Clinical Research Associate
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Job Description
Entry-level Clinical Research Associate monitoring sponsor-dedicated clinical trials for ICON. Coordinating study activities, documentation, site relationships, compliance, and patient safety.
Responsibilities:
- Deliver clinical trial monitoring work to a high standard
- 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 collaborative relationships with key stakeholders, clinical investigators, and site staff
- Ensure patient safety and compliance with ICON's procedures, protocols, and regulatory requirements
Requirements:
- University degree in medicine, science, or equivalent
- Relevant clinical trial monitoring experience
- Knowledge of ICH-GCP guidelines
- 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
- Willingness to travel as required (approximately 60%)
- Legal right to work in the country where the role is based
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
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