Study Start Up Clinical Research Associate
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Coordinate study start-up and monitoring activities as a CRA I at ICON Strategic Solutions, with approximately 60% travel required. Use ICH-GCP knowledge to support clinical trials.
Working in a sponsor-dedicated model, you will contribute to ICON’s clinical trial operations function. The role covers study setup, monitoring, status reporting, documentation, and stakeholder collaboration. You will help deliver high-quality outcomes across clinical programmes while supporting patient safety and regulatory compliance.
Key Responsibilities:
- Coordinate study setup and monitoring activities independently
- Complete accurate study status reports and documentation
- Run sponsor-generated queries efficiently and support cost efficiency
- Prepare and review study documentation and feasibility studies
- Maintain relationships with investigators and site staff
Requirements:
- University degree in medicine, science, or equivalent
- Relevant clinical trial monitoring experience
- Knowledge of ICH-GCP guidelines and medical data evaluation
- Excellent written and verbal English communication
- Willingness to travel approximately 60% as required
Bring clinical monitoring, documentation, communication, and ICH-GCP expertise to ICON’s sponsor-dedicated clinical trial programmes.
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