Experience

i3 Research

• Senior Clinical Research Associate

  Responsibilities; Adapting and translating of study protocol and amendments and other study related documents, feasibilities and study star up coordination-EECC submission and approval + SIV. Assisting Regional Manager; SIV slides presentation, maintaining milestones in the project tracking system, creating newsletters and CRA study coordination; study status-cut off deadlines teleconferences, co-monitoring visits, routine monitoring visits (RMV) reports review and approval and time-sheets approvals. Others; discussing and finalizing investigators/hospital contracts with sites and legal department, study medication delivery supplies and SAEs reporting oversee and management. Type of visits; From feasibilities studies to close-out visits as CRA. Therapy areas and phases; Pneumology/Cardiology-Phase III and IIIb. Show less