Clinical Studies Coordinator

EDUCATION:
Required: Bachelor's degree.

Preferred: Master's degree. 

EXPERIENCE:
Required: Three years experience in area of research study or direct patient care obtained from nursing, data gathering or other related experience. May substitute required education degree with additional years of equivalent experience on a one to one basis. With preferred degree, one year of required experience.

Preferred: Thorough understanding of protocol submission, maintenance, and compliance with IRB and experience in operation of clinical research protocols. Understands regulatory submissions process for phase 1 cell therapy trials. Understands clinical research study needs for cell therapy phase I trials, including obtaining patient consents and specimen collection during follow up visits.

It is the policy of The University of Texas MD Anderson Cancer Center to provide equal employment opportunity without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, disability, protected veteran status, genetic information, or any other basis protected by institutional policy or by federal, state or local laws unless such distinction is required by law. http://www.mdanderson.org/about-us/legal-and-policy/legal-statements/eeo-affirmative-action.html