iconplc - South Korea, Seoul, IT - Administration

Join ICON Plc as a Clinical Trial Associate in Seoul, South Korea. Support clinical trial execution with 1+ year SC/CRC experience; IIT/SIT CRA experience preferred. This hybrid role (60% office-based in YeoEuiDo, 40% home-based) involves managing access programs, essential documents, budgets, an...

Senior Regulatory Affairs Specialist sought by ICON plc in Seoul, South Korea. Leverage 3+ years of pharmaceutical or medical device experience to ensure compliance and drive successful product registration. This role demands expertise in drug development, national regulations, and strategic regu...

ICON seeks a Clinical Trial Manager in Seoul, South Korea to drive clinical operations and deliver high-quality outcomes. You will manage study timelines, budgets, and compliance while collaborating with cross-functional teams and investigators. Requires a university degree, 3+ years of PMS/RMP C...

Join ICON as a Clinical Research Associate I in Seoul, South Korea. Leverage your oncology experience and ICH-GCP expertise to independently coordinate study setup, monitoring, and documentation. This role requires 60% travel and strong communication skills to build collaborative relationships wi...

ICON seeks a Clinical Research Associate (CRA II) in Seoul, South Korea. You will design and analyze trials, ensure ICH-GCP compliance, and conduct site monitoring visits. Requires a scientific degree and 2+ years of CRA experience with strong organizational skills. Benefits include health insura...

Join ICON plc as a Senior Clinical Research Associate in Seoul. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Utilize your extensive CRA experience and monitoring expertise, with 60% travel. Enjoy competitive health insurance, retirement plann...

Regulatory Affairs Associate needed in Seoul, South Korea. Leverage 3+ years of clinical regulatory experience, including IND submissions and CMC, to drive study start-up activities. Ensure compliance, manage ethics submissions, and safeguard patient welfare through informed consent review. Benef...

Seeking an experienced **Clinical Trial Manager** in **Seoul, South Korea** to lead complex PMS projects. Requires 7+ years of clinical research experience with a proven track record in project leadership and cross-functional team management. You will oversee trial protocols, budgets, and regulat...

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...

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...

Join ICON Strategic Solutions as a Drug Safety Associate in a home-based role in South Korea. Leverage your pharmacovigilance expertise to manage adverse event reporting, safety data entry, and regulatory submissions. Ideal for candidates with 1+ year experience, a life science or healthcare degr...

ICON seeks a Clinical Research Associate II in Seoul, South Korea to design and analyze global oncology trials. Leverage 2+ years of CRA experience and ICH-GCP expertise to ensure protocol compliance and data integrity. Enjoy competitive benefits including health insurance, retirement planning, a...