Clinical Research Coordinator II: Lead Multi-Study Trials

University of Texas Southwestern Medical Center

Dallas (TX)

On-site

USD 55,000 - 75,000

Full time

3 days ago
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Benefits offered by this job

PPO medical plan
Preventive care coverage
Paid Time Off
TRS retirement programs
Paid Parental Leave
Wellness programs
Tuition Reimbursement
PSLF Qualified Employer

Job summary

UT Southwestern Medical Center in Dallas, TX, seeks a Clinical Research Coordinator to support multiple studies. The role involves coordinating participant interactions, data collection, and regulatory documentation under supervision of investigators.

The position requires a bachelor’s degree in a medical or science-related field and at least 2 years of clinical research experience, with preferred certifications (BLS/CPR AED; ACRP or SOCRA).

Qualifications

  • Bachelor's Degree in medical or science related field.
  • 2 years clinical research experience; additional years or advanced degree may substitute.
  • Licenses and Certifications: BLS/CPR AED may be required; ACRP or SOCRA certification a plus.

Responsibilities

  • Directly interacts with clinical research participants via telephone, telehealth or in-person.
  • Coordinates regulatory documentation for research studies per industry standards and policies.
  • Schedules procedures per protocol; may pend study order sets with PI oversight.
  • Screens, recruits, enrolls and follows subjects per protocol; may assist with consent.
  • Manages data collection and develops CRFs or data tools.
  • Assists in developing/implementing research studies and writing protocols.
  • May assist PI with budget management and billing related tasks.
  • Monitors patient safety per HRPP standards; may link calendars for billing.

Education

Bachelor's Degree in medical or science related field

Job description

UT Southwestern Medical Center in Dallas, TX, seeks a Clinical Research Coordinator to support multiple studies. The role involves coordinating participant interactions, data collection, and regulatory documentation under supervision of investigators.

The position requires a bachelor’s degree in a medical or science-related field and at least 2 years of clinical research experience, with preferred certifications (BLS/CPR AED; ACRP or SOCRA).

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