ICON plc

Compensation

Full Description

Description: • 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 Requirements: • Bachelor's degree in a scientific or healthcare-related field highly preferred • Minimum of 2 years of experience as a Clinical Research Associate (on site monitoring experience required) • 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 Benefits: • Various annual leave entitlements • A range of health insurance offerings to suit you and your family’s needs • Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being • Life assurance • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others • Inclusion & belonging initiatives and a workplace free of discrimination and harassment