Regulatory Specialist I

University of Arkansas System•Little Rock, AR

16h•Onsite

About The Position

The University of Arkansas for Medical Sciences (UAMS) has a unique combination of education, research, and clinical programs that encourages and supports teamwork and diversity. We champion being a collaborative health care organization, focused on improving patient care and the lives of Arkansans. This position will be directly responsible for ensuring regulatory compliance and administrative management for multiple clinical trials, working closely with investigators, industry sponsors, contract research organization representatives, and UAMS institutional oversight offices. Workload will consist of industry-sponsored, foundation/private non-profit-sponsored, and investigator-initiated clinical trials. Position must be able to organize complex projects, provide attention to detail, and communicate effectively. Will apply knowledge of local policies and federal regulations and guidelines in support of an assigned clinical trial portfolio and the objectives of TRI. Contributes information and ideas related to areas of responsibility as part of a cross functional team. Ensures effective and efficient workflow and adherence to quality standards for staff/program and self. Position maintains a working knowledge of the Code of Federal Regulations and the code of conduct for human research. The employee will work directly with pharmaceutical company sponsors, institutional investigators, and research staff.

Requirements

Bachelor's degree or High School, GED, or formal education equivalent plus 4 years of research experience in lieu of bachelor’s degree.

Responsibilities

Ensuring regulatory compliance and administrative management for multiple clinical trials
Working closely with investigators, industry sponsors, contract research organization representatives, and UAMS institutional oversight offices
Organizing complex projects
Providing attention to detail
Communicating effectively
Applying knowledge of local policies and federal regulations and guidelines in support of an assigned clinical trial portfolio and the objectives of TRI
Contributing information and ideas related to areas of responsibility as part of a cross functional team
Ensuring effective and efficient workflow and adherence to quality standards for staff/program and self
Maintaining a working knowledge of the Code of Federal Regulations and the code of conduct for human research
Working directly with pharmaceutical company sponsors, institutional investigators, and research staff