EMEA Regulatory Affairs Manager - Remote

Worldwide; France; Remote; EUR 90,000 - 130,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Manager of Regulatory Affairs for the EMEA region with remote work flexibility. You will lead regulatory submissions, coordinate cross‑region activities, and provide expert regulatory guidance to sponsors and internal teams.

The role requires a strong background in regulatory strategy, 5–7 years in pharma/CRO settings, and excellent English communication. A senior, globally oriented leader who can drive complex projects in a fast-paced environment is ideal.

Qualifications

• Proven leadership and organizational management skills.
• Strong planning, strategizing and monitoring abilities.
• Excellent written and verbal communication across diverse teams.

Responsibilities

• Review study budgets, assist in contract negotiations and support business development.
• Coordinate regulatory submissions across EMEA, Asia Pacific and Latin America.
• Provide regulatory expertise and communicate submission status to sponsors and project teams.
• Contribute to preparation of technical documentation like IMPDs and IBs to ensure compliance with ICH GCP and country rules.
• Mentor junior staff and possibly line manage team members as needed.

Skills

Leadership

Regulatory strategy

Project management

Cross-functional communication

Education

Bachelor's degree in Life Sciences

Job description

Worldwide Clinical Trials is seeking a Manager of Regulatory Affairs for the EMEA region with remote work flexibility. You will lead regulatory submissions, coordinate cross‑region activities, and provide expert regulatory guidance to sponsors and internal teams.

The role requires a strong background in regulatory strategy, 5–7 years in pharma/CRO settings, and excellent English communication. A senior, globally oriented leader who can drive complex projects in a fast-paced environment is ideal.