iconplc - IT - Administration

Lead global clinical research projects as a Senior Project Manager at ICON plc in Barcelona. Utilize your pharmaceutical industry expertise to drive project execution and mentor teams. We offer competitive health insurance, retirement planning, and a supportive, innovative environment shaping the...

Lead clinical research projects as a dedicated Project Manager in Tel Aviv. You will oversee planning, execution, and delivery for a key sponsor, ensuring projects meet scope, time, and budget. Requires fluency in English/Hebrew, strong leadership, and PM experience. We offer competitive health i...

Lead pharmacovigilance safety initiatives at a global clinical research leader. Oversee a team ensuring regulatory compliance and risk management for clinical trials in Mexico City. Requires a life sciences degree and significant drug safety experience. We offer competitive health insurance and r...

Seeking a detail-oriented Clinical Research Coordinator for an office-based role in Gliwice/Bytom. You will support oncology studies, ensuring protocol and ICH-GCP compliance while managing site activities and data entry. This role requires fluency in English and Polish, along with proven oncolog...

Join ICON plc as a TMF Lead in Warsaw. Oversee Trial Master File management, ensuring regulatory compliance and integrity in clinical trials. Utilize your expertise in TMF processes within a world-leading clinical research organization. Enjoy competitive benefits including health insurance and re...

Join ICON plc as a Clinical Research Associate II in Frankfurt. You will design trials, analyze medical data, and ensure protocol compliance with 60% travel. Requires 2+ years CRA experience, ICH-GCP knowledge, and a scientific degree. We offer health insurance, competitive retirement plans, and ...

Join ICON plc as a Clinical Research Associate II in Dublin, Ireland. You will design and analyze clinical trials, ensuring protocol compliance and data integrity. This role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health insurance, retirement p...

Join ICON plc, a global clinical research leader, as a Senior CRA in France. This remote role requires 3+ years of independent monitoring experience in Pharma/Biotech/CRO. You will manage full site ownership across key therapeutic areas like Oncology and Neurology. Enjoy a competitive package wit...

Lead early-phase oncology trials as a Clinical Trial Manager at ICON in Raleigh or Blue Bell. Utilize your 5+ years of experience, including oncology and multinational trial management, to drive study success. This role offers competitive benefits and focuses on vendor oversight and regulatory co...

Lead complex clinical trial programs as a Trial Delivery Lead at ICON in Blue Bell. Utilize your extensive program management expertise to deliver large-scale projects on time and within budget. This role offers competitive benefits and requires strong leadership to guide cross-functional teams.

Join ICON plc as a Senior CRA in Guangzhou. You will conduct site monitoring, ensure protocol/GCP compliance, and contribute to advancing clinical trials. This role requires 2+ years CRA experience, deep trial knowledge, and 60% travel. We offer competitive health insurance, retirement plans, and...

Join ICON plc, a global clinical research leader, as a Clinical Trial Associate. This role focuses on study start-up support and vendor management within the US. We seek organized professionals with CRO/pharma experience and strong communication skills. Enjoy competitive benefits including health...