iconplc - IT - Administration

Lead regional clinical trial operations for a global CRO. This Boston or Philadelphia-based role requires 5-7 years' experience, including 3+ years in trial execution and direct team management. Oncology/hematology expertise is preferred. We offer a competitive salary, comprehensive benefits, and...

Seeking an Associate Director of Regional Clinical Operations to oversee clinical trials in the Southern US (Atlanta, Houston, Tampa, Dallas). This role requires 5-7 years in clinical operations, including 3+ years in trial execution and direct team management. Ideal candidates have global trial ...

Lead clinical data science initiatives for a world-leading CRO. Ensure data quality and integrity across studies from setup to database lock. Requires 6+ years' lead experience, including study start-up and 5+ database locks. Competitive benefits and flexible location options in Johannesburg, Rea...

Lead clinical trials from planning to completion as a Clinical Trial Manager at ICON Plc. Oversee timelines, budgets, and regulatory compliance while collaborating with cross-functional teams. This role requires a science/medicine degree, therapeutic expertise, and offers competitive benefits inc...

Join ICON plc as a Senior CTA and shape the future of clinical development. You will assist in designing and analyzing trials, interpret complex data, and advance innovative therapies. The role requires a scientific degree, clinical research experience, and excellent organizational skills. We off...

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 plc as a Senior Clinical Research Associate (CRA) in a home-based role in Germany. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. This role requires extensive CRA experience, strong site management skills, and a willingness to travel ...

Join ICON plc's dynamic team in Seoul as a Regulatory Affairs Specialist. You will design clinical trials, interpret medical data, and prepare key submissions (CT/IND, MAA/NA). This role requires 2-3 years of pharmaceutical regulatory experience. We offer competitive health insurance, retirement ...

Lead clinical trials remotely as a Clinical Operations Lead at ICON plc. Oversee planning, execution, and delivery of studies, ensuring compliance with timelines and regulations. This role requires a science/medicine degree, therapeutic expertise, and offers competitive health insurance and retir...

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...