ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. What you will be doing: 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. Your profile: Bachelor's degree in a scientific or healthcare-related field. Experience monitoring Oncology, Obesity, and/or Gastrointestinal studies preferred. Minimum of 2 years of independent monitoring experience. 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. ICON offers a range of benefits including various annual leave entitlements, health insurance offerings, competitive retirement planning, a global employee assistance program, life assurance, and flexible country-specific optional benefits. ICON is committed to diversity, inclusion, and providing a workplace free of discrimination and harassment.
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