Regulatory Submissions Specialist

IQVIA Inc; Tandil; On-site; ARS 92,724,000 - 139,086,000; Full time

Job summary

IQVIA Inc. seeks an Regulatory Affairs professional to prepare and review regulatory submissions supporting clinical trials and marketing authorizations. You will participate in small projects under supervision and collaborate with senior staff to ensure timely delivery.

The role requires 2–3 years in Regulatory Affairs, strong English skills, and knowledge of Chemistry, Manufacturing & Controls, and related guidelines. A Master’s degree is a plus and MS Office proficiency is expected.

Qualifications

• Bachelor's degree in lifescience or related field.
• Master's degree a plus.
• 2–3 years regulatory affairs experience.
• Fluent English (writing, speaking, reading).
• Knowledge of R&D processes and related guidelines.

Responsibilities

• Prepare/review regulatory submissions documents.
• Act as Regulatory Team Member on small projects under guidance.
• Track timelines and manage day-to-day workload.
• Prepare slides/background material for small business meetings.
• Possibly deliver trainings.

Skills

Regulatory knowledge

Project coordination

Interpersonal communication

MS Office

English fluency

Self-motivation

Ability to handle multiple projects

SOP adherence

Education

Bachelor's Degree in Lifescience or related

Master's Degree in Lifescience (plus)

Tools

Microsoft Office

Job description

IQVIA Inc. seeks an Regulatory Affairs professional to prepare and review regulatory submissions supporting clinical trials and marketing authorizations. You will participate in small projects under supervision and collaborate with senior staff to ensure timely delivery.

The role requires 2–3 years in Regulatory Affairs, strong English skills, and knowledge of Chemistry, Manufacturing & Controls, and related guidelines. A Master’s degree is a plus and MS Office proficiency is expected.