Upvote
Downvote
Senior Research Coordinator - Clinical Trials Unit
Share Job
- Suggest Revision
Full-time
- Overview: The Senior Research Coordinator in the Clinical Trials Unit will be primarily responsible for complex project management for multiple research studies related to psychiatric conditions in pediatric patients.
- The Senior Research Coordinator will ensure precise implementation of and adherence to study protocol, create all study documentation, oversee operating procedures, timelines, IRB applications, data preparation, and other research-related activities.
- In addition to operational management of multiple research studies, the Senior Research Coordinator will see patients participating in ongoing clinical trials, and will be responsible for specimen collection, processing, and DOT/ IATA compliant handling and shipment.
- Responsibilities: Prepare and submit Institutional Review Board (IRB) required materials, as well as prepare compliance and regulatory documentation for local, state, and federal agencies and any other pertinent entity.
- Create and maintain multiple IRB accounts and investigator notebooks and report adverse events.
Active Job
Updated TodaySimilar Job
Relevance
Active