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Overnight 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 ...

$52 - $70/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 ...

New

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

New

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

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Overnight Biotech Clinical Research information

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

As of Sep 4, 2026, the average hourly pay for overnight 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 Overnight Biotech Clinical Research vs Clinical Research Associate?

AspectOvernight Biotech Clinical ResearchClinical Research Associate
CredentialsTypically requires a bachelor's degree in life sciences or related fieldRequires a bachelor's degree, often with certification in clinical research
Work EnvironmentLaboratory settings, biotech companies, or clinical trial sites, often with flexible or overnight shiftsClinical trial sites, monitoring visits, and data management in healthcare or research facilities
Employer & IndustryBiotech firms, pharmaceutical companies, research organizationsPharmaceutical companies, CROs, healthcare institutions

Overnight Biotech Clinical Research roles focus on laboratory and biotech environments, often involving overnight shifts, while Clinical Research Associates primarily monitor clinical trials at sites. Both roles require similar educational backgrounds but differ in daily tasks and work settings.

What cities are hiring for Overnight Biotech Clinical Research jobs?

Cities with the most Overnight 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 Overnight Biotech Clinical Research jobs?

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

Senior Scientist, Clinical Research

Scorpion Therapeutics

South San Francisco, CA • On-site

$117 - $184/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 5 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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