iconplc

Join ICON plc as a Medical Research Associate/Phlebotomist in San Antonio. You will support clinical trial execution, data collection, and analysis in a vital role. The position requires a medical certification and strong organizational skills. This Sunday-Wednesday schedule includes comprehensiv...

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...