Full employer posting
The Associate Researcher I will support the implementation and day-to-day coordination of the research study under the supervision of Drs. Ash Tewari ad Dr. Nihal Mohamed.
The Associate Researcher I will work closely with the Principal Investigators, Co-Investigators, and research team to support participant recruitment and follow-up, qualitative and quantitative data collection, regulatory activities, study database management, and overall project coordination. Responsibilities Coordinate day-to-day research activities and support the successful implementation of the study. Assist with patient/participant recruitment and enrollment, including communicating with potential participants, providing study information, and coordinating screening and enrollment activities.
Conduct and coordinate study follow-up assessments with enrolled participants according to the study protocol. Participate in qualitative and quantitative data collection, including assisting with focus group coordination, facilitation, and coding. Enter research data and maintain accurate and up-to-date study databases at ISMMS.
Ensure accurate and timely collection, documentation, and management of research data. Prepare and submit regulatory documents required for human subjects research at ISMMS under the supervision of the Principal Investigators. Coordinate Institutional Review Board (IRB) submissions, continuing reviews, amendments, and other regulatory activities throughout the study.
Coordinate research meetings and maintain communication among the research team and study collaborators. Organize and participate in weekly and biweekly research team meetings. Assist the Principal Investigators and Co-Investigators with preparation of continuation and final reports, manuscripts, presentations, and other study-related materials.
Maintain study documentation and ensure compliance with institutional and study-specific policies and procedures. Perform other research coordination activities as needed to support successful completion of the study. Qualifications Bachelors or Masters degree in science or related field required No experience required.
One year of research experience preferred.
Full time · Day shift
About the role
Assist with patient/participant recruitment and enrollment, including communicating with potential participants, providing study information, and coordinating screening and enrollment activities.