Clinical Research Associate I
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Job Description
Clinical Research Associate I monitoring clinical trials for ICON, a global healthcare intelligence organization. Ensuring compliance and delivering high-quality outcomes in clinical programmes.
Responsibilities:
- Delivering clinical trial monitoring work to a high standard
- Working closely with your team and stakeholders
- Coordinating 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
- Participating in the preparation and review of study documentation and feasibility studies for new proposals as required
- Developing and maintaining strong, collaborative relationships with key stakeholders, clinical investigators, and site staff
- Ensuring patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements
Requirements:
- 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
- Willingness to travel as required (approximately 60%)
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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