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Overnight Clinical Trials Jobs (NOW HIRING)

Actalent

Clinical Laboratory Assistant

Bucyrus, KS

Receive, accept, and accurately document biological samples collected during clinical trials ... Collaborate with a rotating group of day-shift staff, an evening staff member, and an overnight ...

Actalent

Clinical Laboratory Assistant

Bucyrus, KS · On-site

Receive, accept, and accurately document biological samples collected during clinical trials ... Collaborate with a rotating group of day-shift staff, an evening staff member, and an overnight ...

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Overnight Clinical Trials information

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$96

How much do overnight clinical trials jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for overnight clinical trials in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

What are overnight clinical trials?

Overnight clinical trials are research studies where participants are required to stay at a clinical facility for one or more nights. These trials are conducted to monitor the effects of experimental medications or treatments under controlled conditions, especially during sleep or over extended periods. Participants are closely observed by medical staff to ensure safety and collect accurate data. Such trials are essential for testing the safety, side effects, and efficacy of new drugs before they are approved for general use.

What are the key skills and qualifications needed to thrive as an overnight clinical trials coordinator?

To thrive as an Overnight Clinical Trials Coordinator, you need a solid understanding of clinical research protocols, data collection, and patient safety, typically supported by a degree in life sciences or nursing. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC), and adherence to Good Clinical Practice (GCP) guidelines is essential. Strong attention to detail, problem-solving skills, and the ability to communicate effectively during night shifts make candidates stand out. These skills are critical for ensuring accuracy, regulatory compliance, and participant well-being during clinical studies conducted outside standard hours.

What are some unique challenges faced by professionals working overnight shifts in clinical trials?

Working overnight in clinical trials often means adapting to irregular sleep patterns and managing fatigue, which can be challenging for some individuals. Overnight staff are responsible for monitoring participants, collecting data, and responding to any medical concerns that arise during non-traditional hours, requiring strong attention to detail and adaptability. Team communication is crucial, as overnight professionals must coordinate effectively with day-shift colleagues to ensure seamless participant care and accurate data handover. Despite the challenges, overnight roles can offer opportunities to develop specialized skills, take on additional responsibilities, and advance within clinical research operations.

What is the difference between Overnight Clinical Trials vs Clinical Research Coordinators?

AspectOvernight Clinical TrialsClinical Research Coordinators
CredentialsTypically require clinical trial experience, sometimes certifications like CCRPRequire degrees in health or related fields, often certifications like CCRP or CCRC
Work EnvironmentConducts trials during overnight hours, often in clinical settings or labsWork during regular business hours in hospitals, clinics, or research centers
Employer & IndustryPharmaceutical companies, research institutions, CROsHospitals, research institutions, pharmaceutical companies
Search & Comparison IntentFocuses on night shift clinical trial rolesFocuses on coordinating clinical research activities

Overnight Clinical Trials involve conducting clinical research during nighttime hours, often requiring specialized experience and night shift availability. Clinical Research Coordinators typically work during daytime hours managing and coordinating clinical studies. While both roles are essential in clinical research, they differ mainly in work hours and specific responsibilities.

What cities are hiring for Overnight Clinical Trials jobs?

Cities with the most Overnight Clinical Trials job openings:

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

The most popular types of Clinical Trials jobs are:

What states have the most Overnight Clinical Trials jobs?

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

Overnight Clinical Trials jobs near you

Neurologist Principal Investigator

Irvine Clinical Research

Long Beach, CA • On-site

$300K - $350K/yr

Full-time

Medical, Dental, Vision, PTO

Re-posted 15 days ago

Job description

Irvine Clinical Research is the largest independent clinical research site network on the West Coast. With 5 research centers in California, we are leaders in the search for new treatments in neurology, psychiatry, and obesity medicine. Our largest area of research is in Alzheimer's Disease prevention and treatment drug trials, and our doctors were the largest contributors in the world to the most recently FDA-approved medication in Alzheimer's Disease.
Irvine Clinical Research is hiring a Neurologist who will serve as a Principal Investigator. The physician will oversee Phase 1, 2, and 3 clinical trials of some of the most promising drugs under investigation in memory disorders and other neurological conditions. This includes next-generation disease-modifying anti-amyloid therapies in the same class as donanemab and lecanemab, anti-tau agents, and novel therapies like antisense oligonucleotides (ASOs).
Our hiring needs vary per location (Inglewood, Long Beach, Oakland, Riverside), so please indicate any preferred locations in your application.
Job Duties
  • Lead study team as a Principal or Sub-Investigator, ensuring trials are conducted safely and per protocol
  • Conduct clinical intake interviews to determine medical eligibility of potential study participants
  • Educate potential participants about diseases and the benefits of clinical trial participation
  • Manage the safety of study participants; respond appropriately to adverse events in a timely manner
  • Perform cerebrospinal fluid collection (lumbar puncture) in diagnostic and therapeutic studies
  • Provide medical leadership to our team of psychologists and study coordinators

Job Requirements
  • Valid license to practice medicine in California (or license-eligible)
  • Board-certified in neurology or psychiatry
  • Experience working with older adults in a clinical or research setting
  • Clinical research experience is preferred, but not required
  • A command of professional spoken and written English

$300,000 - $350,000 a year
Hours and Compensation
This is a full-time employment position based in-person at one of our clinics (Riverside, Inglewood, Long Beach, or Oakland). There are no planned overnight or weekend hours.
The starting salary for this position is $300,000 per year. Higher salary is available with candidates meet one of the following criteria: (1) current/previous investigator in pharmaceutical clinical trials of Alzheimer's Disease (2) superior skill in intrathecal administration and CSF collection in clinic.
The company pays for 100% of health/dental/vision individual insurance costs for eligible full-time employees. Vacation (PTO) is earned at a rate of 3 weeks per year.

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