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Johns Hopkins University
Overview
Oversee day-to-day activities of complex oncology clinical studies and ensure operational feasibility of study designs. Manage participant recruitment, data collection systems, and maintain compliance with all applicable regulations and protocols.
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Compensation
$41,300 - $72,300 / YEAR
Posted
1 month ago
The Clinical Research Coordinator will manage the daily operations of clinical trials, ensuring adherence to study protocols and safety regulations. They will serve as the primary liaison between the Principal Investigator, regulatory agencies, and study participants while handling recruitment, data collection, and documentation.
$17 - $30 / HOUR
The Clinical Research Coordinator will manage the logistical implementation of clinical protocols and ensure adherence to study activities. They will also provide administrative support for regulatory issues, including IRB submissions and participant recruitment.
The Clinical Research Assistant will provide routine support to the research team by implementing clinical research protocols. Responsibilities include collecting study data through interviews and surveys, performing data entry, and maintaining communication with study participants.
$15 - $23 / HOUR
The Ophthalmic Technician provides clinical support to physicians by performing diagnostic eye tests, recording patient histories, and maintaining clinical equipment. They also assist with administrative tasks such as managing patient inquiries, processing forms, and ensuring clinic compliance with regulations.
$20 - $35 / HOUR
2 months ago
This role involves assisting the Ophthalmologist with patient care by learning and performing various ophthalmic tests, including obtaining accurate patient histories and performing basic skills like visual acuity measurement and lensometry. Key duties also encompass operating common ophthalmic equipment, performing basic tonometry, and maintaining examination rooms and instruments.
The coordinator will administratively manage the implementation of a clinical research protocol, ensuring efficient logistical execution and providing administrative support for regulatory matters. Key duties include coordinating all study activities to maintain protocol adherence and data validity, managing participant scheduling, and overseeing recruitment strategies.
3 months ago
The Clinical Research Assistant will provide routine support to the research team by implementing steps and processes of a clinical research protocol, including collecting study data via interviews, surveys, or clinical procedures. Responsibilities also involve performing data entry, organizing data, and assisting with routine contact with study participants.
