Regulatory Affairs Manager

Lifelancer Ltd; United States; Remote; USD 95,000 - 123,000; Full time

Job summary

IQVIA in Courbevoie, France, is seeking a Regulatory Affairs Manager to oversee country-level regulatory activities for medicinal products on the French market, with a home-based work arrangement.

You will prepare submissions, coordinate with internal and external stakeholders, translate labeling into French, review artwork, and support regulatory maintenance across multiple products, ensuring compliance and timely filings.

Qualifications

• 3+ years of regulatory affairs experience for medicinal products on the French market.
• Experience coordinating regulatory submissions with authorities and stakeholders.
• Knowledge of French pharmaceutical regulation and timelines.

Responsibilities

• Manage country-level regulatory activities for medicinal products in France.
• Prepare and coordinate regulatory submissions, including notifications and variations.
• Lead submission processes with local Health Authorities through to approval.
• Prepare and translate product labeling into French (SmPC, PIL).
• Review artwork and promotional materials in client systems.
• Support regulatory maintenance across multiple products.

Skills

Regulatory affairs

Submission coordination

French market

Communication

Education

Bachelor of Pharmacy or Life Sciences

Tools

MS Office

Regulatory systems

Artwork tools

Job description

Job Title: Regulatory Affairs Manager

Job Location: Courbevoie, France

Job Location Type: Home-based

Job Contract Type: Full time

Job Seniority Level: Shape the future of regulatory excellence at IQVIA

At IQVIA, we work to advance healthcare by helping our clients bring safe, effective medicines to patients. As a Regulatory Affairs Manager, you will play a key role in ensuring compliance and supporting successful product lifecycle management in France. You’ll collaborate with leading global pharmaceutical companies and contribute to high‑quality regulatory outcomes that truly make a difference. This is a fixed-term opportunity for 12 months.

What you will do

• Manage country‑level regulatory activities for medicinal products, ensuring full compliance with local requirements.
• Prepare and coordinate regulatory submissions in partnership with internal and external stakeholders, including notifications, renewals, variations, new applications, and MAH transfers.
• Lead submission processes with local Health Authorities and follow up through approval.
• Prepare and translate product labelling into French (e.g., SmPC, PIL).
• Review and approve artwork and promotional materials in client systems.
• Support regulatory maintenance activities across multiple pharmaceutical products.
• Monitor local pharmaceutical legislation and ensure updates are applied appropriately.

What you need to succeed

• Bachelor of Pharmacy or other Life Sciences degree.
• 3+ years of experience in regulatory affairs for medicinal products on French market, including submission document preparation and coordination.
• Experience within a large regulatory organization, with both centralized and local activities, is an advantage.
• Excellent knowledge of pharmaceutical legislation and regulatory requirements in France.
• Excellent organizational skills, attention to detail, and ability to meet timelines.
• Strong communication skills and a collaborative working style.
• Native French and fluent written and verbal communication skills in English.
• Strong computer skills, including MS Office; experience with regulatory information systems and artwork tools is a plus.

Why join IQVIA

When you join IQVIA, you become part of a global team that is dedicated to driving smarter healthcare for everyone, everywhere. You will collaborate with industry experts, grow your regulatory career through continuous learning, and contribute to meaningful work that supports better patient outcomes. We foster a culture of innovation, teamwork, and shared purpose — and we’re excited to welcome passionate professionals like you.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law.

We appreciate your honesty and professionalism.