iconplc

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...

Join ICON plc as a Global Study Manager in Reading, UK. Lead the design and analysis of global clinical trials, ensuring regulatory compliance. Utilize your 5+ years of trial management expertise to advance innovative therapies. We offer competitive benefits including health insurance and a suppo...

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 in Bangalore as a Senior Clinical System Designer. Lead end-to-end EDC study builds in Medidata Rave, ensuring high-quality database design and complex custom functions. Requires 5+ years of EDC experience and Rave proficiency. Enjoy competitive benefits including health insurance a...

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 Senior Clinical Research Associate in Johannesburg. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and participant safety. This role requires extensive CRA experience and a strong background in Respiratory studies, with 60% travel. We offer comp...

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 Senior Clinical Research Associate in Milan. 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 benefits including health insuranc...

Join ICON plc as a Senior Clinical Research Associate in Frankfurt. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. This role requires extensive CRA experience, strong site management skills, and 60% travel. We offer competitive health insurance...