Find clinical, allied health, care team, and healthcare operations openings using one smart search field across cities, regions, and employers.
4 C Medical Technologies
Overview
This role involves developing, coordinating, and administering the logistical aspects of clinical trials in compliance with GCP, GDP, and SOPs, acting as a key communication point between staff, sites, and vendors. Key duties include overseeing trial operations, managing site documentation, corresponding with study sites regarding subject progress and queries, and coordinating adverse event information.
Quick view →
Compensation
$75,000 - $95,000 / YEAR
Posted
7 days ago
Adventist Health
Performs technical research, database, and clerical duties to ensure adherence to study protocols and data quality. Coordinates with regional monitors, sponsors, and internal departments to manage regulatory documents and study progress.
$24 - $32 / HOUR
1 month ago
MEADOWHAWK BIOLABS INC
The intern will support laboratory operations, including the receipt, logging, storage, and disposition of study materials and samples, as well as managing inventory of consumables. Duties also involve waste collection, glassware cleaning, preparing basic chemical solutions, and maintaining laboratory cleanliness.
$18 / HOUR
2 months ago
Odyssey Systems Consulting Group, Ltd.
The Clinical Research Coordinator will provide research support for approved protocols, assist with patient recruitment, and ensure compliance with regulatory guidelines. Responsibilities also include maintaining documentation, managing study supplies, and collaborating with the Principal Investigator and research team.
Salary not listed
5 months ago
