Clinical Research Coordinator I: Patient-Centric Trials

UTSW

Town of Texas (WI)

On-site

USD 52,000 - 70,000

Full time

14 days+
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Job summary

UT Southwestern is seeking a Clinical Research Coordinator I to support a multidisciplinary research program and coordinate participant recruitment, screening, consenting, follow-up, and study visits. The role includes performing clinical procedures, managing CRFs/EDC/EPIC records, and ensuring compliance with GCP, IRB, and safety requirements.

Requires a Bachelor's degree in a medical or science field and 1 year of clinical research experience; BLS/CPR AED may be required by protocols or

Qualifications

  • Bachelor's Degree or higher degree in medical or science related field
  • 1 year of clinical research experience
  • May consider additional years of experience or advanced degree in lieu of education or experience, respectively.
  • (BLS) Basic Life Support Licensure may be required based on research study protocols or affiliate location requirements.
  • (CPRAED) CPR AED Licensure may be required based on research study protocols or affiliate location requirements.
  • ACRP or SOCRA certification a plus

Responsibilities

  • Directly interacts with clinical research participants, as required, for the research study.
  • Coordinate regulatory aspects of the trial including maintaining and developing regulatory information to comply with industry standards, University policies, FDA requirements or other hospital policies
  • Coordinate and schedule study procedures as per protocol.
  • Screen, recruit, enroll and follow subjects according to protocol guidelines.
  • Maintain and coordinate data collection information required for each study which may also include developing CRFs or data collection tools
  • Assist in developing and implementing research studies to include writing clinical research protocols.
  • Develop proficiency in the clinical trial management system, electronic medical record and other required data entry systems
  • Maintain subject level documentation
  • Duties performed may include one or more core functions: patient care, human-subjects research, or handling patient records
  • Performs other duties as assigned

Education

Bachelor's Degree or higher degree in medical or science related field

Job description

UT Southwestern is seeking a Clinical Research Coordinator I to support a multidisciplinary research program and coordinate participant recruitment, screening, consenting, follow-up, and study visits. The role includes performing clinical procedures, managing CRFs/EDC/EPIC records, and ensuring compliance with GCP, IRB, and safety requirements.

Requires a Bachelor's degree in a medical or science field and 1 year of clinical research experience; BLS/CPR AED may be required by protocols or

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