iconplc - Hybrid work

ICON seeks a Clinical Research Associate II in Hangzhou, China, to design and analyze clinical trials. You will ensure protocol compliance, data integrity, and patient safety while conducting site visits. Requires a Bachelor’s degree, 2+ years of CRA experience, and ICH-GCP knowledge. Benefits in...

Join ICON plc as a Clinical Data Coordinator I in Warsaw, Poland. You will design and analyze clinical trials, interpret medical data, and support innovative treatments. Requires a Master’s in Life Sciences or Healthcare, basic clinical data management knowledge, and familiarity with Medidata or ...

Join ICON plc as a Clinical Research Associate II in Taipei. You will design trials, analyze medical data, and advance new therapies. The role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer health insurance, competitive retirement plans, and flexible work arrange...

Join ICON plc as a Talent Sourcing Recruiter in Raleigh, NC. You will proactively build talent pipelines for critical clinical research roles across the US and Canada. This hybrid role requires sourcing passive candidates and utilizing ATS systems. We offer competitive health insurance, retiremen...

Join ICON plc, a global clinical research leader, as a Talent Sourcing Recruiter. Proactively build talent pipelines for critical roles in the US and Canada, engaging passive candidates in competitive markets. This contract role in Raleigh, NC, requires sourcing expertise, ATS proficiency, and pr...

Join our team as a Senior Clinical Validation Analyst in Bangalore. Utilize your 5+ years of EDC expertise, primarily in Medidata Rave, to validate and test clinical trial systems. You will lead UAT coordination, ensure compliance, and support study builds. We offer competitive health insurance, ...

Join ICON Plc as a Clinical Research Associate in Utrecht. Oversee clinical trials, ensuring protocol adherence, GCP, and data integrity. This role requires a life sciences degree, CRA experience, and 60% travel. We offer health insurance, competitive retirement plans, and global support.

Join ICON plc as a Clinical Research Associate (CRA) in Mechelen, Belgium. You will monitor clinical trial sites, ensuring protocol and GCP compliance. The role requires a life sciences degree, Dutch and English fluency, and proven monitoring experience. We offer competitive benefits including he...

Join ICON plc as a Clinical Site Associate in Tel Aviv. Support site management for clinical trials, ensuring efficiency and compliance. A life sciences degree and strong organizational skills are key. Enjoy a hybrid role with competitive health insurance and retirement benefits.

Join ICON as an HR Advisor in Sofia or Warsaw. Provide expert HR support and guidance across the employee lifecycle, using tools like Workday. This varied role offers project involvement and growth within a dynamic, global environment. Requires 3-4 years' HR experience, a relevant degree, and flu...

Join ICON plc as a Clinical Trial Assistant (CTA) in a hybrid role based in Sofia, Bulgaria. You will support clinical trial design, analysis, and document management using systems like eTMF. This role requires a scientific degree, trial process knowledge, and strong organizational skills. We off...