iconplc - Remote work

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...

Join ICON plc as a Clinical Research Associate II in Prague. You will monitor clinical trial sites, ensure protocol/GCP compliance, and manage data integrity. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We offer competitive health insurance, retire...

Join ICON plc in Seoul 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, ICH-GCP knowledge, and 60% travel. A competitive benefits package supports your...

Join ICON plc as a Senior Clinical Research Associate in Seoul. Oversee global oncology trials, 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, retir...

Join ICON plc in Seoul as a Study Start Up Associate II and help shape the future of clinical development. You will lead clinical trial initiation, ensure regulatory compliance, and manage essential documents. This role requires 2+ years of study start-up experience and offers competitive health ...

Join ICON plc as a Clinical Research Associate in Miami, focusing on start-up activities across multiple therapeutic areas. You will identify and activate trial sites, ensuring compliance with ICH-GCP. This role requires 2-3 years of monitoring experience and offers competitive health insurance a...