Essential Functions
Complete required therapeutic protocol and clinical research training.
Gain experience in study procedures with support from senior clinical staff.
Conduct site monitoring visits (selection initiation monitoring close-out) per scope and GCP.
Train sites on protocol requirements and maintain ongoing communication.
Assess site compliance and escalate quality issues as needed.
Track study progress: regulatory submissions enrollment CRFs and data queries.
Maintain TMF/ISF documentation per GCP/ICH and local regulations.
Support study start-up activities.
Prepare visit reports follow-up letters and site management documentation.
Collaborate with study team members on project execution.
Learn and support site-level recruitment planning and progress tracking.
Qualifications
Fresh graduates () with a bachelors degree in a scientific or healthcare discipline.
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