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UHS
Overview
The Research Assistant will support Clinical Research Coordinators and Medical Directors by assisting with multiple research activities to ensure protocol efficacy and regulatory compliance, including data management projects as needed. Key duties involve ensuring appropriate patient scheduling according to protocol while maintaining confidentiality, and actively participating in the recruitment of study participants.
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Compensation
Salary not listed
Posted
1 month ago
Serv Recruitment Agency
The role involves supporting the day-to-day coordination of Phase I-III gynecologic oncology clinical trials, including managing regulatory files, tracking timelines, and coordinating patient visits and procedures. Responsibilities also include accurate data entry into EDC systems, maintaining audit-ready documentation, and assisting with regulatory compliance and monitoring visits.
2 months ago
CenExel
The Licensed Vocational Nurse is responsible for overseeing daily clinical study activities, serving as a liaison between the site and the Sponsor, and accurately documenting all research process information. Essential duties include providing general nursing care to participants, executing research protocols, screening subjects, and managing study documentation and supplies.
$30 - $33 / HOUR
3 months ago
The Registered Nurse is responsible for overseeing daily clinical study activities, serving as a liaison between the site and the Sponsor, and accurately documenting all research process information ethically. Essential duties include providing general nursing care, executing research protocols, screening subjects, and managing study documentation and supplies.
$39 - $43 / HOUR
