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Manager Clinical Trial Rn Jobs in Houston, TX (NOW HIRING)

IQVIA

Clinical Trial Rater

Houston, TX · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate Contract based About IQVIA ...

IQVIA

Clinical Nurse

Houston, TX · On-site

Management of Clinical Trial Patients * Provides complete patient assessment, including vital signs ... Current Registered Nursing License for the state the role is based in for RN's * Oncology ...

IQVIA

Clinical Nurse

Houston, TX · On-site

Management of Clinical Trial Patients * Provides complete patient assessment, including vital signs ... Current Registered Nursing License for the state the role is based in for RN's * Oncology ...

HiredFirst

Operating Room Clinical Manager RN

Cypress, TX · On-site

$89K - $134K/yr

A hospital in Cypress, TX is seeking a mid-level Operating Room Clinical Manager RN for a days-based, on-site leadership role. This position is responsible for overseeing clinical operations within ...

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All JobsClinical Trial Rn JobsManager Clinical Trial Rn JobsManager Clinical Trial Rn Jobs in Houston, TX

Manager Clinical Trial Rn information

See Houston, TX salary details

$27

$59

$91

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

As of Aug 26, 2026, the average hourly pay for manager clinical trial rn in Houston, TX is $59.70, according to ZipRecruiter salary data. Most workers in this role earn between $48.41 and $67.26 per hour, depending on experience, location, and employer.

What is the difference between Manager Clinical Trial Rn vs Clinical Research Coordinator?

AspectManager Clinical Trial RnClinical Research Coordinator
CredentialsRegistered Nurse (RN) license, clinical trial experience, possibly certification in researchTypically bachelor's degree in health or related field, research training
Work EnvironmentOversees multiple trials, manages teams, administrative and supervisory dutiesCoordinates daily trial activities, patient interactions, data collection
Employer & Industry UsagePharmaceutical companies, research institutions, hospitalsResearch sites, hospitals, clinics, academic institutions

The Manager Clinical Trial Rn generally has more supervisory responsibilities and clinical expertise, overseeing entire trials and managing staff. In contrast, the Clinical Research Coordinator focuses on daily trial operations and patient interactions. Both roles require research knowledge but differ in scope and seniority.

What are the most commonly searched types of Clinical Trial Rn jobs in Houston, TX?

The most popular types of Clinical Trial Rn jobs in Houston, TX are:

Manager Clinical Trial Rn jobs near you

Clinical Trial Screening Coordinator

Tomball, TX

DM Clinical Research
11 - 50 employees
Learn more about DM Clinical Researchexternal

Full-time

Re-posted 26 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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