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Regulatory Affairs Officer/Associate Director

IQVIA

SingaporeFull-timeOn-site

Posted 18 Jun 2026

About this role

Prepares and reviews regulatory submissions to support clinical trials and marketing authorizations for internal and external clients. Acts as a Regulatory Team Leader or Project Manager, overseeing technical documentation and managing project budgets. Requires a Bachelor's or Master's degree in Life Sciences or a related discipline. Candidates must demonstrate comprehensive regulatory expertise, strong negotiating skills, and the ability to manage multiple projects independently.

What they're looking for

Regulatory SubmissionsTechnical WritingProject ManagementBudget ManagementClient Relationship ManagementSOP DevelopmentNegotiationMS Office

Frequently asked questions

What does a Regulatory Affairs Officer/Associate Director at IQVIA do?

Prepares and reviews regulatory submissions to support clinical trials and marketing authorizations for internal and external clients. Acts as a Regulatory Team Leader or Project Manager, overseeing technical documentation and managing project budgets. Requires a Bachelor's or Master's degree in Lif…

What skills does this Regulatory Affairs Officer/Associate Director role need?

Key skills for this role include Regulatory Submissions, Technical Writing, Project Management, Budget Management, Client Relationship Management, SOP Development.

How much does a Regulatory Affairs Officer/Associate Director at IQVIA pay?

The employer did not list a salary for this role. Most similar Singapore roles publish their band on the job page.

Is this Regulatory Affairs Officer/Associate Director role remote, hybrid, or on-site?

This role is on-site, based in Singapore.

How do I apply for this Regulatory Affairs Officer/Associate Director role?

You can apply directly on IQVIA's careers page. ApplyLah can tailor your résumé and cover letter to this exact role in seconds first.