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Overnight Clinical Research Coordinator Jobs in Columbus, OH

Centricity Research

Clinical Research Coordinator

Columbus, OH · On-site

$23.50 - $31.25/hr

About the role We are seeking a Clinical Research Coordinator I (CRC I) to join our research team. In this role, you will support the successful execution of clinical studies by performing a mix of ...

Centricity Research

Clinical Screening Coorinator

Columbus, OH · On-site

$23.50 - $31.25/hr

About the Role We're looking for a Clinical Screening Coordinator to lead research-related recruitment initiatives and ensure the enrollment of high-quality patients in accordance with Centricity ...

Actalent

Clinical Research Associate I

Westerville, OH

$25 - $27/hr

... clinical research of Gene Therapy products. This is a long-term career opportunity and we are ... coordination across internal teams and external partners. The position supports translational ...

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How much do overnight clinical research coordinator jobs pay per hour?

As of May 28, 2026, the average hourly pay for overnight clinical research coordinator in Columbus, OH is $27.71, according to ZipRecruiter salary data. Most workers in this role earn between $22.50 and $29.95 per hour, depending on experience, location, and employer.

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

AspectOvernight Clinical Research CoordinatorClinical Research Coordinator
Work HoursPrimarily overnight shiftsDaytime hours, flexible depending on study
CertificationsOften requires CPR, research certificationsSimilar certifications, may vary by employer
Work EnvironmentHospitals, clinics, research sites during night shiftsResearch centers, hospitals, clinics during day shifts
Job ResponsibilitiesMonitoring overnight patient visits, data collection, ensuring protocol adherence during night hoursParticipant recruitment, data management, study coordination during regular hours

In summary, the main difference lies in work hours and shift timing. Overnight Clinical Research Coordinators focus on night shifts, handling overnight patient visits and data collection, while Clinical Research Coordinators typically work during daytime hours managing various study tasks.

What are popular job titles related to Overnight Clinical Research Coordinator jobs in Columbus, OH? For Overnight Clinical Research Coordinator jobs in Columbus, OH, the most frequently searched job titles are:
What job categories do people searching Overnight Clinical Research Coordinator jobs in Columbus, OH look for? The top searched job categories for Overnight Clinical Research Coordinator jobs in Columbus, OH are:
What cities near Columbus, OH are hiring for Overnight Clinical Research Coordinator jobs? Cities near Columbus, OH with the most Overnight Clinical Research Coordinator job openings:
Overnight Clinical Research Coordinator jobs near you
Clinical Research Coordinator

Clinical Research Coordinator

Centricity Research

Columbus, OH • On-site

$23.50 - $31.25/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 24 days ago

Job description

Join Us at Centricity Research!
Centricity Research is one of the largest clinical research networks in North America. We are a fully centralized Integrated Research Organization (IRO) specializing in conducting Phase I-IV clinical trials in over 35 therapeutic areas: inpatient and outpatient; pharmaceutical, biotechnology, and medical device trials.
About the role
We are seeking a Clinical Research Coordinator I (CRC I) to join our research team. In this role, you will support the successful execution of clinical studies by performing a mix of administrative and clinical responsibilities. You will work closely with Investigators and the broader research team to ensure study activities are organized, compliant, and aligned with protocol requirements. This is an excellent opportunity to build your skills in clinical research and contribute to meaningful studies that impact patient care.
What you'll do
Study Coordination & Participant Safety
  • Conduct study visits in accordance with protocol, GCP, SOPs, and regulatory requirements
  • Ensure participant safety and well-being, reporting and documenting adverse events per protocol and regulations
  • Perform clinical procedures such as vitals, ECGs, sample collection/processing, and investigational product handling

Recruitment, Screening & Enrollment
  • Support recruitment strategies to identify and enroll eligible participants
  • Conduct participant screening according to protocol inclusion/exclusion criteria
  • Guide participants through the informed consent process and ensure proper documentation
  • Schedule and coordinate study visits throughout the participant lifecycle

Study Execution & Data Integrity
  • Accurately complete study documentation, regulatory records, and periodic reports
  • Prepare for and support monitoring visits, audits, and inspections
  • Perform regular quality control (QC) checks on study data and source documents
  • Collaborate with investigators, management, and sponsors to ensure study compliance and accuracy
  • Contribute to site start-up activities, including feasibility questionnaires (FQs) and pre-study visits (PSVs)

Quality, Compliance & Site Support
  • Prepare for monitoring visits, audits, and maintain regulatory files
  • Perform regular quality control checks on source data and documents
  • Support lab supply inventory, equipment maintenance, and administrative needs
  • Assist with community engagement and outreach events as needed

You Might Be a Great Fit If You:
  • Have a bachelor's degree in a health, science, or research-related field (or equivalent combination of education and experience)
  • Have 2-4 years of experience in a healthcare setting and are comfortable with clinical tools like blood pressure monitors, ECG machines, and weight scales (nice to have, but not required)
  • Have phlebotomy experience - or are open to learning it where permitted by law (we'll provide the training).
  • Understand basic medical terminology, or are eager to learn it quickly
  • Are passionate about contributing to clinical trials that impact global health
  • Are organized, detail-oriented, and skilled at multitasking in a fast-paced environment
  • Are proactive, collaborative, and take ownership of your work
  • Value open communication and thrive in a team-driven environment

Why Centricity Research?
Our Mission
We connect people to scientific advancements through groundbreaking research within a deeply human experience.
Our Core Values
  • Quality: We aim for excellence and integrity in everything we do - because lives depend on it.
  • Care: We show up for each other, our customers, and our mission - always going the extra mile.
  • Be the Change You Seek: We're adaptable, forward-thinking, and constantly improving - for the betterment of all.
  • One Team: We collaborate, support one another, and succeed together.
  • Grow for Good: We grow with purpose - to expand access to research and improve global health.
  • Own It: We take initiative, deliver results, and follow through - with passion and accountability.

Benefits
  • Comprehensive health, dental, and vision insurance
  • Enhanced EAP - mental health support
  • Flexible PTO + paid holidays
  • Continuing education reimbursement
  • 401(k) / RRSP with company match and immediate vesting

Ready to Apply?
We'd love to hear from you - apply now!
We're an equal opportunity employer committed to building a diverse and inclusive workplace. We welcome applicants from all backgrounds and will provide accommodations during the hiring process upon request.

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