Description
At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.
As a Clinical Research Associate I, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programmes.
Responsibilities:
- Deliver clinical trial monitoring work to a high standard, working closely with your team and stakeholders.
- Coordinate all activities for setting up and monitoring a study, complete accurate study status reports, and maintain study documentation.
- Run sponsor-generated queries efficiently and take responsibility for study cost efficiency.
- 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:
- University degree in medicine, science, or equivalent.
- Knowledge of ICH-GCP guidelines and expertise to review and evaluate medical data.
- Previous experience in Oncology protocols.
- Excellent written and verbal communication in English.
- Good social skills enabling you to deal with queries in a timely manner.
- Willingness to travel as required (approximately 45%).
Rewards & Benefits:
- Competitive base salary and performance-related incentives.
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable.
- Retirement and pension plans.
- Life assurance and disability coverage.
- Employee assistance programmes and wellbeing resources.
- Learning and development opportunities through structured training and career pathways.