Tasks

  • Support the clinical operations team in managing trial documentation, site communication, and study supplies
  • Maintain and update trial information in CTMS and eTMF systems
  • Coordinate contracts, insurance certificates, and vendor-related activities
  • Assist with SOP reviews, team meetings, and cross-functional collaboration

Qualifications

  • Minimum 2 years of experience in clinical research preferred
  • Strong organizational and communication skills in English
  • Proficient in MS Office and able to manage multiple priorities independently
  • Detail-oriented, team player, and results-driven