iconplc - Remote work

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 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...

Join ICON plc as a Senior Clinical Research Associate in Oslo. Oversee clinical trials, ensure ICH-GCP compliance, and analyze data. Requires fluency in Norwegian and English, plus 60% travel. Enjoy health insurance, competitive retirement plans, and a global support program.

Seeking an experienced Senior Clinical Research Associate (CRA) for oncology trials in the Midwest. You will monitor sites, ensure GCP compliance, and manage stakeholder relationships. This role offers competitive benefits including health insurance and requires extensive CRA experience with onco...

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 as a Clinical Research Associate II in a remote role based in Colombia. 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 insuran...

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...