Regulatory Affairs Professionals - Manager to Director

Summary

Join Voisin Consulting Life Sciences (VCLS) and pioneer the future of regulatory science and clinical research. We are seeking experienced Regulatory Affairs professionals at the Manager to Director level with extensive expertise in Accelerated Market Access (AMA) and Clinical Trial Applications (CTA). FDA experience is a plus. VCLS offers meaningful work contributing to innovative health solutions, opportunities for growth and development, and a collaborative culture. We provide flexible contract opportunities, access to a global network of experts, and a dynamic work environment. Continuous professional development and training are also offered.

Requirements

• Possess 5+ years of experience in regulatory affairs
• Demonstrate a strong track record in AMA and CTA procedures
• Exhibit excellent communication skills and a collaborative, proactive mindset

Responsibilities

• Develop regulatory strategies and execute them across various development stages
• Lead and manage regulatory affairs projects
• Interface with regulatory agencies (e.g., FDA)
• Collaborate effectively with cross-functional teams
• Maintain strong communication skills, both written and verbal

Preferred Qualifications

FDA experience is a strong asset

Benefits

• A multitude of flexible contract opportunities
• Access to a global network of regulatory experts
• Dynamic, mission-driven work environment
• Continuous professional development and training