Freelance/Contract Regulatory Affairs Project manager - Clinical trial applications (CTA's)
ProPharma(1 month ago)
About this role
A Regulatory Affairs Project role supporting clinical trial applications (CTAs) for a global life-sciences client across the EU. This is a full-time, remote consultant assignment starting January 2026 for at least six months. The role sits within the client's Regulatory Affairs group and focuses on delivering regulatory support for clinical development under EU regulatory frameworks.
Required Skills
- Regulatory Affairs
- Clinical Trials
- Project Management
- Stakeholder Management
- EU Regulations
- Regulatory Submissions
- Project Leadership
- Documentation Management
- Compliance
- Strategic Planning
+1 more
Qualifications
- BSc in Life Sciences
About ProPharma
propharmagroup.comProPharma helps navigate the complexities of drug development and ensure patient health and safety throughout the product lifecycle.
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