Clinical Research Assistant I, Nephrology

Clinical Research Assistant I, Department of Internal Medicine - Nephrology

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 one of the world's foremost research institutions, UT Southwestern Medical Center is known for our life-changing research that has led us to 6 Nobel Prizes. With a career in our esteemed Internal Medicine Department, you will be a key part of our multidisciplinary research facility with opportunities to work with leaders in patient care and medical research. The Department of Internal Medicine Team at UT Southwestern is dedicated to providing exceptional patient-centered care. We seek to advance Internal Medicine through interprofessional education, leadership, and scientific discovery. 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

The Clinical Research Assistant I will be actively involved in the Preventing Cognitive Decline by Reducing BP Target (PCOT) research study. Duties include identifying possible participants, preparing study letters and sending letters to study candidates, recruiting participants to the study, obtaining informed consent, assisting with mailing and with step up of home blood pressure monitors and smart phone apps, administering cognitive tests, meeting study subjects in person and troubleshooting problems with study equipment, calling patients regularly to update BP readings if needed.

Experience and Education

Minimum Requirements

• High School diploma or GED with no experience.
• A minimum of Heart Saver for non-licensure or BLS for Licensure may be required based on research study protocols or affiliate location requirements.

Job Duties

May perform some or all of the following based on research study:

• Enters data into case report forms or other data collection system based on research study.

• Assists with maintenance of study level documentation.

• Assists with data queries and possible edits for accuracy.

• Compiles data for regulatory requirements and /or deadlines for local or sponsor submissions.

• Maintains existing databases and ensures data integrity.

• Understands visit schedules, inclusion/exclusion criteria and protocol requirements for routine and low complexity trials (e.g., questionnaire, data registry, scripted); schedules research visits.

• Assists research staff by completing research protocol related tasks.

• Assists with preparing annual reports and/or modifications to institutional review board (IRB). This may include reportable events (UPIRSO).

• Reviews and abstracts information from medical records including eligibility criteria.

• Recruits and enrolls patients in research study that may include consenting patients after training and with supervision.

• Assists with ordering and maintaining research supplies following university/department procedures, ensuring that equipment is in good working order.

• With adequate training and supervision, assists with collecting and processing specimens following established procedures/protocols.

• Assists in preparing studies for closeout, (e.g. packing files, documenting files for storage, shipping extra supplies back to sponsor).

• With adequate training/credentialing and supervision, performs study procedures such as phlebotomy, vital signs, and EKG's needed for research study.

• Based on research study, other procedures/equipment/services may be required.

• Duties performed may include one or more of the following core functions: a) Directly interacting with or caring for patients; b) Directly interacting with or caring for human-subjects research participants; c) Regularly maintaining, modifying, releasing or similarly affecting patient records (including patient financial records); or d) Regularly maintaining, modifying, releasing or similarly affecting human-subjects research records.

• Performs other duties as assigned.

Knowledge, Skills & Abilities

Possess strong computer skills (spreadsheets, databases, and interactive web-based software). Follows and understands the regulations for Protected Health Information (PHI). Proactively works to maximize results of the team and organization. Possess good communication skills. Possess the ability to problem solve. Work requires ability to conduct interviews with research subjects. Working Conditions Work is performed primarily in an office environment but may require periodic visits to clinical and off-site clinical areas for purpose of interviewing patients. May require local or out-of-state travel based on research study.

To learn more about the benefits UT Southwestern offers visit https://www.utsouthwestern.edu/employees/hr-resources/

For general COVID-19 information, applicants should visit https://www.utsouthwestern.edu/covid-19/work-on-campus/

This position is security-sensitive and subject to Texas Education Code §51.215, which authorizes UT Southwestern to obtain criminal history record information. UT Southwestern Medical Center is committed to an educational and working environment that provides equal opportunity to all members of the University community. As an equal opportunity employer, UT Southwestern prohibits unlawful discrimination, including discrimination on the basis of race, color, religion, national origin, sex, sexual orientation, gender identity, gender expression, age, disability, genetic information, citizenship status, or veteran status.