Key Responsibilities

• Develop CMC regulatory strategies for early phase clinical trials
• Prepare and review CMC documentation for CTA and IMPD submissions

• Support IND submission documentation where required
• Ensure compliance with EMA, ICH, and French regulatory requirements
• Collaborate with CRO project teams, manufacturing partners, and sponsors
• Support regulatory authority responses and submission lifecycle management

Requirements

• Experience in CMC Regulatory within pharmaceutical, biotech, or CRO environments
• Strong knowledge of EU and French regulatory frameworks
• Experience preparing CTA, IMPD, or IND documentation
• Knowledge of early phase clinical development

Contract Details

• Freelance / Consultant Position
• Location: France (Fully remote)
• Sector: Clinical Research / Early Phase CRO

Apply now to join an early phase CRO supporting innovative clinical development programmes.

The post Freelance CMC Regulatory – Early Phase CRO – France appeared first on Duchesse Recruitment.

This permanent, home-based position in France, Germany or UK offers an exciting opportunity to lead meaningful clinical studies, collaborate with global teams, and contribute to advancements in medical technology.

What we’re looking for:

• Minimum 5 years’ experience in clinical project management.
• Background in the medical device or life sciences sector.
• Strong knowledge of ICH-GCP and local regulations.
• Fluent in French and English, with excellent communication and leadership skills.

This role combines flexibility, impact, and growth — ideal for someone ready to take their next step in clinical research.

Apply now and let’s move your career forward together.

The post Clinical Project Manager – France, UK, Germany (Home-Based, Permanent) appeared first on Duchesse Recruitment.