Supervisor, Clinical Studies - Pediatrics Patient Care (Regulatory Team)

REQUIREMENTS

Education: Bachelor's degree in Science, Healthcare, Nursing, or a related field.

Preferred Education: Master’s degree in Science, Healthcare, Nursing, or a related field.

Preferred Certification: Certified Clinical Research Professional (CCRP) or Certified IRB Professional (CIP)

Experience: Six years of extensive research regulatory administrative experience in a biotechnology or academic setting, including three years of experience with research protocols, and clinical trials regulatory submissions. Three years of lead or supervisory experience is required.

Successful completion of the LEADing Self/Others Accelerate program may substitute for one year of required supervisory or management experience. May substitute required education degree with additional years of equivalent experience on a one-to-one basis. 

Preferred Experience: Clinical Trials Regulatory experience at MD Anderson.

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