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Clinical Research Coordinator - Neurology and Neurotherapeutics

Job Number: 91807
Categories: Research & Laboratory
Location: 5323 Harry Hines Blvd, Dallas, TX
Department: 215002 - ODL-Core-NTRC
Full/Part Time/PRN: Day Job
Regular/Temporary: Regular


This position is security-sensitive and subject to Texas Education Code 51.215, which authorizes UT Southwestern to obtain criminal history record information


Salary Negotiable

Experience and Education

Master's degree in basic sciences, business administration, or related field and three (3) years progressive research/grant administration and coordination experience.

Bachelor's degree in basic sciences, business administration, or related field and five (5) years progressive research/grant administration and coordination experience.

Job Duties

Develops Quality Management Program for clinical research program to achieve accreditation.

Ensures regulatory compliance of clinical research program.

Develops and maintains website for marketing clinical research program.

Develops system for data collection and management of clinical research program registry information.

Coordinates development of clinical research program laboratory.

Coordinates interface between clinical research program and basic/clinical research collaborator at university and other institutions.

Provides general scientific support for clinical research program staff and university business office.

Assists in developing and implementing research studies to include writing clinical trials.

Other Job Duties

Duties performed may include one or more of the following core functions:
Directly interacting with or caring for patients
Directly interacting with or caring for human-subjects research participants
Regularly maintaining, modifying, releasing or similarly affecting patient records (including patient financial records);
Regularly maintaining, modifying, releasing or similarly affecting human-subjects research records.
Initially, the responsibilities would include mostly regulatory aspects of study start-up including completion of 1572 forms, FDA IND documentation, contracting between the institution and the sponsor and completion of IRB documents.
As the study progresses, the duties of the job would evolve to include screening, consenting and enrolling qualifying participants into the study protocol, randomizing subjects, organizing study visits, collecting, processing and shipping laboratory samples, completing all study procedures, maintaining and submitting all regulatory documents to the institution and sponsors, reporting adverse and serious adverse events, running samples from the hospital to the laboratory for processing and entering study data into electronic data capture systems.

UTSouthwestern Medical Center is committed to an educational and working environment that provides equal opportunity to all members of the University community. In accordance with federal and state law, the University prohibits unlawful discrimination, including harassment, on the basis of: race; color; religion; national origin; sex; including sexual harassment; age; disability; genetic information; citizenship status; and protected veteran status. In addition, it is UTSouthwestern policy to prohibit discrimination on the basis of sexual orientation, gender identity, or gender expression.

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