Responsibilities

• Work independently to coordinate all activities for setting up and monitoring a study, completing accurate study status reports, and maintaining study documentation.
• Run sponsor–generated queries efficiently and manage study cost efficiency. Prepare and review study documentation and feasibility studies for new proposals as required.
• Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
• Ensure patient safety by adhering to ICON’s procedures, protocols, and regulatory requirements.

Qualifications

• University degree in medicine, science, or equivalent.
• Knowledge of ICH–GCP guidelines and the expertise to review and evaluate medical data.
• Excellent written and verbal communication in English.
• Good social skills enabling you to deal wi...