19h ago
New

Global Regulatory Lead

FranceFrance·SaclayRemoteFull-timelead
Legal & ComplianceRegulatory
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Quick Summary

Key Responsibilities

Developing and maintaining global regulatory strategies aligned with development and business objectives. Assessing evolving regulatory

Technical Tools
Legal & ComplianceRegulatory

Join Excelya, where Audacity, Care and Energy define who we are and how we work. We believe in creating ambitious solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

To strengthen one of our strategic partnerships, we are looking for a Global Regulatory Lead to drive global regulatory strategies and support the development and registration of innovative products worldwide.

Key responsibilities :

  • Developing and maintaining global regulatory strategies aligned with development and business objectives.
  • Assessing evolving regulatory requirements, competitor landscapes, and regulatory intelligence across major markets.
  • Leading interactions with Health Authorities, including EMA, FDA, PMDA, and other key agencies.
  • Driving regulatory activities related to registrations, lifecycle management, orphan drug designation, and market expansions.
  • Designing and overseeing global submission plans in collaboration with regional regulatory teams and submission management.
  • Acting as a core member of global cross-functional project teams, ensuring alignment between Regulatory Affairs, Clinical Development, Safety, CMC, Market Access, and other stakeholders.
  • Supporting the preparation and maintenance of CTA/IND documentation, CTD modules, briefing books, regulatory Q&A packages, PIP/PSP activities, and other key regulatory deliverables.
  • Leading label development activities and contributing to Company Core Data Sheets (CCDS).
  • Managing regulatory risk assessments and maintaining regulatory risk registers.
  • Supporting registration activities in key markets and contributing to regulatory due diligence and licensing initiatives when required.
  • Evaluating the regulatory impact of quality, efficacy, or safety findings throughout product development.

Requirements

~1 min read

At Excelya, we encourage taking daring steps, so we seek individuals who are ready to grow with our mission and embody our values.

Why join us?

At Excelya, we combine a passion for science with the enthusiasm of teamwork to redefine excellence in healthcare.

Here's what makes us unique:

We are a young and ambitious healthcare company, bringing together 900 Excelyates, driven by the goal of becoming the leading mid-sized CRO in Europe, while offering the best employee experience.

Our "one-stop provider" service model—combining full-service, functional service provider, and consulting—allows you to grow through diverse and stimulating projects. By collaborating with leading experts, you will contribute to the development of scientific, operational, and human knowledge, all in service of improving the patient journey.

Excelling with kindness means evolving in an environment that values ​​your natural talents, encourages boldness, pushes boundaries, and cultivates your potential, so that you can fully contribute to our shared mission.

Location & Eligibility

Where is the job
Saclay, France
Remote within one country

About this job

Posted
Today
Employer
has 36 open jobs on Jobera in 7 countries.

Listing Details

Posted
November 9, 2026
First seen
November 9, 2026
Last seen
November 9, 2026

Posting Health

Days active
0
Repost count
0
Trust Level
76%
Scored at
November 9, 2026

Signal breakdown

freshnesssource trustcontent trustemployer trust

Excelya is an independent partner that serves Biotech, Pharma, and Medical Device organizations with a comprehensive range of full-service CRO, FSP, and Resourcing solutions.

Employees
501-1,000
View company profile
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Global Regulatory Lead