iconplc - Canada, IT - Administration

Senior CRA opportunity in Montreal, Canada, with ICON Plc, specializing in Medical Device and Cardiology trials. You will oversee site monitoring, ensure GCP and regulatory compliance, and manage multiple projects. Requires a Bachelor’s in a scientific field, extensive CRA experience, and strong ...

Join ICON as a Senior CRA in Montreal, Canada, and lead Oncology study monitoring in a sponsor-dedicated role. Leverage your ICH-GCP expertise and medical/science degree to ensure patient safety and data quality. Enjoy 60% travel, competitive benefits including health insurance and retirement pla...

Join ICON plc as a Clinical Research Associate in Montreal, Canada. Monitor multi-therapeutic area studies in a sponsor-dedicated program, focusing on Oncology. Leverage your ICH-GCP expertise and medical knowledge to ensure patient safety and data quality. Enjoy competitive benefits, including h...

Join ICON plc as an **Evidence Delivery Specialist** in Burlington, Canada. You will ensure inspection-readiness by managing TMF/Master File QC, customizing Expected Document Lists, and collaborating with CROs. Ideal for candidates with a Bachelor’s in life sciences, GCP/ICH knowledge, and strong...

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, 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, 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 as a Senior Clinical Research Associate in Burlington, Canada. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Requires oncology monitoring experience and 60% travel. Enjoy health insurance, competitive retirement plans, and a supp...