Overview

Voisin Consulting Life Sciences (VCLS) is hiring experienced Regulatory Affairs professionals (Manager to Director level) with deep expertise in Accelerated Market Access (AMA) and Clinical Trial Applications (CTA). If you have experience interfacing with the FDA, this is a strong asset. Location: Global / Remote / Flexible. We are seeking individuals with a track record in AMA and CTA procedures and the ability to interface with regulatory authorities to support development programs.

Responsibilities

• Lead regulatory strategy and execution across development stages
• Provide regulatory guidance for AMA and CTA processes
• Collaborate with cross-functional teams to prepare and submit regulatory submissions
• Engage with regulatory authorities as needed to advance programs

Qualifications

• Regulatory Affairs professionals with 5+ years of experience
• Strong track record in AMA and CTA procedures
• Ability to lead regulatory strategy and execution across development stages
• FDA experience is a strong asset
• Excellent communication skills and a collaborative, proactive mindset

What We Offer

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

Seniority level

• Mid-Senior level

Employment type

• Contract

Job function

• Other

Industries

• IT Services and IT Consulting