iconplc - IT - Administration

Senior Clinical Research Associate (CRA II) sought for a hybrid role in Bucharest, Romania, specializing in oncology. You will independently monitor clinical trials, ensuring GCP and regulatory compliance across SSVs, SIVs, IMVs, and COVs. Requires 18+ months of on-site monitoring experience, a l...

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...