Senior Clinical Research Coordinator

4 days ago


Canada Advanced Clinical Full time

At Advanced Clinical, we are seeking a Senior Clinical Research Associate to perform and coordinate all aspects of the clinical monitoring and site management process in accordance with ICH E6 Good Clinical Practices, FDA guidelines, local regulations, and standard operating procedures.

The ideal candidate will be responsible for performing the clinical monitoring aspect of designated projects in accordance with applicable SOPs; conducting clinical on-site monitoring activities, such as monitoring patient recruitment, reviewing consent forms, source data verification, drug accountability, data collection; collecting regulatory documentation; performing qualification, initiation, monitoring, and termination visits of investigational sites; writing visit reports; and completing all follow-up actions in accordance with ICH GCP guidelines.

This role requires strong clinical monitoring skills, a demonstrated understanding of medical terminology, and the ability to attain and maintain a working knowledge of Good Clinical Practices and applicable Standard Operating Procedures. Additionally, the successful candidate will possess flexibility, with the ability to travel up to 60-70% and work remotely.

We require a Bachelor's degree or RN degree and at least 4-5 years of monitoring experience, including strong start-up experience. Previous experience in Sickle Cell/Hematology or Respiratory is highly desirable.



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