Clinical Research Associate, Histologist
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Job Description
Clinical Research Associate at ICON responsible for high-quality clinical trial monitoring and compliance. Collaborating with stakeholders to ensure patient safety and adherence to protocols in clinical research.
Responsibilities:
- Delivering clinical trial monitoring work to a high standard, working closely with your team and stakeholders
- 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; participation in 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
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 30%)
- PHC Path Lab Lab experience or CRA experience is a plus
- Lab background (histology, pathology, Ultra, Ultra + experience) or IVD CRA experience desired
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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