iconplc - IT - Administration

Join ICON plc as a Senior Clinical Research Associate in Seoul. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Utilize your extensive CRA experience and monitoring expertise, with 60% travel. Enjoy competitive health insurance, retirement plann...

Regulatory Affairs Associate needed in Seoul, South Korea. Leverage 3+ years of clinical regulatory experience, including IND submissions and CMC, to drive study start-up activities. Ensure compliance, manage ethics submissions, and safeguard patient welfare through informed consent review. Benef...

Seeking an experienced **Clinical Trial Manager** in **Seoul, South Korea** to lead complex PMS projects. Requires 7+ years of clinical research experience with a proven track record in project leadership and cross-functional team management. You will oversee trial protocols, budgets, and regulat...

Join ICON as a Medical Research Associate in San Antonio. You will greet volunteers, check vitals, and support clinical trials with data collection and documentation. Requires a High School Diploma, medical assistant certification or allied health credential (e.g., EMT, LVN), and strong organizat...

Clinical Team Lead, Site Operations role in Hickory, US. Lead and mentor site operations staff, overseeing start-up, maintenance, and close-out tasks. Requires a Bachelor’s degree in life sciences or equivalent clinical research experience, plus strong leadership and GCP knowledge. Enjoy competit...

Lead innovative training development at ICON in Belfast, UK. This role designs cutting-edge learning solutions for clinical research, pharmacovigilance, and regulatory teams. Requires 5+ years in learning design, expertise in Articulate 360 and Vyond, and strong project management skills. Enjoy b...

Join ICON Plc as a Clinical Research Associate II in Shanghai, China. Oversee global clinical trials, ensure ICH-GCP compliance, and manage study documentation. Requires a science degree, strong communication skills, and 60% travel. Enjoy competitive benefits including health insurance, retiremen...

ICON seeks a Clinical Project Manager for Post Trial Access in Gdansk, Poland. You will lead global PTA programs for investigational products, managing timelines, budgets, and cross-functional teams. Requires 2+ years in clinical research or biopharma, with expertise in regulatory frameworks and ...

Join ICON plc as a Clinical Research Associate in multiple US locations. Leverage your onsite monitoring experience and ICH-GCP expertise to oversee oncology and multi-therapy trials. Enjoy competitive benefits, health insurance, and retirement plans while advancing innovative treatments. Travel ...

Join ICON as a Clinical Research Associate II (CRA II) in Shanghai, China. Leverage 2+ years of experience and ICH-GCP expertise to design, monitor, and analyze clinical trials. Ensure protocol compliance and data integrity while traveling up to 60%. Enjoy competitive benefits including health in...

Senior Clinical Research Associate sought by ICON Plc in Frankfurt, Germany. Manage and monitor clinical trials, ensuring GCP and regulatory compliance across multiple sites. Requires a Bachelor's in a scientific field, extensive CRA experience, and strong site management skills. Benefit from com...

Join ICON as a Clinical Research Associate II (CRA II) in Milan, Italy, focusing on late-phase and real-world studies. You will conduct site monitoring for interventional, observational, and medical device trials, ensuring ICH-GCP compliance and high-quality data collection. Ideal candidates have...