1

Freelance Biotech Clinical Research Jobs (NOW HIRING)

Company Description M3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology ...

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Company Description M3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology ...

$60 - $80/hr

Company Description M3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology ...

Clinical Research Coordinator Prime Clinical Research Location: On-Site Employment Type: Full-Time ... companies, biotechnology organizations, and contract research organizations. Our mission is to ...

Clinical Research Coordinator

Jersey City, NJ · On-site

$25.25 - $33.75/hr

Required Qualifications Bachelor's or Master's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Microbiology, or a related field. 0-3 years of experience in clinical research or clinical ...

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Bachelor's or Master's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Microbiology, or a related field. * 0-3 years of experience in clinical research or clinical trial coordination.

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Required Qualifications Bachelor's or Master's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Microbiology, or a related field. 0-3 years of experience in clinical research or clinical ...

next page

Showing results 1-20

Freelance Biotech Clinical Research information

See salary details

$13

$24

$40

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

As of Sep 7, 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:

Senior Scientist, Clinical Research

Scorpion Therapeutics

South San Francisco, CA • On-site

$150 - $200/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 9 days ago


Job description

Early Clinical Scientist (ECS) coordinates the design, planning, and execution of early phase clinical trials with the Clinical Director and internal/external teams. Oversees trials within/across programs/therapeutic areas to ensure excellent execution and compliance supporting study objectives and data validity. Manages internal/external team performance, resolves performance issues, and ensures appropriate clinical safety assessment and risk management. Provides real-time oversight of ongoing trials to identify/mitigate patient, study design, data, or conduct issues; reviews and interprets clinical trial data. May conduct on-site monitoring, including site training and supervision of novel endpoint/biomarker collection. Applies GCP, ICH, and regulatory requirements.

Represents Early Stage Development on cross-functional teams; develops/improves job aids/SOPs/procedures and promotes best practices.

Technical writing: Co-authors protocols, investigator brochures, clinical study reports, WMA/CTD sections, safety reports, clinical development plans, publications, and abstracts; develops study operational documents.

Project management: Manages trial/program projects; meetings and document workspace management; risk assessment and contingency planning under accelerated timelines.

Education: Degree in Life Sciences; Bachelor’s +6 years, or Master’s +4 years, or PhD/doctorate +2 years (clinical trial management/execution; site training/monitoring; medical/regulatory writing).

Required: 3+ years operational clinical scientist/study manager in pharma/biotech; clinical research development process knowledge (program planning to regulatory submission); ability to learn therapeutic areas quickly; manage complex projects under accelerated timelines; scientific/medical/safety writing & reporting (at least one); partner with internal/external teams; collaboration/leadership/communication; GCP/ICH/regulatory knowledge.

Preferred: Global Phase I trials/safety reporting/WMA submission; Immunology and/or vaccine trial experience.

Salary range: $117,000.00–$184,200.00; annual bonus/long-term incentive if applicable.

  • Benefits include medical/dental/vision, 401(k), paid holidays, vacation, and sick/compassionate days.
#J-18808-Ljbffr