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Overnight Clinical Trials Jobs (NOW HIRING)

CBH Health

Clinical Research Coordinator I

Gaithersburg, MD · On-site

$26.90 - $34.35/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Job Summary: Responsible for assisting with coordinating clinical trials with the strictest ... Overnight travel may be required for training and/or investigative meetings. CenExel Clinical ...

CenExel

Clinical Research Coordinator I

Gaithersburg, MD · On-site

$26.90 - $34.35/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Job Summary: Responsible for assisting with coordinating clinical trials with the strictest ... Overnight travel may be required for training and/or investigative meetings. CenExel Clinical ...

CenExel

Clinical Research Coordinator II

Marlton, NJ · On-site

$26.24 - $33.51/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Job Summary: Responsible for coordinating all aspects of clinical trials with the strictest ... Overnight travel may be required for training and/or investigative meetings. CenExel Clinical ...

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Overnight Clinical Trials information

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How much do overnight clinical trials jobs pay per hour?

As of Aug 15, 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 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 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 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

Clinical Research Coordinator I

CBH Health

Gaithersburg, MD • On-site

$26.90 - $34.35/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 16 days ago

Job description

About Us:
CenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. Leading in CNS and early phase studies, our 18 science-led Centers of Excellence deliver the right patients, at the right time, in the right place. Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Our world-class PIs, advanced patient engagement strategies, premium data analytics, and integrated operations optimize every step of the clinical trial process.
Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation of, and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.
Job Summary:
Responsible for assisting with coordinating clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies.
Compensation: $26.90-$34.35 /hr depending on education, experience and skillset
Essential Responsibilities and Duties:
  • Assists with coordinating all aspects of patient involvement from study initiation until study completion.
  • Organizes research information for clinical trials.
  • Observes subjects and assists with data analysis and reporting.
  • Schedules the collection of data.
  • Documents adverse events, protocol deviations, and other unanticipated problems appropriately.
  • Reports research data to maintain quality and compliance.
  • Performs administrative and regulatory duties related to the study as appropriate.
  • Participates in other protocol development activities.
  • Ensures site receives accurate information and supplies from sponsors (i.e.: source, protocol, scales, supplies, approvals, contacts, etc.)
  • Educates potential participants and caregivers on protocol specific details and expectations.
  • Performs safety and efficacy assessments per protocol (vital signs, EKGs, blood draws and other assessments as assigned).
  • Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

Education/Experience/Skills:
  • High school graduate or equivalent; Bachelors Degree, preferred.
  • 0-3 years of experience in the medical field.
  • Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials.
  • Strong leadership and mentorship skills.
  • Developing and maintaining effective working relationships at all levels of the organization, along with those at the sponsor and vendor level.
  • Crisis management and problem solving skills; ability to react calmly and effectively in emergent situations.
  • Works independently as well as functioning as part of a team.
  • Must be able to effectively communicate verbally and in writing.

Working Conditions
  1. Indoor, Office environment.
  2. Shift work, depending on location.
  3. Essential physical requirements include sitting, typing, standing, and walking.
  4. Lightly active position, occasional lifting of up to 20 pounds. Rarely lift over 20 pounds.
  5. Reporting to work, as scheduled, is essential.
  6. 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 regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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