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Senior Clinical Research Associate sought by ICON plc in Long Beach, US. Lead monitoring, site management, and compliance for global trials. Requires advanced life sciences degree, extensive CRA experience, and 60% travel. Enjoy competitive benefits including health insurance, retirement planning...

Senior CRA opportunity in Lawrence, US, with ICON Plc. Oversee clinical trial activities, ensuring GCP compliance, data integrity, and participant safety. Requires advanced life sciences degree, extensive site management experience, and 60% travel. Benefits include annual leave, health insurance,...

Senior Clinical Research Associate sought by ICON Plc to oversee global trial activities in Kansas City, MO. Requires advanced life sciences degree, extensive CRA experience, and 60% travel. Manage multiple sites, ensure GCP compliance, and drive data integrity. Benefits include health insurance,...

Senior CRA opportunity in Philadelphia with ICON Plc. Manage clinical trial sites, ensure GCP and regulatory compliance, and drive data integrity. Requires a Bachelor's in a scientific field, extensive CRA experience, and strong site management skills. Enjoy competitive benefits including health ...

Senior CRA role at ICON plc in Mexico City. Manage global clinical trials, ensuring protocol compliance, data integrity, and site performance. Requires advanced life sciences degree, extensive CRA experience, and 60% travel. Benefits include health insurance, retirement planning, and global emplo...

Senior CRA opportunity in Seoul, South Korea with ICON Plc. Manage clinical trial activities, ensure GCP compliance, and oversee multiple sites. Requires a Bachelor's in a scientific field, extensive CRA experience, and strong site management skills. Benefit from competitive health insurance, ret...

Seeking an experienced Clinical Trial Manager to lead oncology studies from Seoul, South Korea, in a home-based role with ICON Strategic Solutions. You will drive clinical deliverables, manage cross-functional teams, and ensure regulatory compliance. Requires 2+ years of CTM experience in a globa...

Seeking a skilled Clinical Research Associate II for a home-based role in South Korea with ICON. Leverage 2+ years of CRA experience and ICH-GCP expertise to conduct site monitoring and ensure data integrity. This role requires 60% travel and offers a dynamic environment advancing clinical develo...

Join ICON as a Site Contract Negotiator in Seoul, South Korea. Support the review and negotiation of clinical trial agreements and budgets, ensuring accurate contract execution for timely study start-up. Ideal for candidates with a Bachelor’s degree and initial experience in contracts or clinical...

Senior Project Manager (Laboratory) sought by ICON in Blue Bell, PA. Lead clinical trial design, analyze complex medical data, and oversee lab operations to ensure quality and timeline adherence. Requires 5+ years in clinical labs/trials, 3+ years PM experience, and a life sciences degree. Enjoy ...

Senior Clinical Research Associate sought by ICON, a world-leading healthcare intelligence organization. Lead oncology trial monitoring with 3+ years’ experience, including Phase I/II solid tumor expertise. Manage multiple sites, ensure GCP compliance, and drive data integrity in Blue Bell, PA. E...

Senior Clinical Research Associate opportunity in Raleigh, NC with ICON Plc. Manage and monitor clinical trial sites, ensuring GCP and regulatory compliance. Requires a Bachelor's in a scientific field, extensive CRA experience, and strong site management skills. Benefit from competitive health i...