Clinical Safety Coordinator - Remote US

Sarah Cannon Research Institute•Nashville, TN

4d•Remote

About The Position

Our Safety Coordinator acts as the primary drug safety representative and contact for investigational sites, SCRI project teams for Investigator Initiated Trials (IITs) and Research Collaboration Trials. This is a fully remote position in the US; relocation assistance and visa sponsorship are not available. Duties include and are not limited to: Manage the receipt, processing, and electronic filing of IND Safety Reports (INDSRs) in alignment with SCRI policies and Sponsor-designated distribution methods Retrieve safety reports from sponsor/CRO portals or direct email and upload into the electronic repository with required metadata Support distribution of safety report metadata to investigators for review and acknowledgment via internal systems Other duties as assigned.

Requirements

Associate's Degree or Bachelor Degree preferred, experience may be substituted for education
Work experience with all Microsoft Office products including Excel, and varying software applications or databases
2+ years Data Entry experience in a hospital, medical office, or research environment requiring a high-level of attention to detail preferred
Experience and ability to appropriately manage and prioritize assigned tasks and adhere to specific deadlines

Responsibilities

Manage the receipt, processing, and electronic filing of IND Safety Reports (INDSRs) in alignment with SCRI policies and Sponsor-designated distribution methods
Retrieve safety reports from sponsor/CRO portals or direct email and upload into the electronic repository with required metadata
Support distribution of safety report metadata to investigators for review and acknowledgment via internal systems
Other duties as assigned