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Freelance Biotech Clinical Research Jobs (NOW HIRING)

Smarter HR Solutions LLC

NY · On-site

$90 - $100/hr

Senior Clinical Research Coordinator (CRC) Full time | Smarter HR Solutions LLC | United States Posted On 07/27/2026 Job Information Pharma/Biotech/Clinical Research Work Experience 4-5 years $90,000 ...

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ClinChoice

... biotechnology, medical device, and consumer health companies. We have over 28 years of proven high ... Senior Clinical Research Associate, Senior CRA, Freelance, Self-employed, Contract, Site Management ...

IQVIA

Clinical Research Associate, IQVIA Biotech

Ithaca, NY · On-site

$71K - $169K/yr

IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring and will also ... Job Overview We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play ...

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How much do freelance biotech clinical research jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for freelance biotech clinical research in the United States is $24.09, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $24.76 per hour, depending on experience, location, and employer.

What is the difference between Freelance Biotech Clinical Research vs Biotech Clinical Research Associate?

AspectFreelance Biotech Clinical ResearchBiotech Clinical Research Associate
CredentialsVaries; often requires industry experience, certifications optionalTypically requires a degree in life sciences and relevant certifications (e.g., CCR)
Work EnvironmentRemote or on-site, project-based, flexible schedulePrimarily on-site at clinical trial sites, structured hours
Employer & Industry UsageIndependent contractors, consulting firms, biotech companiesBiotech or pharmaceutical companies, CROs, research institutions

Freelance Biotech Clinical Researchers often work independently on specific projects with flexible hours, while Clinical Research Associates typically work full-time at trial sites or offices with structured schedules. Both roles require industry knowledge, but the freelance role offers more flexibility and varied work environments.

What cities are hiring for Freelance Biotech Clinical Research jobs?

Cities with the most Freelance Biotech Clinical Research job openings:

What are the most commonly searched types of Biotech Clinical Research jobs?

The most popular types of Biotech Clinical Research jobs are:

What states have the most Freelance Biotech Clinical Research jobs?

States with the most job openings for Freelance Biotech Clinical Research jobs include:

Freelance Biotech Clinical Research jobs near you

Senior Clinical Research Coordinator (CRC)

Smarter HR Solutions LLC

NY • On-site

$90 - $100/hr

Other

Medical, Dental, Vision

Posted yesterday

New

Job description

Senior Clinical Research Coordinator (CRC)

Full time | Smarter HR Solutions LLC | United States

Posted On 07/27/2026

Job Information

Pharma/Biotech/Clinical Research

Work Experience 4-5 years

$90,000-$100,000 per year

City Orange

State/Province California

92868

Job Description

***Please note: This position is onsite and not remote. Candidates must be based in the Orange, CA area, as relocation assistance is not provided. Only individuals authorized to work in the U.S. will be considered.***

Job Title: Senior Clinical Research Coordinator (Liver Trials)

Job Type: Full-Time | On-Site

Job Location: Orange, CA

Job Salary: $90,000-$100,000 per year (based on experience)

Industry: Clinical Research | Hepatology | Phase I-IV Trials

About Us

Join a fast-paced, compliance-driven research clinic specializing in liver disease trials—from NASH and cirrhosis to hepatocellular carcinoma. The clinic partners with leading sponsors and CROs to deliver high-quality, audit-ready data and compassionate patient care.

Position Overview

This is an on-site position in Orange, CA, and applicants must reside within a commutable distance of 50 miles or less or be able to independently relocate. THIS IS NOT A REMOTE POSITION.

We’re seeking a Senior Clinical Research Coordinator (CRC) with hands‑on experience in liver-focused clinical trials. You’ll lead study execution, regulatory coordination, and patient engagement across multiple protocols.

MUST HAVE - Experience in CRC in Liver/GI/Obesity studies

MUST HAVE - Regulatory experience

MUST HAVE - Fluency in Spanish

Key Responsibilities
  • Coordinate Phase I-IV liver trials, including screening, enrollment, and follow-up
  • Manage regulatory submissions (IRB, CPHS), source documentation, and AE reporting
  • Oversee biospecimen handling and lab coordination
  • Maintain CTMS and EDC systems (REDCap, Medidata, etc.)
  • Mentor junior CRCs and support cross-functional study teams
Requirements Qualifications
  • 3-5+ years of CRC experience in liver/hepatology trials
  • Strong knowledge of FDA, ICH-GCP, and HIPAA regulations
  • Proficiency in CTMS, EDC platforms, and protocol adherence
  • Excellent communication and documentation skills
  • Familiarity with California specific regulations
Certifications
  • CPHS Compliance Training (Required)
  • CCRC (Certified Clinical Research Coordinator) (Preferred)
  • Competitive salary + performance bonuses
  • Health, dental, and vision coverage
  • Paid training and certification support
  • Career growth in a high-impact research setting
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