Clinical Trials Safety Specialist - FDA Submissions

EDUCATION

Required: 

Bachelor's degree in a nursing, health science, or related field.

Preferred:

Master’s degree or other advanced degree in medicine or health science.

EXPERIENCE

Required:

Four years of clinical experience to include two years of clinical research. 

Preferred:
 
Five years of clinical experience to include two years of clinical research.

One year clinical trial safety reporting experience.  

LICENSURE / CERTIFICATION

Preferred:

Current license to practice professional nursing (RN), Advanced Oncology Certified Nurse (AOCN), Oncology Certified Nurse (OCN), Certified Clinical Research Professional (CCRP), Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Associate (CCRA), Regulatory Affairs Professional (RAP), or similar. 

OTHER

Onsite Presence: Seldom (0-5%)

Must pass pre-employment test as required and administered by Human Resources.

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.