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Overnight Clinical Trial Rn Jobs (NOW HIRING)

IQVIA

Clinical Trial Nurse

Houston, TX

$50 - $60/hr

We are seeking experienced Registered Nurses to conduct in-home visits and support clinical trial patients participating in groundbreaking research studies. This per diem opportunity offers flexible ...

McKesson

Clinical Trial Central Screener

Concord, NC

The Clinical Trial Central Screener (CTCS) will be responsible for centralized clinical support for ... Bachelor's Degree in Nursing or Licensed Registered Nurse * 3+ years of experience as a research ...

McKesson

Clinical Trial Central Screener

Concord, NC

The Clinical Trial Central Screener (CTCS) will be responsible for centralized clinical support for ... Bachelor's Degree in Nursing or Licensed Registered Nurse * 3+ years of experience as a research ...

Immatics NV

Clinical Trial Manager

$130K - $150K/yr

Bachelor's degree in life sciences, nursing, or a related field * 2+ years of experience in on-site clinical monitoring and 2+ years of Clinical Trial Manager experience within the pharmaceutical or ...

Mckesson

Clinical Trial Central Screener

Concord, NC

The Clinical Trial Central Screener (CTCS) will be responsible for centralized clinical support for ... Bachelor's Degree in Nursing or Licensed Registered Nurse * 3+ years of experience as a research ...

CareDx, Inc.

Clinical Trial Manager

Brisbane, CA · On-site

Bachelor's degree in life sciences, health sciences or equivalent degree/experience; RN or pharmaceutical experience preferred but not required * Minimum of 4 years of clinical trial management and ...

Icon plc

Clinical Trial Manager

Blue Bell, PA

Efficient communication with the Clinical Trial Managers (CTMs), Clinical Operations and the Global ... Willingness to travel with occasional overnight stay away from home according to business needs.

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Overnight Clinical Trial Rn information

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How much do overnight clinical trial rn jobs pay per hour?

As of Jun 20, 2026, the average hourly pay for overnight clinical trial rn 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 is the difference between Overnight Clinical Trial Rn vs Clinical Research Coordinator?

AspectOvernight Clinical Trial RnClinical Research Coordinator
CredentialsRegistered Nurse license, clinical trial trainingBachelor's degree, research training
Work EnvironmentHospital, clinical trial sites, overnight shiftsResearch sites, offices, daytime hours
Employer & IndustryHospitals, pharmaceutical companies, research institutionsResearch organizations, hospitals, universities
Job FocusPatient care, data collection during overnight shiftsStudy coordination, protocol management

Overnight Clinical Trial Rns primarily focus on patient care and data collection during overnight hours, requiring nursing credentials. Clinical Research Coordinators handle study logistics and protocol adherence during regular hours. Both roles are vital in clinical research but differ in responsibilities, work hours, and required qualifications.

What cities are hiring for Overnight Clinical Trial Rn jobs? Cities with the most Overnight Clinical Trial Rn job openings:
What are the most commonly searched types of Clinical Trial Rn jobs? The most popular types of Clinical Trial Rn jobs are:
What states have the most Overnight Clinical Trial Rn jobs? States with the most job openings for Overnight Clinical Trial Rn jobs include:
Overnight Clinical Trial Rn jobs near you
Clinical Trial Screening Coordinator

Clinical Trial Screening Coordinator

DM Clinical Research

Tomball, TX

Full-time

Posted 18 days ago

Job description

Clinical Trial Screening Coordinator
The Clinical Trial Screening Coordinator will act as a liaison between the recruitment and clinical trials teams to ensure that potential trial subjects are assigned to the trial best suited for them. To ensure that subjects have the required paperwork, medical records, and authorizations to participate in trials. To demonstrate effective knowledge of protocols, including inclusion/exclusion criteria. To demonstrate knowledge of Good Clinical Practices and FDA regulations specifically pertaining to the recruitment and retention of study subjects.
  • DUTIES amp; RESPONSIBILITIES
  • Completing DMCR-required training, including GCP and NIH.
  • Ensuring all patient enrollment activities are performed as per clinical trial protocol parameters by engaging directly with the CRCs and working closely with the clinical trial team.
  • Interfacing with potential research subjects to recruit, assess eligibility criteria, determine subject availability, assist investigators with obtaining informed consent and coordinate appointments with the recruitment team.
  • Managing pre-screen operational activities and establishing strong relationships with clinical trial sites and the staff.
  • Accountable for coordinating pre-screen data management activities - performing quality checks on timely data entry and data quality in the clinical research electronic system (CRIO).
  • Ensuring availability of study participant's information by accurately filing and/or retrieving study participant records as requested by management
  • Being prepared for and available at all required company meetings.
  • Submitting administrative paperwork per company timelines.
  • Any other matters as assigned by management.
KNOWLEDGE amp; EXPERIENCE
Education:
  • FMG (Foreign Medical Graduate) preferred or
  • Bachelors in Health Care Sciences or
  • Nursing Degree- LVN, LPN, or RN
Experience:
  • 3-4 years of Medical terminology
  • 1-2 years of customer service experience
  • 1-2 years of clinical research experience preferred
Credentials:
  • N/A
Knowledge and Skills:
  • Dependability
  • Medical Spanish a plus
  • Be an energetic, go-getter who is detail-oriented and can multi-task.
  • Be goals-driven while continuously maintaining quality.
  • Have attention to detail and accuracy.
  • Extreme attention to detail (strict adherence to procedures and protocols is essential)
  • Good knowledge of Good Clinical Practices and FDA regulations, protocols
  • Ability to use computer applications for data capture and for general communication required to
  • Communicate effectively, both orally and in writing

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