job title: Clinical research associate 1 (icon plc)

Roles and Responsibilities

What you will be doing

• Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation

• Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of 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 ensuring compliance with ICON’s procedures, protocols, and regulatory requirements.

Your profile

• 1-4yrs of Experience into Onsite Monitoring

• 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 with queries in a timely manner

• Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid drivers license