Clinical Trials Coordinator

Responsibilities

Working under minimal supervision, the Clinical Trials Coordinator is responsible for study subject identification, recruitment, screening for eligibility, enrollment, and follow-up in accordance with research protocols. The Coordinator will initiate all regulatory documentation and maintain compliance. As a Patient Navigator, the Coordinator will provide orientation, scheduling, retention, and transportation assistance for study subjects.

• Bachelor’s degree in Physical Sciences (biology, chemistry, physics, etc.) or Healthcare/Public Health or related field.

• Clinical Trial Coordinator certification Level 2 or 3 (CCRC/CCRP or related Clinical Research Certification).

• 1 year of professional level experience (CTC
1). 3 years of professional level experience (CTC
2). 5 years of professional level experience (CTC
3).

• Master’s degree can substitute for 1 year of professional level experience.

Preferred qualifications were not specified.

LSU Health New Orleans seeks candidates who will contribute to a climate where students, faculty, and staff of all identities and backgrounds have equitable access and success opportunities. As an equal opportunity employer, we welcome all to apply without regard to race, color, religion, age, sex, national origin, physically or mentally disabled, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

LSU Health New Orleans is also a State As a Model Employer (SAME) agency and provides assistance to persons needing accommodations or with accessibility of materials. For those seeking such accommodations or assistance related to this search, we encourage you to contact the Office of Human Resource Management (
HRMADA
).