Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
JobTailor Logo

See all jobs on JobTailor

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Novo Nordisk

Clinical Trials Administrator

Novo Nordisk

Clinical Trial Administrator ensuring smooth execution of clinical trials at Novo Nordisk. Coordinating essential operational activities while maintaining quality and compliance standards.

Posted 5/7/2026contractSeoul • 🇰🇷 South KoreaJuniorWebsite

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Providing comprehensive administrative and operational support across all clinical trial phases, ensuring efficient and compliant study execution
  • Managing trial documentation in the Novo Nordisk Investigator Portal, including set-up, maintenance, and archiving in the (e)TMF and Investigator Site Files
  • Coordinating clinical supply and equipment activities at the country level, including ordering, handling, import processes, and inventory tracking
  • Supporting regulatory submissions by preparing, translating, and submitting documents to Regulatory Authorities and Ethics Committees
  • Facilitating site activation activities, including 'Green Light' checks and drug release documentation
  • Coordinating meeting logistics and follow-ups for local study team meetings, and supporting the preparation of Investigator Meetings
  • Liaising with Vendor Managers and Payment Specialists to facilitate contracting and site payment activities
  • Ensuring cross-functional collaboration and clear communication with internal and external stakeholders, including clinical sites

Requirements

What you’ll need
  • A Bachelor's degree in life sciences or a related field
  • At least 1 year of Clinical Trial Administrator experience in the pharmaceutical industry or Clinical Research Organisation (CRO) is highly preferred
  • Strong organizational and coordination skills with the ability to manage multiple priorities and deadlines
  • Knowledge of ICH-GCP guidelines, regulatory requirements, and clinical trial processes
  • Excellent communication and stakeholder management skills, with the ability to collaborate effectively across functions and cultures
  • Meticulous attention to detail and a commitment to quality and compliance
  • Proficiency in English, both written and spoken.

Benefits

Comp & perks
  • Competitive salary
  • Health insurance
  • Paid time off
  • Professional development opportunities
  • Flexible working arrangements

ATS Keywords

✓ Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
clinical trial administrationregulatory submissionstrial documentation managementinventory trackingsite activation activitiesdocument preparationcompliance managementdata archivingproject coordinationmultitasking
Soft Skills
organizational skillscommunication skillsstakeholder managementattention to detailcollaborationtime managementproblem-solvingadaptabilityinterpersonal skillsleadership