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Penn State University
Overview
The Human Research Technologist executes research protocols for clinical trials in Urology, focusing on participant recruitment and data collection. The role involves managing study visits, handling regulatory IRB submissions, and coordinating with principal investigators and sponsors.
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Compensation
$46,400 - $67,300 / YEAR
Posted
1 month ago
University of Miami
The Research Associate 1 supports clinical and community-based research activities, focusing on HIV prevention and related public health studies. Responsibilities include participant recruitment, data collection, and maintaining study records in compliance with protocols and regulations.
Salary not listed
Revival Research Institute, LLC
The Clinical Research Coordinator will manage multiple studies, assist Principal Investigators with participant recruitment, and handle data collection and specimen processing. They are also responsible for maintaining trial documentation, ensuring quality control, and communicating with study sponsors and the Institutional Review Board.
Irvine Clinical Research
The Clinical Research Coordinator will manage daily clinical operations, including performing study procedures and maintaining accurate study data. They are also responsible for recruiting and screening potential participants while conducting necessary diagnostic and safety assessments.
$25 / HOUR
Holmes County General Health District
The primary function involves maintaining and monitoring confidential information, scheduling participants, conducting eligibility interviews, and issuing WIC Nutrition Cards while explaining program rules. Additional duties include completing participant screenings, maintaining client charts, performing administrative tasks, and participating in breastfeeding promotion and outreach.
$11 - $16 / HOUR
Medical University of South Carolina
The program assistant will manage day-to-day research protocols, including participant recruitment, data collection, and entry for studies on addiction and interpersonal violence. They will also ensure regulatory compliance and supervise research staff to maintain high standards of data integrity.
$45,300 - $77,000 / YEAR
2 months ago
University of Rochester
The specialist will oversee the screening, assessment, and retention of participants in a Randomized Controlled Trial (RCT) involving Deaf adults with mental health disorders, conducting all study activities remotely via Zoom. Key duties include performing mental health and suicide risk assessments in ASL, coordinating follow-up assessments, assisting with data management, and ensuring participant safety according to protocol.
$21 - $30 / HOUR
Emory University
The Clinical Research Coordinator II manages administrative aspects of clinical trials, including maintaining databases, completing source documents, and providing guidance to junior staff. This role involves interfacing directly with research participants for eligibility determination and consent, as well as ensuring strict compliance with research protocols.
3 months ago
