Clinical Research Coordinator I - Impactful Trials

UT Southwestern Medical Center; Dallas (TX); On-site; USD 60,000 - 75,000; Full time

Benefits offered by this job

PPO medical plan, day one coverage

100% preventive care coverage

Paid Time Off day one

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 I to coordinate research projects, primarily handling patient/participant coordination and data management for multiple studies. This role supports the UTSW Drug and Vaccine Allergy Program (UTSW-DVAP) with IRB protocol maintenance and recruitment efforts.

Key responsibilities include coordinating regulatory information, scheduling procedures per protocol, enrolling subjects, and maintaining data collection tools.

Qualifications

• Bachelor's Degree or higher degree in medical or science related field
• Experience 1 year of clinical research experience May consider additional years of experience or advanced degree in lieu of education or experience, respectively.
• Licenses and Certifications (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. Interacts via telephone, telehealth or in-person.
• 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. Approved study protocols which have order sets built may be pended by the non-licensed coordinator with oversight by PI.
• Screen, recruit, enroll and follow subjects according to protocol guidelines. May also assist with the consent process
• Maintain and coordinate data collection information required for each study which may also include developing CRF's or data collection tools
• Develop proficiency in the clinical trial management system, electronic medical record and other required data entry systems
• Maintain subject level documentation
• Perform other duties as assigned.

Skills

Participant coordination

Regulatory compliance

IRB protocol maintenance

Data collection

Clinical research

Patient recruitment

Education

Bachelor's Degree in medical or science field

1 year clinical research experience

Tools

Clinical Trial Management System

Electronic Medical Record (EMR)

Regulatory documentation

Job description

UT Southwestern Medical Center in Dallas, TX seeks a Clinical Research Coordinator I to coordinate research projects, primarily handling patient/participant coordination and data management for multiple studies. This role supports the UTSW Drug and Vaccine Allergy Program (UTSW-DVAP) with IRB protocol maintenance and recruitment efforts.

Key responsibilities include coordinating regulatory information, scheduling procedures per protocol, enrolling subjects, and maintaining data collection tools.