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Full Time Clinical Trial Rn Jobs (NOW HIRING)

Frontier Medicines

Clinical Trial Manager

Boston, MA · On-site

$120K - $150K/yr

Traits we believe make a strong candidate: ● Bachelor's degree in a scientific, healthcare, or related field, or an RN, required. ● 3-4 years of Clinical Trial Manager or Clinical Project ...

Frontier Medicines

Clinical Trial Manager

Boston, MA · On-site

$120K - $150K/yr

Traits we believe make a strong candidate: • Bachelor's degree in a scientific, healthcare, or related field, or an RN, required. • 3-4 years of Clinical Trial Manager or Clinical Project ...

McLaren

Clinical Research Registered Nurse

Detroit, MI · On-site

Clinical Research (RN position - Detroit) Scheduled Bi-Weekly Hours: 80 Shift: Full-Time Day Daily ... Provides clinical trial support to ensure patients are offered appropriate clinical trials ...

CTI

Clinical Trial Manager

Covington, KY · Remote

Oversee the core clinical portions of the Trial Master File and ensure they are up-to-date and ... RN with Associate's Degree, or 3-year Nursing Diploma with at least 2 years clinical nursing ...

CTI

Clinical Trial Manager

Covington, KY · On-site +1

Oversee the core clinical portions of the Trial Master File and ensure they are up-to-date and ... RN with Associate's Degree, or 3-year Nursing Diploma with at least 2 years clinical nursing ...

CareDx, Inc.

Clinical Trial Manager

Brisbane, CA · On-site

Bachelor's degree in life sciences, health sciences or equivalent degree/experience; RN or ... to a full-time employee who makes the selfless act of donating an organ or bone marrow. With ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

$86K - $105K/yr

The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... Ability to travel as needed The anticipated annualized base pay range for this full-time position ...

Ardelyx

Clinical Trial Associate

Newark, CA

The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... Ability to travel as needed The anticipated annualized base pay range for this full-time position ...

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Full Time Clinical Trial Rn information

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How much do full time clinical trial rn jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for full time 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 Full Time Clinical Trial Rn vs Clinical Research Coordinator?

AspectFull Time Clinical Trial RnClinical Research Coordinator
CredentialsRegistered Nurse (RN) license, clinical trial trainingBachelor's degree, research training, sometimes certification
Work EnvironmentHospitals, clinics, research sites, hospitalsResearch sites, hospitals, clinics
Employer & IndustryPharmaceutical companies, research organizations, hospitalsResearch institutions, hospitals, CROs
Job FocusPatient care, administering trial protocols, data collectionStudy coordination, patient recruitment, data management

While both roles are vital in clinical research, a Full Time Clinical Trial RN primarily provides patient care and ensures protocol adherence from a nursing perspective. In contrast, a Clinical Research Coordinator manages study logistics, patient recruitment, and data collection. Both roles often collaborate but differ in their core responsibilities and required credentials.

What cities are hiring for Full Time Clinical Trial Rn jobs? Cities with the most Full Time 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 Full Time Clinical Trial Rn jobs? States with the most job openings for Full Time Clinical Trial Rn jobs include:
Full Time Clinical Trial Rn jobs near you

Clinical Trial Screening Coordinator

DM Clinical Research

Tomball, TX • On-site

Full-time

Re-posted 6 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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