iconplc - Remote work

Join ICON plc as a Senior Clinical Associate in Warsaw. Support clinical trial management with a focus on inspection readiness and document management. Requires a Bachelor's degree and 2+ years of CTA experience in Pharma/CRO. We offer competitive benefits including health insurance and retiremen...

Join ICON plc as a Visualization Developer and shape the future of clinical development. Leverage your 4+ years of experience with Python, Spotfire, and clinical data (SDTM) to build advanced analytics solutions. Enjoy a supportive, innovative environment with competitive health insurance and ret...

Join ICON plc as a Clinical Research Associate II in Seoul, South Korea. This home-based oncology role requires a Bachelor's degree and 2+ years of CRA experience with ICH-GCP knowledge. You will conduct site monitoring, ensure data integrity, and contribute to advancing cancer therapies, with 60...

Join ICON plc as a Senior Clinical Research Associate in the cardiovascular medical device space. This role requires deep FDA/ICH-GCP knowledge and strong site management skills for a key cardio/electrophysiology study. Enjoy competitive benefits and the flexibility of multiple US locations while...

Join ICON plc as a Senior Clinical Research Associate in the US, focusing on a cardiovascular medical device study. This role requires deep expertise in FDA/ICH-GCP guidelines and exceptional site management skills. We offer competitive benefits including health insurance and retirement planning,...

Join ICON plc as a Clinical Research Associate II in Toronto/Burlington. You will monitor clinical trial sites, ensure ICH-GCP compliance, and contribute to advancing new therapies. The role requires 2+ years of CRA experience and 60% travel. We offer competitive health insurance, retirement plan...

Join ICON plc as a Senior Clinical Research Associate specializing in Orthopedics across the Western US. You will monitor 4-5 orthopedic device studies, ensuring compliance with FDA/ICH-GCP. This role requires strong site management and problem-solving skills. We offer competitive health insuranc...

Join ICON plc, a global clinical research leader, as a CRA I in Burlington, Canada. Utilize your 2+ years of monitoring experience and ICH-GCP knowledge to conduct site visits and ensure trial excellence. This role offers competitive benefits and involves approximately 60% travel.

Join ICON plc, a global clinical research leader, in Mexico City. As a Clinical Associate, you will support the design and management of clinical trials, advancing innovative therapies. The role requires a Life Sciences degree, clinical research experience, and strong organizational skills. We of...

Join ICON plc in Lisbon as a Clinical Research Associate II. You will monitor clinical trial sites, ensure protocol/GCP compliance, and contribute to advancing treatments. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We offer competitive health insu...

Join ICON plc, a global clinical research leader, as a Senior Clinical Research Associate. This role requires 1-3+ years of monitoring experience, with oncology expertise preferred, and 70% travel. You will ensure trial compliance with ICH-GCP at sites across Canada, supported by comprehensive he...

Join ICON plc, a global clinical research leader, as a Senior CRA/CRA II. This home-based role in Melbourne, Sydney, or Brisbane partners you with a premier Biopharmaceutical company. You will monitor sites, ensure GCP compliance, and manage trials across a vast portfolio. The role requires exten...