Note: The job is a remote job and is open to candidates in USA. ICON is a global healthcare intelligence and clinical research organisation focused on bringing new medicines and treatments to patients faster. The Clinical Research Associate - Central will conduct and support clinical trial monitoring activities, including site visits, protocol compliance, data review, investigator collaboration, and study documentation, with a focus on Ophthalmology or multiple therapeutic areas.
Responsibilities
- Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials
- Ensuring protocol compliance, data integrity, and patient safety throughout the trial process
- Collaborating with investigators and site staff to facilitate smooth study conduct
- Performing data review and resolution of queries to maintain high-quality clinical data
- Contributing to the preparation and review of study documentation, including protocols and clinical study reports
Skills
- * Bachelor's degree in a scientific or healthcare-related field
- * Minimum of 2 years of experience as a Clinical Research Associate
- * In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
- * Strong organizational and communication skills, with attention to detail
- * Ability to work independently and collaboratively in a fast-paced environment
- * Willingness to travel as required (approximately 60%)
- Employment with ICON is contingent upon having the legal right to work in the country where the role is based
- Our client is looking for candidates with experience monitoring Ophthalmology trials or multi-TA
Benefits
- 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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