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Licensed Study Coordinator
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
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
