Clinical Trials Job at Novo Nordisk, Seoul | Life Sciences | Apply Now
Stepping into the clinical research industry requires precision, organization, and a passion for patient health. If you are looking for a highly strategic Clinical Trials Job in Seoul, this Clinical Trial Administrator (CTA) role at Novo Nordisk is an exceptional opportunity. It is a highly desirable Life Sciences Job for professionals eager to accelerate their Novo Nordisk career by gaining hands-on experience with top-tier global clinical pipelines.
- Job Position: Clinical Trials Administrator (1year 2months)
- Category:Â Clinical Development
- Location: Seoul, Seoul, KR
About the Company
For over 100 years, Novo Nordisk has been unwavering in its commitment to defeating serious chronic diseases. Joining their Global Research & Development unit in Seoul means aligning your Novo Nordisk career with a mission to help millions of people live healthier lives. Within the Clinical Development Center (CDC), you will be part of a team that combines human data, AI tools, and bold scientific ideas to bring transformative therapies from development into the hands of patients. For anyone seeking a meaningful Life Sciences Job, this environment fosters diverse thinking, operational excellence, and lasting, generational impact.
Key Responsibilities
As a CTA, you are the operational engine ensuring that a Clinical Trials Job transitions smoothly from the initial planning phases all the way to final reporting. You will work closely with local study teams to coordinate essential activities while maintaining the highest standards of quality.
- Documentation Mastery: Manage essential trial documentation within the Novo Nordisk Investigator Portal. You will oversee the setup, maintenance, and archiving of the electronic Trial Master File (eTMF) and Investigator Site Files, ensuring audit readiness.
- Site & Supply Coordination: Drive site activation activities, including critical ‘Green Light’ checks and drug release documentation. You will also coordinate clinical supply and equipment at the country level, handling ordering, import processes, and inventory tracking.
- Regulatory Support: Support the clinical pipeline by preparing, translating, and submitting vital documents to Regulatory Authorities and local Ethics Committees.
- Logistics & Vendor Liaison: Coordinate follow-ups and logistics for local study team meetings and Investigator Meetings. You will also liaise closely with Vendor Managers and Payment Specialists to facilitate site contracting and payment activities.
Qualifications & Mindset Required For Clinical Trials Job
To succeed in this Clinical Trials Job, you must thrive in a dynamic, highly regulated environment. This particular Life Sciences Job requires a meticulous eye for detail, a collaborative mindset, and a strong understanding of clinical compliance.
- Educational Foundation: A Bachelor’s degree in life sciences or a related field is required to deeply understand the scientific context of the trials you are administering.
- Required Experience: At least 1 year of direct Clinical Trial Administrator experience within the pharmaceutical industry or a Clinical Research Organisation (CRO) is highly preferred to build your Novo Nordisk career at this level.
- Regulatory Knowledge: You must possess a strong working knowledge of ICH-GCP guidelines, local regulatory requirements, and standard clinical trial operational processes.
- Soft Skills & Languages: Excellent organizational, communication, and stakeholder management skills are mandatory. You must be proficient in English (both written and spoken) to collaborate effectively across global functions and cultures.
Logistics & Application Strategy
- Location: Seoul, South Korea.
- Contract Terms: 1 year and 2 months (This role is explicitly opened as a Childbirth & Maternity leave coverage position).
- Application Deadline: Open until filled. Applications are screened on an ongoing basis, so immediate application is highly encouraged to secure your spot in the interview pipeline.
In summary, this Clinical Trial Administrator role is a fantastic opportunity to gain high-level, global pharmaceutical experience. By taking on this Clinical Trials Job, you will become the operational linchpin for innovative therapies entering the South Korean market. If you have the required ICH-GCP knowledge, meticulous organizational skills, and 1+ year of CTA experience, apply today to secure this premier Life Sciences Job and launch a highly impactful Novo Nordisk career.
