Site Specialist II

ICON · Beijing, China · onsite ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a Site Specialist 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. 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. Your Profile Bachelor's degree in a scientific or healthcare-related field. Minimum of 3 years of experience as a Site Specialist. In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. Strong organisational and communication skills, with attention to detail. Ability to work independently and collaboratively in a fast-paced environment. Rewards & 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.