iconplc - IT - Administration

Join ICON Plc as a Senior Clinical Research Associate in Beijing or Guangzhou. 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 60%. We offer ...

Join ICON plc as a Senior Clinical Research Associate in Frankfurt/Mannheim. Oversee clinical trials, ensuring protocol adherence, data integrity, and GCP compliance. Requires extensive CRA experience, strong site management skills, and 60% travel. Enjoy competitive benefits including health insu...

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

Join ICON plc, a global clinical research leader, as a Clinical Research Associate II in Kuala Lumpur. You will monitor sites, ensure protocol/GCP compliance, and contribute to advancing treatments. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel readin...

Join ICON plc as a Senior Clinical Research Associate (CRA) in the UK. Oversee clinical trial sites, ensuring protocol adherence, GCP, and data integrity. This role requires 3+ years' CRA experience, strong site management skills, and 60% travel. We offer competitive health insurance, retirement ...

Join ICON plc as a Pharmacovigilance Associate in Chennai. Process Clinical Trial cases using your LSMV database skills and 2+ years of PV experience. Ensure patient safety by analyzing adverse events and maintaining regulatory compliance. Enjoy competitive benefits including health insurance and...

Join ICON plc, a global clinical research leader, as a Clinical Trial Associate in Chennai. Utilize your scientific degree and organizational skills to coordinate trials and manage essential documentation. This role offers competitive benefits and a chance to contribute to innovative healthcare a...

Join ICON in San Antonio as a CMC Project Manager I. You will lead CMC projects for early-phase drug development, ensuring GMP compliance and coordinating cross-functional teams. This role requires 1+ years of project management experience in a pharmaceutical setting. We offer competitive health ...

Join ICON plc, a global clinical research leader, as a Project Manager I EDS. This hybrid role in Whitesboro, NY requires 3+ years of lab or project management experience. You will manage bioanalytical project timelines, budgets, and client coordination. We offer competitive health insurance, ret...

Lead global cell therapy trials in Hematology/Oncology as a Study Director. This senior role requires 7+ years of clinical trial experience, including 3+ in global study leadership. You will manage cross-functional teams to ensure timely, high-quality delivery. The position offers competitive ben...

Lead US clinical trials as a Local Study Associate Director at ICON plc. This role requires 5+ years of US trial management experience and deep ICH-GCP knowledge. You will oversee study commitments, lead local teams, and ensure regulatory compliance. We offer competitive health insurance, retirem...

Lead our Business Continuity Management in Ireland. Develop and implement robust continuity strategies, conduct risk assessments, and lead recovery planning. This hands-on role requires a CBCP/MBCP certification, 5+ years' experience, and a willingness to travel. We offer competitive benefits inc...