Hours: 40 hours per week
Responsibilities: Assists the Research Director with managing the research staff and clinical research studies being conducted in the Department of Research. Duties include developing Standard Operating Procedures and Manual of Procedures, overseeing and tracking research projects, case report from design, data collection, data entry, quality control, recruitment activities, and preparing study reports. Will have close working relationships with the Research Director, Principal Investigator, Co-Investigators, Study Coordinators and Project Managers to write protocols, reports, manuscripts, and grants for future funding.
Requirements: At least 5 years clinical trial management experience working in a research department or pharmaceutical environment. Thorough knowledge of IRB, HIPAA, and FDA regulatory requirements for the conduct of research required. Master’s degree in social science or public health required. Strong data management skills and experience with grant administration required.
Interested applicants, please provide interest letter and resume to Human Resources: