Clinical Research Coordinator, RN at Cambay Healthcare LLC
Kingwood, Texas, USA -
Full Time


Start Date

Immediate

Expiry Date

04 Dec, 25

Salary

2130.0

Posted On

05 Sep, 25

Experience

1 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Clinical Research, Texas, Medical Records, Data Systems

Industry

Hospital/Health Care

Description

JOB TITLE: TRAVEL RESEARCH RN – NON-THERAPEUTIC

Location: Kingwood & Clear Lake, TX (Floating)
Schedule: Monday–Friday, 7:00 AM – 4:00 PM
Duration: 6 Months
Start Date: September 29, 2025

POSITION SUMMARY:

The Travel Research RN – Non-Therapeutic is responsible for coordinating and supporting multiple clinical research protocols at two healthcare locations in Kingwood and Clear Lake, TX. This position serves as a liaison between investigators, clinical staff, sponsors, and research personnel. The RN will assist with study coordination and patient care while gaining a solid foundation in human subject research and regulatory compliance.

QUALIFICATIONS:

  • Active Registered Nurse (RN) license in the state of Texas (or compact license)
  • Minimum 1 year of clinical research or related nursing experience preferred
  • Knowledge of clinical research regulations, GCP, and human subject protections
  • Ability to manage multiple protocols and prioritize tasks efficiently
  • Strong interpersonal, communication, and organizational skills
  • Proficiency in electronic medical records (EMR) and clinical data systems

How To Apply:

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Responsibilities
  • Float between Kingwood and Clear Lake research sites as needed
  • Coordinate all operational aspects of assigned clinical research studies
  • Serve as the point of contact between research personnel, sponsors, and internal departments
  • Perform and document patient assessments per protocol during study visits
  • Educate clinical staff on study protocols, assessments, and reporting requirements
  • Ensure accurate and timely documentation of study activities and subject data
  • Manage and report adverse events, protocol deviations, and related incidents
  • Complete medication order forms and obtain appropriate authorizations before treatment
  • Schedule patient follow-ups, imaging, and procedures per study timelines
  • Track and manage study-related shipments and supplies
  • Address and resolve data queries and ensure completion of case report forms
  • Perform patient re-consenting and document the process as per regulatory requirements
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