Research Coordinator 1-Pediatrics

Responsibilities

• Plans and monitors the recruitment timetable in collaboration with the PI; submits weekly recruitment numbers/results to the PI.
• Reviews consents and data collected for study subjects for each study visit.
• Creates and maintains study logs for effective trial management; troubleshoots patient management problems/scheduling conflicts, etc. for assigned project(s).
• Devises and implements protocols and data gathering methods.
• Conducts protocol specific patient visits.
• Reviews and maintains source documentation and case report forms for completion and ensures confidentiality of subject records.
• Oversees the study lab specimens are collected/sent in an appropriate manner.
• Collects nasal swabs from study subjects.
• SUBMIT ORDERS FOR SUPPLIES OF ASSIGNED PROJECTS.
• Complies with the Clinical Trials Unit Manual of Procedures (MOP).
• Communicates with St. Jude study coordinators regarding IRB related issues.
• Gathers information for chart reviews, site visits, etc. as needed and distributes requested information appropriately.
• Performs other duties as assigned.

Qualifications

• EDUCATION: Bachelor’s Degree. (TRANSCRIPT REQUIRED)
• EXPERIENCE: One (1) year of research experience in subject recruitment, informed consent, understanding of IRB requirements, and following a research study protocol; OR a combination of education and experience to equal five (5) years.