iconplc - Remote work

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...

Join ICON Plc in Warsaw as a Senior Clinical Research Associate. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Utilize your 3+ years of CRA experience and site management expertise in this travel-intensive role. We offer competitive health ins...

Join ICON plc as a Clinical Research Associate II in Utrecht. You will monitor clinical trial sites, ensure protocol/GCP compliance, and manage data integrity. Requires 2+ years CRA experience, fluency in Dutch/English, and 60% travel. We offer competitive health insurance and retirement plans.

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

Join ICON plc as a Senior Clinical Research Associate in Oncology. Based in Los Angeles, you will oversee clinical trials, ensuring protocol adherence and data integrity. This role requires 5+ years of CRA experience with oncology monitoring and 60% travel. We offer competitive health insurance a...

Join ICON plc as a Senior Clinical Research Associate in Frankfurt. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Requires extensive CRA experience, fluency in English and German, and 60% travel. Enjoy competitive benefits including health ins...