Mineola, New York, United States
Experienced, Self-motivated clinical research professional with 10 years of experience managing, implementing, and coordinating research and administrative procedures for the successful management of clinical trials. A highly skilled leader adept in communicating and collaborating with diverse health care professionals, patients, and community members with a Master in Public Health.
Oversee NIH-funded research projects, provide guidance to the study team, and track deliverables. Responsible for regulatory activities for all projects. Help develop and submit progress reports to research sponsors. • Serve as liaison with stakeholders and external investigators for multi-institutional collaborative projects. • Coordinate the preparation and submission of grant applications to meet deadlines
In addition to Research Specialist responsibilities, coordinated, assisted, and managed departmental grant activities for pre and post award. Ensured timely submission of grants and progress reports. • Maintained, tracked, and updated effort tracking to ensure compliance with time and effort policies.
Coordinated academic research. Recruited subjects, reviewed research studies and obtained consent. Assumed responsibility for regulatory management of research protocols, including submission for CSEC, IRB, IACUC, ESCRO, CTSC, DSMB submissions.
Collaborated with principal investigators in conducting clinical research trials. Screened and enrolled subjects; tracked accrual goals. Performed data management, generated eligibility checklists and calendars. Advised the research team of required study evaluations. Efficiently processed and shipped biological specimens. Maintained study charts and inventory. Trained new data control assistants and coordinators.