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Prisma Health
Overview
Responsible for the implementation, management, and oversight of clinical trial research studies, including patient visit management and data flow. Coordinates both investigator-initiated and industry-sponsored trials while ensuring compliance with protocols and regulatory agencies.
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Compensation
Salary not listed
Posted
26 days ago
Johns Hopkins University
This role involves the administrative coordination of research protocol implementation, ensuring efficient logistical execution of study activities and providing administrative support for all related matters. Key duties include coordinating study activities to maintain finding validity, developing operational plans with senior staff, and overseeing data collection and record management.
$17 - $30 / HOUR
2 months ago
University of Rochester
This role involves assisting in the planning, coordination, implementation, monitoring, and evaluation of assigned clinical research studies, ensuring adherence to regulatory guidelines from initiation to close-out. Key functions include coordinating participant enrollment, managing study documentation, performing data entry and quality checks, and maintaining study continuity for moderate-sized studies.
$25 - $35 / HOUR
3 months ago
University of Chicago
This role involves performing routine assignments for scientific research projects, ensuring compliance with all regulatory policies, and assisting in complex laboratory duties such as planning, execution, and organization of research activities. Responsibilities also include data collection, analysis, literature reviews, and contributing to the writing of academic papers and reports.
$24 - $34 / HOUR