iconplc

Join ICON plc, a global clinical research leader, as a Site Management Associate I in Kuala Lumpur. Support site monitoring and ensure protocol/GCP compliance in a dynamic team environment. A relevant degree and strong organizational skills are key. Enjoy competitive health insurance, retirement ...

Join ICON plc, a global clinical research leader, as a Clinical Trial Assistant in Manila. Utilize your scientific background to coordinate trials, manage documentation, and ensure regulatory compliance. Enjoy competitive benefits while contributing to innovative healthcare advancements in a dyna...

Join ICON plc as a Clinical Budget Analyst in Blue Bell. Develop and analyze pricing strategies for clinical trials, ensuring financial accuracy and cost optimization. This role requires financial analysis expertise and offers competitive benefits including health insurance and retirement planning.

Lead regional pharmacovigilance activities for a global CRO. Oversee drug safety projects, ensure GVP compliance, and enhance safety processes. Requires 7-12 years' industry experience, including 5+ in PV. Offers competitive health insurance and retirement planning.

Join ICON plc as a Senior Medical Writer and shape the future of clinical development. You will lead medical writing strategies for clinical research, producing high-quality protocols, CSRs, and regulatory documents. This role requires 3-5 years of experience in a CRO/pharma setting and expertise...

Join ICON plc as a Clinical Research Associate II in Bratislava. You will monitor clinical trial sites, ensure GCP compliance, and manage data integrity. This role requires 3-6 years of CRA experience, strong site management skills, and 60% travel. We offer competitive health insurance, retiremen...

Lead our clinical trial feasibility strategy in Reading. Develop data-driven country and site plans to optimize patient recruitment and study delivery. Requires 7+ years in clinical research, drug development knowledge, and strong analytical skills. We offer competitive health insurance, retireme...

Lead regulatory submissions and strategy for drug development at a global CRO. This role in Yerevan requires 6+ years of pharma/biotech experience, including CTA/IND/MAA filings. You will provide expert guidance, manage agency interactions, and ensure compliance. We offer competitive benefits inc...

Lead clinical trial operations in Warsaw, ensuring efficiency and regulatory compliance. This pivotal role requires extensive experience in managing clinical operations and strong leadership skills. You will drive strategic planning, mentor teams, and contribute to innovative therapies. We offer ...

Join ICON plc, a global healthcare intelligence leader, as a Global Clinical Delivery Manager in Sofia. Utilize your 5+ years of clinical research experience and project management skills to coordinate international trials from setup to archival. You will ensure study delivery to time, cost, and ...

Join ICON plc as a Senior Clinical Research Associate specializing in ophthalmology. Oversee clinical trials in the Southeast US, ensuring protocol adherence and data integrity. This role requires complex ophthalmology monitoring experience, particularly in retinal disorders. We offer competitive...