Clinical Research Coordinator II, Internal Medicine

WHY UT SOUTHWESTERN?
With over 75 years of excellence in Dallas-Fort Worth, Texas, UT Southwestern is committed to excellence, innovation, teamwork, and compassion. As a world-renowned medical and research center, we strive to provide the best possible care, resources, and benefits for our valued employees. Ranked as the number 1 hospital in Dallas-Fort Worth according to U.S. News & World Report, we invest in you with opportunities for career growth and development to align with your future goals. Our highly competitive benefits package offers healthcare, PTO and paid holidays, on-site childcare, wage, merit increases and so much more. We invite you to be a part of the UT Southwestern team where you'll discover a culture of teamwork, professionalism, and a rewarding career! 

JOB SUMMARY
Works under the direction of an Investigator(s) with limited supervision, to coordinate research projects. This position primarily performs patient/participant coordination, however, may conduct data management in smaller departments on as needed basis. Collects and ensures quality control of clinical or basic research data in support of multiple and/or complex research studies. 
 

The Department of Internal Medicine is seeking a Clinical Research Coordinator II to join the Clinical Trials Unit (CTU). The formation of the CTU is an initiative led by the office of the Internal Medicine Department Chair. As a valued team member, you will work with clinical trials from various divisions within Internal Medicine including but not limited to Cardiology and Hematology and will manage key aspects of the unit's investigational drug and device clinical trials. This includes determining effective strategies for recruiting trial participants, screening, consenting, and enrolling participants, and overseeing data management.  
 

BENEFITS
UT Southwestern is proud to offer a competitive and comprehensive benefits package to eligible employees. Our benefits are designed to support your overall wellbeing, and include:

• PPO medical plan, available day one at no cost for full-time employee-only coverage
• 100% coverage for preventive healthcare-no copay
• Paid Time Off, available day one
• Retirement Programs through the Teacher Retirement System of Texas (TRS)
• Paid Parental Leave Benefit
• Wellness programs
• Tuition Reimbursement
• Public Service Loan Forgiveness (PSLF) Qualified Employer
• Learn more about these and other UTSW employee benefits!

EXPERIENCE AND EDUCATION

Required

• Education
  Bachelor's Degree in medical or science related field 
   

• Experience
  2 years years clinical research experience. 
  May consider additional years of experience or advanced degree in lieu of education or experience, respectively. 
   

Preferred

• Licenses and Certifications
  (BLS) BASIC LIFE SUPPORT may be required based on research study protocols or affiliate location requirements. 
  (CPRAED) CPR AED may be required based on research study protocols or affiliate location requirements. 
  ACRP or SOCRA certification a plus. 
• Prior experience coordinating investigational drug or device clinical trials and/or industry sponsored clinical trials. 
   

JOB DUTIES

• Directly interacts with clinical research participants, as required, for the research study (non-clinical and clinical procedures). Interacts via telephone, telehealth or in-person.
• Coordinates regulatory documentation for research studies that includes m