Pediatrics Research Coord II: Allergy/Immunology

Socket.dev

Dallas (TX)

On-site

USD 60,000 - 80,000

Full time

3 days ago
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Benefits offered by this job

PPO medical plan day one
Paid Time Off

Job summary

UT Southwestern Medical Center in Dallas, TX is seeking a Clinical Research Coordinator to coordinate patient/participant studies under minimal supervision. The role focuses on clinical data collection, regulatory compliance, and collaboration with sponsors and other institutions.

The position requires a Bachelor's degree in a medical or scientific field and at least 2 years of clinical research experience. Preferred certifications include BLS, CPR AED, and ACRP or SOCRA.

Qualifications

  • Bachelor's Degree in medical or science related field is required.
  • 2 years clinical research experience is required.

Responsibilities

  • Directly interacts with clinical research participants via telephone, telehealth or in-person.
  • Coordinates regulatory documentation to comply with industry standards, university policies, FDA requirements or other hospital policies.
  • Coordinates and schedules procedures per research study; may pend study order sets with PI oversight.
  • Screens, recruits, enrolls and follows subjects according to protocol guidelines, including consent processes.
  • Maintains and coordinates data collection information for each study; may develop CRFs or data collection tools.
  • Assists in developing and implementing research studies, including writing clinical research protocols.
  • Performs research procedures according to protocol with proper training.
  • Assists PI with fiscal management and budget preparation for trials.
  • Monitors patient safety by reviewing records and ensuring proper reporting per protocol and HRPP standards.
  • May perform research billing activities as needed.

Education

Bachelor's Degree in medical or science related field

Job description

UT Southwestern Medical Center in Dallas, TX is seeking a Clinical Research Coordinator to coordinate patient/participant studies under minimal supervision. The role focuses on clinical data collection, regulatory compliance, and collaboration with sponsors and other institutions.

The position requires a Bachelor's degree in a medical or scientific field and at least 2 years of clinical research experience. Preferred certifications include BLS, CPR AED, and ACRP or SOCRA.

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