iconplc - South Korea, Remote work

Join ICON plc, a global clinical research leader, as a Senior Clinical Research Associate in Seoul, South Korea. You will oversee oncology trial sites, ensuring protocol adherence, data integrity, and GCP compliance. This role requires extensive CRA experience, strong site management skills, and ...

Join ICON plc's dynamic team in Seoul as a Regulatory Affairs Specialist. You will design clinical trials, interpret medical data, and prepare key submissions (CT/IND, MAA/NA). This role requires 2-3 years of pharmaceutical regulatory experience. We offer competitive health insurance, retirement ...

Join ICON's dynamic team as a Study Start-Up Associate II, based in Seoul. You will lead clinical trial initiation, ensuring regulatory compliance with ICH-GCP and local requirements. This home-based role offers competitive health insurance and retirement benefits. Utilize your 2+ years of study ...

Join ICON plc as a Clinical Research Associate II in Seoul, South Korea. This home-based oncology role requires a Bachelor's degree and 2+ years of CRA experience with ICH-GCP knowledge. You will conduct site monitoring, ensure data integrity, and contribute to advancing cancer therapies, with 60...

Join ICON plc in Seoul as a Clinical Research Associate II. You will monitor clinical trial sites, ensure protocol/GCP compliance, and contribute to advancing treatments. This role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. A competitive benefits package supports your...

Join ICON plc as a Senior Clinical Research Associate in Seoul. Oversee global oncology trials, ensuring protocol adherence, data integrity, and GCP compliance. This role requires extensive CRA experience, strong site management skills, and 60% travel. We offer competitive health insurance, retir...

Join ICON plc in Seoul as a Study Start Up Associate II and help shape the future of clinical development. You will lead clinical trial initiation, ensure regulatory compliance, and manage essential documents. This role requires 2+ years of study start-up experience and offers competitive health ...

Lead regulatory submissions and strategy as a home-based Manager in Seoul. Utilize 6+ years of pharmaceutical regulatory experience to guide drug development from CTA to post-approval. Enjoy competitive benefits including health insurance and global support, driving excellence at a world-leading ...