Description
The
Clinical Research Coordinator supports the operational management of clinical
research activities throughout the study lifecycle, including design, start-up,
conduct, and closeout. This role is responsible for implementing and managing
research activities for one or more studies, prioritizing tasks to meet
required deadlines. The Coordinator plans and organizes study activities to ensure
compliance with study protocols and applicable regulations, including
institutional policies, FDA Code of Federal Regulations (CFR), and ICH Good
Clinical Practice (GCP). The role involves close collaboration with the
Principal Investigator, ancillary departments, central research teams, sponsors,
and external institutions to support compliant study conduct, financial
management, and adequate staffing.

Hourly Salary Range: $36.37 - $58.52

Qualifications

Required:

+ Bachelors Degree or 1-3 years of previous study coo...