Regulatory compliance specialist with extensive experience in IRB compliance. Proven track record of ensuring adherence to regulatory standards and guidelines. Skilled in conducting audits and assessments to identify compliance gaps and implement corrective actions. Strong ability to collaborate with cross-functional teams to enhance compliance processes and training.
Overview
20
20
years of professional experience
Work History
Senior Research Assistant
Women and Infants Hospital
Providence, Rhode Island
11.2006 - 07.2026
Coordinated recruitment efforts for diverse clinical trials, enhancing participant engagement and retention.
Coordinated participant recruitment efforts for various clinical trials and studies.
Interviewed and enrolled clinical trial participants and explained scope of study.
Assisted with study recruitment, scheduling, administration of questionnaires and data collection.
Oversaw compliance with study protocols and regulations, safeguarding participant rights and data integrity.
Managed research documentation to ensure compliance with institutional protocols.
Maintained detailed documentation for research projects, ensuring adherence to institutional standards and facilitating audits.
Trained junior staff on research methodologies and data collection techniques.
Collaborated with faculty members on various aspects of the design, implementation, and evaluation of research studies.
Performed administrative duties such as scheduling meetings, preparing agendas, taking notes during meetings.
Clinical Research Coordinator & Clinical Assistant at Royal Victoria Hospital, McGill University Health CentreClinical Research Coordinator & Clinical Assistant at Royal Victoria Hospital, McGill University Health Centre