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Contract Biotech Clinical Research Jobs (NOW HIRING)

... biotechnology organizations, and contract research organizations. Our mission is to advance medical innovation while maintaining the highest standards of patient safety, regulatory compliance, and ...

$60 - $80/hr

Facilitates preparation and execution of contractual agreements with pharmaceutical, biotechnology ... Prior experience in clinical trials contract negotiation highly preferred * 3 years of research ...

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Coordinate with Principal Investigators, sponsors, Contract Research Organizations (CROs ... Bachelor's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Medicine, or a related health ...

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Coordinate with Principal Investigators, sponsors, Contract Research Organizations (CROs ... Bachelor's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Medicine, or a related health ...

Clinical Research Coordinator

Boston, MA · On-site

$26.25 - $35/hr

Coordinate with Principal Investigators, sponsors, Contract Research Organizations (CROs ... Bachelor's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Medicine, or a related health ...

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Coordinate with Principal Investigators, sponsors, Contract Research Organizations (CROs ... Bachelor's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Medicine, or a related health ...

Clinical Research Coordinator

Boston, MA · On-site

$26.25 - $35/hr

Coordinate with Principal Investigators, sponsors, Contract Research Organizations (CROs ... Bachelor's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Medicine, or a related health ...

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Contract Biotech Clinical Research information

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$12

$41

$69

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

As of Sep 8, 2026, the average hourly pay for contract biotech clinical research in the United States is $41.13, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $52.64 per hour, depending on experience, location, and employer.

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

AspectContract Biotech Clinical ResearchClinical Research Associate
CredentialsTypically requires a degree in life sciences, certifications like CCR or RAC beneficialRequires a degree in life sciences; certifications like CCR often preferred
Work EnvironmentContract-based, project-specific, often in biotech or pharmaceutical companiesUsually employed by CROs or sponsors, monitoring clinical trials at sites
Employer & IndustryBiotech firms, pharmaceutical companies, contract research organizationsPharmaceutical companies, CROs, biotech firms

Contract Biotech Clinical Research professionals focus on specific projects within biotech or pharma companies, often working on trial design and management. Clinical Research Associates primarily monitor clinical trials at sites, ensuring compliance and data integrity. While both roles require similar credentials and work in related environments, their responsibilities and employment types differ.

What cities are hiring for Contract Biotech Clinical Research jobs?

Cities with the most Contract 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 Contract Biotech Clinical Research jobs?

States with the most job openings for Contract 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.
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