iconplc - Hybrid work

Join ICON plc as a Senior Clinical Research Associate (CRA) in Mechelen. Independently manage all trial site activities from start-up to close-out, ensuring protocol and SOP compliance. Enjoy a competitive package with health insurance and support programs, while making a real impact on global pa...

Seeking a Senior Data Scientist specializing in Data Management for an office-based role in Blue Bell, PA or Raleigh, NC. You will design advanced models and algorithms, leveraging expertise in RCM processes and patient linkage methodologies. This role offers competitive benefits and the chance t...

Join ICON plc as a Senior Clinical Data Coordinator in Mexico City. Utilize your 5-7 years of experience with RAVE or Veeva to ensure data quality and regulatory compliance. You will develop data management plans, mentor junior staff, and collaborate with cross-functional teams. We offer competit...

Join ICON plc, a global clinical research leader, as a Set Up Specialist. You will coordinate clinical trial setup, ensuring regulatory compliance and efficient study execution. This role requires a life sciences degree and experience in trial setup or site management. The position offers competi...

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 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...

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...

Join ICON plc as an In-House CRA in Ankara. Utilize your life sciences degree and clinical research skills to support site management, document compliance, and data oversight. Enjoy a comprehensive benefits package while contributing to global clinical development in a collaborative, fast-paced e...

Join our team in Mexico City as a Regulatory Technician. You will manage clinical trial submissions using the CTIS system, ensuring compliance and quality. Ideal candidates have advanced English and 1-2 years in clinical research. We offer competitive health insurance and retirement plans.

Join ICON plc as a Senior Clinical Research Associate in Taipei. 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, r...

Join ICON plc, a global clinical research leader, as a Clinical Site Associate in Reading, UK. Support trial operations by ensuring site compliance, documentation accuracy, and audit readiness. This role requires a life sciences degree, strong organizational skills, and offers competitive benefit...