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Overnight Clinical Research Organization Jobs (NOW HIRING)

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Overnight Clinical Research Organization information

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$49K

$107.3K

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How much do overnight clinical research organization jobs pay per year?

As of Sep 8, 2026, the average yearly pay for overnight clinical research organization in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What is an overnight clinical research organization?

An Overnight Clinical Research Organization (CRO) is a specialized company that provides support to pharmaceutical, biotechnology, and medical device industries by conducting clinical trials and research studies during overnight hours. These organizations often manage overnight inpatient studies where participants are monitored for safety and data collection throughout the night. This setup is crucial for trials that require continuous observation or specific dosing schedules that occur outside regular business hours. Overnight CROs ensure studies are conducted according to regulatory standards and provide critical data for the development of new treatments.

What are some unique challenges faced by professionals working overnight in a clinical research organization?

Overnight professionals in a Clinical Research Organization often face challenges such as maintaining alertness during extended or unconventional hours, coordinating effectively with daytime teams, and ensuring data integrity across shifts. Communication is key, as overnight staff must provide thorough handovers to daytime colleagues and may need to address urgent issues with limited on-site support. Additionally, balancing personal health and work-life needs can be more demanding, but many CROs offer resources and flexible scheduling to help staff adapt.

What are the key skills and qualifications needed to thrive as an overnight clinical research associate, and why are they important?

To thrive as an Overnight Clinical Research Associate, you need a solid background in life sciences or healthcare, knowledge of clinical trial protocols, and often a bachelor's degree in a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is typically required. Detail orientation, effective communication, and the ability to work independently during non-standard hours are valuable soft skills in this role. These skills ensure regulatory compliance, accurate data collection, and smooth trial operations while working outside traditional business hours.

What is the difference between Overnight Clinical Research Organization vs Clinical Research Coordinator?

AspectOvernight Clinical Research OrganizationClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are commonUsually requires a bachelor's degree; certifications like CCRP or CRC are advantageous
Work EnvironmentOperates mainly in clinical research facilities, hospitals, or labs, often with overnight shiftsWorks primarily in hospitals, clinics, or research sites during daytime hours
Employer & Industry UsageUsed by clinical research organizations conducting trials, often with 24/7 operationsEmployed by hospitals, research sites, or CROs to coordinate trials and patient visits

While both roles involve clinical research, Overnight Clinical Research Organizations focus on managing and supporting trials during overnight hours, often within specialized facilities. Clinical Research Coordinators handle day-to-day trial activities, patient coordination, and data collection during regular hours. Understanding these differences helps in choosing the right career path or job search focus.

What cities are hiring for Overnight Clinical Research Organization jobs?

Cities with the most Overnight Clinical Research Organization job openings:

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

The most popular types of Clinical Research Organization jobs are:

What states have the most Overnight Clinical Research Organization jobs?

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

Clinical Research Nurse (FT Overnights)

Celerion

Lincoln, NE • On-site

Other

Posted 10 days ago


Celerion rating

7.0

Company rating: 7.0 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

64th of 75 rated research


Job description

Full-time Overnight Clinical Research Nurse

Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.

Celerion is seeking a Full-time overnight Clinical Research Nurse to assist with our clinical research trials. This is a dynamic role working with a healthy population offering the ability to learn about clinical research and see the drug development process at work.

Are you looking for an opportunity that will make a difference in the future of health care? If so, we can't wait to meet you. Do you want to learn more?

Responsibilities

  • Perform scheduled events according to the study protocol.
  • Work directly with study managers to ensure a successful trial.
  • Work with participants in the research process, doing vital sign checks, ECGs, blood draws, and telemetry monitoring.
  • Identify and report adverse events to assist in the clinical research process.

Qualifications

  • Current NE RN or LPN license and clinical assessment skills.
  • ACLS certification is a plus.
  • Strong computer and documentation skills.

Shift:

You should be available to work the following scheduling availability:

Mon-Sun from 7p-7:30a. Clock in between 7p-9p. One weekend (Saturday and Sunday) a month. Shifts can be 5x8 or 4 x10 based on employee preference.

Celerion Values: Integrity Trust Teamwork Respect.

Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.

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