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 general supervision, to primarily provide ongoing data management for local and national research studies. May coordinate observational (non-treatment) studies.
Additional responsibilities: Coordinates assigned human subjects research studies or defined components of larger clinical research projects through direct interaction with and providing care for patients or research participants. Leads day-to-day study operations, such as participant recruitment, informed consent processes, study visits, and protocol execution. This may include preparing and reviewing medical records, contacting patients by phone, conducting participant surveys, organizing logistics related to participant visits, entering and reviewing clinical data, and handling administrative tasks. Prepares, maintains, and organizes regulatory documents including IRB submissions, amendments, renewals, and study binders. Regularly maintaining, modifying, releasing or similarly affecting patient and research participant records. Ensures accurate, timely, and complete data collection and performs routine quality control and data reconciliation activities. Assists with biospecimen handling, processing, tracking, and shipment according to protocol and institutional guidelines, when applicable. Purchases office equipment, software, and laboratory supplies, maintaining inventory and expense records. Serves as a primary point of contact for assigned research projects. Assists with preparation of study reports, grant progress updates, abstracts, manuscripts, and other documents by organizing data and documentation. Provides functional guidance or training to new team members as assigned. Participates in quality assurance activities by preparing relevant data and documentation.
Preferred qualifications: Demonstrated experience coordinating clinical or human subjects research studies. Experience with IRB processes, regulatory documentation, and protocol implementation. Experience creating, managing and using REDCap Familiarity with Good Clinical Practice (GCP) and clinical trial workflows. Ability to manage multiple projects, meet deadlines, and work independently within a research team. Experience with phlebotomy and biospecimen handling and processing, including phlebotomy technician certification, experience handling and maintaining relevant equipment and preparing plasma, serum, whole blood, peripheral blood mononuclear cells and urine for long-term storage in -80C and liquid nitrogen. Interest in pursuing a career in clinical research, medicine, public health, or related health professions. Bilingual (English and Spanish)
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
High School Diploma or GED
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 affiliate location requirements
JOB DUTIES
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, 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.
SECURITY AND EEO STATEMENT
Security
This position is security-sensitive and subject to Texas Education Code 51.215, which authorizes UT Southwestern to obtain criminal history record information.
EEO
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.
