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Overnight Clinical Research Jobs (NOW HIRING)

With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring ... Overnight travel will be minimal ( * Physical demands associated with this position Include : The ...

With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring ... Overnight travel will be minimal ( * Physical demands associated with this position Include : The ...

With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring ... Overnight travel will be minimal ( * Physical demands associated with this position Include : The ...

With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring ... 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 ...

Clinical Research Assistant

Mesa, AZ · On-site

$19 - $33/hr

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 ...

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 ...

Clinical Research Assistant

Dalton, GA · On-site

$19 - $33/hr

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 ...

Clinical Research Coordinator

Englewood, CO · On-site

$27.93 - $35/hr

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 ...

New

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 ...

Showing results 21-40

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 8, 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 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 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 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 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.
More about Overnight Clinical Research jobs
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, 71% Full Time, 18% 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 Assistant

Care Access

Brandon, FL

$19 - $33/hr

Full-time

Re-posted yesterday


Job description

About Care Access

Care Access is working to make the future of health better for all. With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly to communities that often face barriers to care. We are dedicated to ensuring that every person has the opportunity to understand their health, access the care they need, and contribute to the medical breakthroughs of tomorrow.

With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Through partnerships, technology, and perseverance, we are reimagining how clinical research and health services reach the world. Together, we are building a future of health that is better and more accessible for all.

To learn more about Care Access, visit www.CareAccess.com.

How This Role Makes a Difference

The Clinical Research Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while learning the skills necessary to be a Clinical Research Coordinator. This position has potential growth and advancement within the Care Access Research organization.

How You'll Make An Impact
  • Patient Coordination 
    • Obtain informed consent per Care Access Research SOP, under the direction of the CRC 
    • Complete visit procedures as required by protocol, under the direction of the CRC 
    • Collect, process and ship specimens as directed by protocol, under the direction of the CRC 
    • Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials. 
    • Request study participant payments 
    • Schedule visits with participants, contact with reminders 
    • Request medical records of potential and current research participants   
    • Complete basic clinical procedures, such as blood draws, vital signs, ECGs, etc., under the direction of the CRC  
    • Ability to understand and follow institutional SOPs   
  • Documentation 
    • Record data legibly and enter in real time on paper or e-source documents  
    • Update all applicable internal trackers and online recruitment systems 
    • Assist with recruitment of new participants by conducting phone screenings  
  • Patient Recruitment 
    • Assist with preparation of outreach materials  
    • Identify potential participants by reviewing medical records, study charts and participant database   
  • Other Responsibilities
    • Assist with query resolution   
    • Assist with administrative tasks such as copying, scanning, filing, mailing, emailing, etc.   
    • Assist with maintaining all site logs  
    • Assist with inventory and ordering equipment and supplies  
    • Interact in a positive, professional manner with patients/participants, sponsor representatives, Investigators and Care Access Research personnel and management. 
    • Communicate clearly verbally and in writing. 
    • Participate in recruitment and pre-screening events (may be at another location) 
    • Maintain effective relationships with study participants and other care Access Research personnel. 
The Expertise Required
  • Bilingual in Spanish required
  • Ability and willingness to work independently with minimal supervision  
  • Ability to learn to work in a fast-paced environment  
  • Excellent communication skills and a high degree of professionalism with all types of people
  • Excellent organizational skills with strong attention to detail  
  • A working knowledge of medical and research terminology  
  • A working knowledge of federal regulations, Good Clinical Practices (GCP)  
  • Critical thinker and problem solver  
  • Friendly, outgoing personality with the ability to maintain a positive attitude under pressure  
  • Contribute to team and site goals  
  • Proficiency in Microsoft Office Suite  
  • High level of self-motivation and energy  
  • An optimistic, "can do" attitude  
Certifications/Licenses, Education, and Experience
  • Minimum Experience:
    • A minimum of 1-year recent working experience as a Medical Assistant, EMT, LPN, Clinical Research Assistant or Phlebotomist.
    • Phlebotomy Experience and Proficiency Required
    • Some Clinical Research experience preferred  
How We Work Together
  • Location: This is an on-site position with regional commute requirements.
  • Travel: Regularly planned travel within the region will be required as part of the role. Overnight travel will be minimal (<10%).
  • Physical demands associated with this position Include: The ability to use keyboards and other computer equipment.
    • Walking - 20%, Standing - 20%, Sitting - 20%, Lifting (up to 25lbs, over 25lb, overhead) - 20%, Driving - 20%, Exposure to Bloodborne Pathogens - Yes

The expected pay range for this role is $19.00 - $33.00 USD per hour for full time team members.

Benefits & Perks (US Full Time Employees)
  • Paid Time Off (PTO) and Company Paid Holidays
  • 100% Employer paid medical, dental, and vision insurance plan options
  • Health Savings Account and Flexible Spending Accounts
  • Bi-weekly HSA employer contribution
  • Company paid Short-Term Disability and Long-Term Disability
  • 401(k) Retirement Plan, with Company Match

Mandatory Employer Disclosures:
Notice to Illinois applicants: Applicants are not obligated to disclose expunged juvenile records or adjudication, arrest, or conviction.
Notice to Connecticut applicants: Care Access may require applicants to submit to a urinalysis drug test in connection with an application for employment.
Notice to Arizona, Georgia, Indiana, and North Dakota applicants: Care Access complies with applicable laws prohibiting smoking in and around places of employment.
Notice to Massachusetts applicants: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Notice to Rhode Island applicants: Care Access complies with Rhode Island law prohibiting smoking in enclosed areas within places of employment. Care Access is also subject to is subject to Chapters 29–38 of Title 28 of the Rhode Island General Laws.
Notice to Maryland applicants: UNDER MARYLAND LAW, AN EMPLOYER MAY NOT REQUIRE OR DEMAND, AS A CONDITION OF EMPLOYMENT, PROSPECTIVE EMPLOYMENT, OR CONTINUED EMPLOYMENT, THAT AN INDIVIDUAL SUBMIT TO OR TAKE A LIE DETECTOR OR SIMILAR TEST. AN EMPLOYER WHO VIOLATES THIS LAW IS GUILTY OF A MISDEMEANOR AND SUBJECT TO A FINE NOT EXCEEDING $100.

Diversity & Inclusion

We work with and serve people from diverse cultures and communities around the world. We are stronger and better when we build a team representing the communities we support. We maintain an inclusive culture where people from a broad range of backgrounds feel valued and respected as they contribute to our mission.

We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to, and will not be discriminated against on the basis of, race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.

Care Access is unable to sponsor work visas at this time.

If you need an accommodation to apply for a role with Care Access, please reach out to: TalentAcquisition@careaccess.com