IQVIA | Regulatory & Start-Up Specialist – Seoul

Website IQVIA

Discover how an IQVIA Regulatory & StartUp Specialist can help your business in Seoul, South Korea. Learn more about the services provided and how they can benefit your business.

Duties and Responsibilities

  • Ensure accurate completion and maintenance of internal systems, databases, and tracking tools with project-specific information.
  • Review and provide feedback to management on site performance metrics.
  • Review, establish, and agree on project planning and project timelines.
  • Ensure monitoring measures are in place and implement a contingency plan as needed.
  • Inform team members of the completion of regulatory and contractual documents for individual sites.
  • Review, track, and follow up on the progress, approval, and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines.

Q: What Experience is Needed?

A: The ideal candidate should have at least 1 year of experience in the pharmaceutical industry and knowledge of standard operating procedures (SOPs).

Q: What is the Education Qualifications Needed to apply?

A: The job requires a Bachelors degree in a related field and/or an equivalent combination of education and experience in the pharmaceutical industry.

Conclusion: If you have a passion for working in the pharmaceutical industry and have the necessary qualifications and experience, this job opportunity is perfect for you. With a competitive salary and other attractive benefits and perks, you will gain invaluable experience and be part of a team that is making a difference in peoples lives. Dont wait apply today!

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