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Overnight Biotech Clinical Research Jobs (NOW HIRING)

Winaxis

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.

Winaxis

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 ...

New

Winaxis

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 ...

IQVIA

Clinical Research Associate, IQVIA Biotech

Austin, TX · 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 ...

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 ...

IQVIA

Clinical Research Associate, IQVIA Biotech

Austin, TX · 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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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:

Overnight Biotech Clinical Research jobs near you

Senior Clinical Research Coordinator

Headlands Research

Riverside, CA

$25.25 - $33.75/hr

Full-time

Re-posted 5 days ago

Job description

 Riverside, CA
Artemis Institute for Clinical Research (a Headlands Research site)
 Full-time | Onsite (no opportunities for hybrid or remote)

For experienced CRCs looking for stability, collaboration, and meaningful work

If you're an experienced Clinical Research Coordinator who values strong operations, multidisciplinary collaboration, and a schedule that actually supports work-life balance, Artemis Institute for Clinical Research may be the right next step in your career.

Our Riverside site is known for its depth of experience, thoughtful study execution, and team-based approach to clinical research-particularly in vaccines, CNS, general medicine, and psychiatry.

About Artemis Institute for Clinical Research

Artemis Institute for Clinical Research in Riverside is a patient-centered clinical research site and part of the Headlands Research family. Founded with a core mission to prioritize patients, advance medicine, and improve the world, Artemis combines rigorous, process-driven trial management with a compassionate approach to care. The site conducts high-quality clinical trials across multiple therapeutic areas-including psychiatric, metabolic, vaccine, and healthy volunteer studies-and has helped thousands of participants contribute to meaningful medical advancements. Artemis is known for its collaborative team culture, strong operational standards, and commitment to excellence in delivering reliable, protocol-compliant research on behalf of pharmaceutical and biotech sponsors.

Why Experienced CRCs Choose Artemis
  • Multi-disciplinary collaboration with seasoned investigators and clinical staff
  • Strong operational support and clear SOPs
  • Exposure to complex, meaningful studies-not just high-volume turnover
  • Backing of a growing research network with resources and stability

This role is ideal for CRCs who enjoy owning their studies, working with competent teams, and being trusted to execute with precision.

Responsibilities:

  • Provide the highest level of care for study patients
  • Deliver excellent customer service to pharmaceutical clients
  • Coordinate all aspects of assigned clinical trials from site initiation through close-out
  • Conduct subject visits and ensure accurate, timely documentation in compliance with protocol and standards
  • Maintain compliance with protocols, GCP/ICH guidelines, FDA regulations, IRB requirements, and SOPs
  • Manage subject recruitment, informed consent, and retention activities
  • Ensure timely EDC data entry and resolution of queries
  • Report and follow up on AEs, SAEs, and protocol deviations
  • Collaborate with investigators, sponsors/CROs, labs, and internal teams
  • Prepare for and participate in monitoring visits, audits, and inspections
  • Maintain regulatory documentation and ensure training compliance for amendments and systems
  • Perform study procedures such as phlebotomy, ECGs, and sample processing (as trained)
  • Attend investigator meetings and provide cross-functional support as needed
  • Maintain working knowledge of protocols, lab manuals, equipment calibration, and inventory

Requirements:

  • At least two years of experience managing multiple phase 2-4 industry-sponsored clinical trial studies as the primary coordinator required
  • High school diploma or GED required
  • Strong understanding of FDA regulations, ICH-GCP, and clinical trial operations
  • Experience with EDC, IVRS, and clinical research platforms
  • Proficiency in medical terminology and clinical documentation
  • Strong organizational skills with the ability to manage multiple studies
  • Clear, professional verbal and written communication skills
  • Comfortable working onsite in a collaborative, clinical environment
Who Thrives in This Role
  • CRCs who want structure, support, and accountability
  • Those interested in taking the next step in managing people
  • Professionals who value teamwork over silos
  • Coordinators who care about data quality, patient experience, and compliance
  • Those ready to grow within a stable, well-established research site

 Apply today if you're looking for a CRC role where your experience is respected, your schedule is predictable, and your work directly contributes to advancing meaningful medical research.

Apply