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Overnight Clinical Research Organization information

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$49K

$107.3K

$189K

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

As of Aug 27, 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:

Overnight Clinical Research Organization jobs near you

Clinical Research Coordinator Auburn AL

Medovation Clinical Research LLC

Auburn, AL • On-site

$22 - $28/hr

Part-time

Medical, Dental, PTO

Posted 8 days ago

Job description

Benefits
Competitive salary
Dental insurance
Health insurance
Paid time off
Training & development
About Us
We are an Integrated Clinical Research Organization dedicated to expanding access to clinical research and empowering physicians to bring advanced care options closer to diverse patient communities. We pride ourselves on fostering a collaborative and honest work environment where every team member takes ownership of their role.
Role Overview
Here's an opportunity to work for a dynamic and growing clinical research company. We have a fantastic and supportive work environment. The Clinical Research Coordinator plays a pivotal role in managing and overseeing clinical trials, ensuring compliance with regulatory requirements, and facilitating the smooth operation of research studies. This position works on-site at the physician’s practice. This position requires a detail-oriented individual with a strong background in medical terminology, data management, and clinical trials management. The ideal candidate will have at least two (2) years of experience coordinating all aspects of clinical research projects from initiation to completion. Phlebotomy skills required. 
Key Responsibilities
Manage the day-to-day operations of clinical trials, ensuring adherence to protocols and timelines.
Analyze data collected during trials and maintain accurate records for compliance management.
Oversee blood sampling procedures and ensure proper handling and documentation.
Train on clinical trial protocols and procedures.
Collaborate with healthcare professionals to ensure participant safety and integrity of data.
Utilize software for data capture and reporting
Maintain knowledge of medical terminology to effectively communicate with team members and stakeholders.
Ensure compliance with ethical standards and regulatory requirements throughout the research process.
Required Qualifications
Clinical experience preferred but not required
Experience in Sleep Clinical Trails preferred
Experience in clinical trials 2+ years of coordinator experience
Proficiency in data entry
Knowledge of medical terminology relevant to clinical research.
Phlebotomy and blood sampling techniques is required
Patient Recruitment experience required
Excellent organizational skills with attention to detail and the ability to manage multiple tasks simultaneously
What We Offer
A mission-driven and collaborative team culture.
Opportunities for career growth as the company scales.
The chance to contribute meaningfully to expanding access to clinical research for underserved populations.
If you’re looking for an opportunity to take ownership, build something from the ground up, and make a significant impact, we’d love to hear from you!
Compensation: $22.00 - $28.00 per hour
Medovation Clinical Research is an Integrated Clinical Research Organization dedicated to expanding access to clinical research and empowering physicians to bring advanced care options closer to diverse patient communities. We pride ourselves on fostering a collaborative and honest work environment where every team member takes ownership of their role. We value impactful work, open collaboration, and a spirit of diversity and inclusion.