CRA (Level II) - FSP
Thermo Fisher ScientificWhat You'll Do
Contributes to the selection of potential investigators and is accountable for study start-up and regulatory maintenance. Initiates, monitors, and closes study sites in compliance with AZ Procedural Documents. Ensures data query resolution in a timely manner and prepares monitoring visit reports in CTMS.
What We're Looking For
0 - 2 years of prior relevant experience in clinical research. Good knowledge of clinical research regulatory requirements, including GCP and ICH guidelines. Degree in a scientific discipline or healthcare.
Key Skills & Technologies
Additional Information
Experience Level
Junior
Job Language
English
Employment Type
Full-time
Work Mode
Remote