Histologist
Posted 1hrs ago
Employment Information
Report this job
Job expired or something wrong with this job?
Job Description
Remote CRA I training as a Histologist for ICON’s sponsor-dedicated clinical trials. Monitoring studies, maintaining documentation, and supporting patient safety and regulatory compliance.
Responsibilities:
- Work in a sponsor-dedicated model supported by ICON’s global expertise
- Contribute to clinical trial operations and deliver high-quality outcomes across clinical programmes
- 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
- Pathology Lab experience
- 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%)
- 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

















