Regulatory Affairs Specialist — Clinical Trials & MA

IQVIA; Buenos Aires; On-site; ARS 114,242,000 - 167,555,000; Full time

Job summary

IQVIA is seeking a Regulatory Affairs professional to prepare and review regulatory submissions for clinical trials and marketing authorization activities. You will support assigned projects and collaborate with clients and senior staff to ensure timely delivery.

The role requires a Bachelor’s in Life Sciences, 2–3 years of regulatory experience, and fluent English. Experience with US/Canada regulatory activities is a plus. Strong communication and organization skills are essential.

Qualifications

• Bachelor's Degree in Lifescience or related discipline.

Responsibilities

• Prepares and/or reviews regulatory submissions documents to support clinical trial and marketing authorization activities.
• Provides regulatory support for assigned projects.
• Acts as Regulatory Team Member on small, straightforward regulatory projects under guidance of senior staff.
• Tracks project timelines and manages day-to-day workload with senior staff.

Education

Bachelor's Degree in Lifescience or related discipline

Job description

IQVIA is seeking a Regulatory Affairs professional to prepare and review regulatory submissions for clinical trials and marketing authorization activities. You will support assigned projects and collaborate with clients and senior staff to ensure timely delivery.

The role requires a Bachelor’s in Life Sciences, 2–3 years of regulatory experience, and fluent English. Experience with US/Canada regulatory activities is a plus. Strong communication and organization skills are essential.