iconplc

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 an Accounts Receivable Associate in Chennai or Trivandrum. You will manage the full Contract-to-Cash billing cycle, ensuring accurate invoicing and compliance. The role requires 2-3 years' AR experience, outstanding Excel skills, and collaborat...

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...

Join ICON plc, a global clinical research leader, as a Clinical Study Coordinator in Salt Lake City. You will design trials, analyze medical data, and advance innovative therapies. The role requires a scientific degree, GCP knowledge, and strong organizational skills. We offer competitive benefit...

Join ICON plc as a Payment Analyst in Warsaw. Utilize your finance degree and 1-2 years' experience to ensure compliant investigator payments for clinical trials. You will process payments, resolve discrepancies, and streamline procedures in a dynamic, global environment. We offer competitive ben...

Join ICON as a Commercial Legal Counsel in Warsaw. Provide pragmatic legal advice and negotiate complex agreements for Pharma and Biotech clients. Leverage 2-5 years of in-house or law firm experience in commercial contracts. Enjoy competitive benefits including health insurance and a global supp...

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...