Clinical Research Coordinator II: Study Coordination & Data

UT Southwestern Medical Center; Dallas (TX); On-site; USD 55,000 - 70,000; Full time

Benefits offered by this job

PPO medical plan, available day one at

100% coverage for preventive health

Paid Time Off, available day one

Retirement Programs through TRS

Paid Parental Leave Benefit

Wellness programs

Tuition Reimbursement

Public Service Loan Forgiveness (PSLF)

Job summary

UT Southwestern Medical Center in Dallas recruits for a Clinical Research Coordinator role. You will coordinate research projects, directly interact with study participants via multiple channels, and support data collection and regulatory tasks.

A Bachelor’s degree in a medical or scientific field and 2 years of clinical research experience are required. The position involves handling regulatory documentation, IRB submissions, and coordinating with investigators, with opportunities for growth

Qualifications

• Bachelor's Degree in medical or science related field.
• 2 years clinical research experience.
• May consider additional years of experience or advanced degree in lieu of education or experience.

Responsibilities

• Interacts with clinical research participants via telephone, telehealth or in-person.
• Coordinates regulatory documentation for research studies including compliance with FDA requirements and IRB processes.
• Schedules procedures per research protocol and assists in consent processes when needed.
• Manages data collection and CRFs, and supports development of data collection tools.
• Provides training and ensures study team adherence to protocols and HRPP standards.

Education

Bachelor's Degree in medical or science related field

Tools

Clinical trial management system

Electronic Medical Records (EMR)

Job description

UT Southwestern Medical Center in Dallas recruits for a Clinical Research Coordinator role. You will coordinate research projects, directly interact with study participants via multiple channels, and support data collection and regulatory tasks.

A Bachelor’s degree in a medical or scientific field and 2 years of clinical research experience are required. The position involves handling regulatory documentation, IRB submissions, and coordinating with investigators, with opportunities for growth