Note: The job is a remote job and is open to candidates in USA. ICON is a global healthcare intelligence and clinical research organization dedicated to accelerating the delivery of new medicines and treatments to patients. The Clinical Research Associate, Histologist will be responsible for coordinating clinical trial monitoring activities, ensuring compliance with protocols, and maintaining strong relationships with stakeholders and site staff.

Responsibilities

• 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; you will also participate in the 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

Skills

• 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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