You’ll need
Education
✓4 years of research experience (5 years if no Masters degree) in data management and study coordination in healthcare or basic research.
Masters degree in Natural Sciences OR Bachelors degree in Natural Sciences plus 5 years of progressive research experience with some experience in research administration preferred.
Qualifications
✓Familiarity with IRB and human subjects research requirements preferred.
Experience with clinical research coordination, participant recruitment, or human subjects research preferred.
Strong organizational and interpersonal skills. preferred
Ability to communicate effectively with patients, investigators, and research staff. preferred
Experience with electronic research databases and data entry preferred.
Ability to maintain confidentiality and handle sensitive participant information. preferred
Ability to work independently while collaborating effectively with a multidisciplinary research team preferred
Benefits
Shift differentials
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Employer-posted ranges only
About the role
Assist with patient/participant recruitment and enrollment, including communicating with potential participants, providing study information, and coordinating screening and enrollment activities.
What you’ll do
Coordinate day-to-day research activitiesCoordinate day-to-day research activities and support the successful implementation of the study
Assist with patient/participant recruitmentAssist with patient/participant recruitment and enrollment, including communicating with potential participants, providing study information, and coordinating screening and enrollment activities
Conduct and coordinate studyConduct and coordinate study follow-up assessments with enrolled participants according to the study protocol
Participate in qualitative andParticipate in qualitative and quantitative data collection, including assisting with focus group coordination, facilitation, and coding
Enter research data andEnter research data and maintain accurate and up-to-date study databases at ISMMS