Licensed Study Coordinator

Job Summary

A company is looking for a Sr. Study Coordinator for a 6-month fixed-term position.

Key Responsibilities

• Support the screening process for potential participants and manage informed consent
• Coordinate patient telehealth visits and maintain accurate clinical data in compliance with GCP guidelines
• Manage investigational drug logistics and ensure regulatory compliance throughout the study

Required Qualifications

• Licensed Practical Nurse or equivalent license in the state of practice
• Minimum 2 years of study coordinator experience
• Strong understanding of GCP and research ethics
• Ability to work a flexible schedule, including on-call shifts
• Proficient in Microsoft Office Suite and electronic medical record (EMR) systems