Clinical Research Coordinator
CurrentResponsible for coordinating all aspects of a multi-site clinical trial in conjunction with the study's Principal Investigators at the Philadelphia and Coatesville VAMCs. Responsibilities include:Complete and submit all regulatory reviews, protocol amendments, and event reports to the respective site IRBs and other oversight committees. Lead the recruitment, eligibility screening, and informed consent of all prospective study subjects. Schedule and conduct all 16+ research visits for each study subject.Ensure that all data is collected accurately, completely, and at the correct time point during the 6-month long study protocol.Maintain subject confidentiality and HIPAA-compliance in all study activities. Mentor and direct student research assistants in the completion of study-related projects. Complete statistical analysis of datasets, and develop abstracts and manuscripts summarizing findings.