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Overnight Clinical Research Jobs (NOW HIRING)

How This Role Makes a Difference The Clinical Research Assistant is an entry level clinical ... Overnight travel will be minimal ( * Physical demands associated with this position Include : The ...

How This Role Makes a Difference The Clinical Research Assistant is an entry level clinical ... Overnight travel will be minimal ( * Physical demands associated with this position Include : The ...

Overnight travel may be required for training and/or investigative meetings. CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without ...

Clinical Research Coordinator 1

Pennington, NJ · On-site

$24.50 - $32.50/hr

Ability and willingness to travel extensively throughout Louisiana, including occasional overnight ... e.g., REDCap), clinical trial management systems, or other research databases. Pennington ...

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Overnight Clinical Research information

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$49K

$107.3K

$189K

How much do overnight clinical research jobs pay per year?

As of Aug 30, 2026, the average yearly pay for overnight clinical research 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 job?

Overnight clinical research jobs involve working non-traditional hours, typically overnight shifts, to oversee clinical trials or studies that require 24/7 monitoring of participants. Employees in these roles may collect data, monitor patient safety, administer medications, and ensure compliance with study protocols during nighttime hours. These positions are crucial for studies where continuous observation is necessary, such as sleep research or trials involving inpatient monitoring.

What are the key skills and qualifications needed to thrive as an overnight clinical research professional?

To thrive as an Overnight Clinical Research professional, you need a background in life sciences or nursing, experience in clinical trial protocols, and often a relevant degree or certification such as GCP (Good Clinical Practice). Familiarity with data collection software, electronic data capture (EDC) systems, and basic laboratory equipment is typically necessary. Attention to detail, strong organizational skills, and the ability to communicate clearly are valuable soft skills for this role. These competencies ensure accurate data collection, adherence to regulatory standards, and effective teamwork during late or overnight shifts critical to research integrity.

What are the unique challenges of working overnight shifts in clinical research, and how can professionals manage them?

Overnight shifts in clinical research often require adapting to non-traditional hours while maintaining high attention to detail and protocol compliance. Common challenges include managing fatigue, coordinating with day-shift team members, and ensuring effective communication across shift changes. Professionals can manage these by establishing a consistent sleep routine, leveraging handover tools, and participating in regular team meetings. Working overnight can also offer valuable experience with independently handling study procedures and troubleshooting issues, which can be advantageous for career growth.

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

AspectOvernight Clinical ResearchClinical Research Coordinator
CredentialsTypically requires a background in healthcare or life sciences, sometimes with certifications like CCRCRequires similar credentials, often with clinical research certifications or degrees in health sciences
Work EnvironmentConducts research activities during overnight hours, often in clinical settings or labsWorks during daytime hours in hospitals, clinics, or research facilities
Employer & Industry UsageFound in clinical trial sites, hospitals, and research institutionsEmployed by research organizations, hospitals, and pharmaceutical companies
Common Search & ComparisonOften compared due to scheduling differences and similar roles in clinical trials

Overnight Clinical Research involves conducting clinical trial activities during overnight shifts, focusing on data collection and patient monitoring. Clinical Research Coordinators typically work during regular hours, managing trial logistics and patient recruitment. Both roles require similar credentials and are integral to clinical trials, but differ mainly in work hours and specific responsibilities.

What cities are hiring for Overnight Clinical Research jobs?

Cities with the most Overnight Clinical Research job openings:

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

The most popular types of Clinical Research jobs are:

What states have the most Overnight Clinical Research jobs?

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

Infographic showing various Overnight Clinical Research job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Clinical Research Nurse (FT Overnights)

Lincoln, NE


Celerion
Pharmaceutical and Medicine Manufacturing • 1 - 5K employees

7.0

Company rating: 7.0 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

63rd of 74 rated research

People enjoy working here

Recommended by parents

Respectful managers


Full-time

Posted 2 days ago

New


Job description

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
  • You will be responsible for performing scheduled events according to the study protocol.
  • You will work directly with study managers to successfully ensure a successful trial.
  • You will work with participants in the research process, under our care, doing vital sign checks, ECGs, blood draws and telemetry monitoring.
  • You will also identify and report adverse events to assist in the clinical research process.
Qualifications
  • You will have a current NE RN or LPN license and clinical assessment skills
  • Your 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.
 

Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as "Not Junk" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.



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