Health - Professional

You will conduct literature reviews of clinical trials, peer-reviewed articles, clinical guidelines ... Review content developed by other medical writers and freelancers, and provide guidance and/or ...

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Freelance Labcorp Clinical Trials information

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How much do freelance labcorp clinical trials jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for freelance labcorp clinical trials in the United States is $47.71, according to ZipRecruiter salary data. Most workers in this role earn between $24.28 and $61.78 per hour, depending on experience, location, and employer.

How do freelance professionals typically collaborate with Labcorp clinical trials teams, and what can applicants expect in terms of communication and workflow?

Freelance professionals working with Labcorp clinical trials often collaborate remotely with multidisciplinary teams, including clinical research associates, project managers, and data analysts. Communication is typically managed through regular virtual meetings, email updates, and project management platforms to ensure alignment on study protocols and timelines. Freelancers can expect a structured workflow with clearly defined deliverables, regular feedback, and the opportunity to contribute their expertise to various phases of the clinical trial process. Building strong communication skills and adaptability is key, as projects may evolve rapidly based on regulatory requirements or study outcomes.

What is a freelance Labcorp clinical trials professional?

Freelance Labcorp Clinical Trials refer to research studies conducted by Labcorp, a global life sciences company, that engage independent professionals on a contract or freelance basis. These trials are designed to test new medications, medical devices, or treatments to ensure their safety and effectiveness. Freelancers may be involved in various roles, such as clinical research coordinators, data managers, or study recruiters, and can work remotely or on-site, depending on the project's needs. Participating in these trials can provide valuable experience in the clinical research field and opportunities to contribute to medical advancements.

What are the key skills and qualifications needed to thrive as a freelance Labcorp clinical trials professional?

To thrive as a Freelance Labcorp Clinical Trials professional, you need a solid background in clinical research, knowledge of trial protocols, and often a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications such as GCP (Good Clinical Practice) are typically required. Exceptional attention to detail, effective communication, and strong organizational skills help you excel in managing study documentation and collaborating with research teams. These competencies ensure trial integrity, regulatory compliance, and successful execution of clinical studies.
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Freelance Labcorp Clinical Trials jobs near you
Infographic showing various Freelance Labcorp Clinical Trials job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $99,230 per year, or $47.7 per hour.

Contract CRC - Dermatology

Solomon Page

White Plains, NY • On-site

$40 - $45/hr

Contractor

Medical, Dental, Retirement

Posted 6 days ago

Job description

Our client is seeking a Clinical Research Coordinator (CRC) for a contract-to-permanent opportunity.
  • Pay Range: $40-45/hour
  • Location: Westchester County, NY
Responsibilities:
  • Recruiting, pre-screening, and obtaining informed consent from patients participating in dermatological clinical trials.
  • Coordinating study visits, administering study treatments, performing clinical assessments, capturing clinical photography, and collecting and processing laboratory specimens.
  • Monitor and report adverse events and ensure accurate and timely documentation throughout the study.
  • Maintaining regulatory binders, preparing and submitting IRB documentation, and entering and managing clinical data within Electronic Data Capture (EDC) systems.
Required Qualifications:
  • Education: Bachelor's degree in a life science or healthcare field.
  • Experience: 3+ years of clinical research coordination, ideally with dermatology focus
  • Certifications: CCRC (Certified Clinical Research Coordinator) is a plus

If you meet the required qualifications and are interested in this role, please apply today.
The Solomon Page Distinction
Solomon Page offers a comprehensive benefit program for hourly employees. We pride ourselves on offering medical, dental, 401(k), direct deposit and commuter benefits to our employees, including freelancers - which sets us apart in the industries we serve.
About Solomon Page
Founded in 1990, Solomon Page is a specialty niche provider of staffing and executive search solutions across a wide array of functions and industries. The success of Solomon Page reflects an organic growth strategy supported by a highly entrepreneurial culture. Acting as a strategic partner to our clients and candidates, we focus on providing customized solutions and building long-term relationships based on trust, respect, and the consistent delivery of excellent results. For more information and additional opportunities, visit: solomonpage.com and connect with us on Facebook , and LinkedIn .
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