Note: The job is a remote job and is open to candidates in USA. ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. The Clinical Research Associate II will monitor Oncology studies in the northeast region, conducting clinical trial visits, ensuring protocol compliance and data integrity, collaborating with investigators and site staff, reviewing data, and contributing to study documentation.
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
- Experience monitoring Oncology trials
- 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%)
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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