iconplc - IT - Administration

Join ICON plc in Seoul as a Study Start Up Associate I and help shape the future of clinical development. You will facilitate clinical trial initiation, ensure regulatory compliance, and prepare key submissions like INDs. This role requires a life sciences degree, strong organizational skills, an...

Lead global clinical trials from Seoul with ICON, a top CRO. Utilize your 10+ years of trial management expertise to oversee budgets, drive enrollment, and mentor CRAs. This senior role offers competitive health insurance, retirement planning, and a chance to shape the future of clinical developm...

Join ICON as a Clinical Research Associate II in Seoul, South Korea. Leverage 2+ years of CRA experience and ICH-GCP expertise to design and monitor clinical trials, ensuring data integrity and patient safety. Enjoy extensive travel (60%), competitive benefits, and global support. Advance innovat...

Join ICON as a Sr. TMF Specialist in Raleigh, NC, and ensure clinical trial document accuracy. Leverage 2+ years of TMF experience and a life sciences degree to manage document integrity, conduct audits, and support cross-functional teams. Enjoy benefits like health insurance, retirement planning...

Seeking a Clinical Study Lead in Boston, Basking Ridge, or Philadelphia. Leverage 5+ years of experience, including 3 years in management, to oversee CROs and vendors. Ensure protocol adherence, budget timelines, and strong site relationships. Enjoy competitive benefits, health insurance, and ret...

Senior CTA opportunity at ICON in the United States. Ensure clinical trial site compliance with GCP and regulatory standards. Requires a Bachelor’s in life sciences or clinical research, plus strong site management and analytical skills. Benefits include health insurance, retirement plans, life a...

Join ICON Plc as a Clinical Research Associate and oversee clinical trials across multiple US locations. Leverage your expertise in GCP, site management, and regulatory compliance to ensure data integrity and quality. This role requires a Bachelor’s in a scientific field, 60% travel, and strong p...

Join ICON plc as a Contracts Lead Investigator in Mexico City. You will review, negotiate, and manage clinical trial and vendor contracts, ensuring regulatory compliance. The role requires 2+ years of contract management experience, preferably in pharma or clinical research. We offer competitive ...

Lead Clinical Research Associate (CRA) specializing in Ophthalmology at ICON plc. Lead site management, mentor CRAs, and ensure ICH-GCP compliance across complex trials in the United States. Requires a life sciences degree and extensive CRO experience. Enjoy competitive benefits including health ...

ICON seeks a Clinical Research Associate II in Nanjing, China, to design and analyze clinical trials, ensuring protocol compliance and patient safety. Requires a Bachelor’s in science/healthcare, 2+ years CRA experience, and ICH-GCP knowledge. You will conduct site visits, manage data integrity, ...

Join ICON plc as a Site Management Associate II with French in Warsaw. Support clinical trial site management, ensuring GCP compliance and protocol adherence. Requires a Bachelor’s in life sciences, clinical research experience, and fluency in English and French. Enjoy benefits like annual leave,...

Join ICON plc as a Clinical Research Associate II in the United States. You will monitor clinical trial sites, ensure protocol/GCP compliance, and contribute to advancing innovative therapies. This role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive h...