Regulatory Affairs Consultant

Global Labeling Strategy Lead (Contract)

While professional experience and qualifications are key for this role, make sure to check you have the preferable soft skills before applying if required.

Global Pharmaceutical Company

EST timezone (remote) - US-based

Full-time | 6‑month contract

Competitive hourly rate

Start: ASAP

The Opportunity

A global pharmaceutical organisation is seeking an experienced, senior labelling leader to take end‑to‑end ownership of global product labelling across a defined portfolio.

This is a hands‑on leadership role with genuine accountability, not a support- or execution-only position. You will serve as the global steward for core and major‑market labelling , translating data into claims, guiding lifecycle decisions, and balancing regulatory risk with commercial objectives.

Key Responsibilities

Global Labelling Ownership

• Own and maintain global Core Data Sheets (CCDS) and associated patient information
• Lead translation of global data into major‑market labels (e.g. US PI, EU SmPC)
• Manage global vs local deviations and support Health Authority interactions
• Lead complex labelling updates across the product lifecycle

Strategy & Lifecycle Input

• Develop and maintain Target Product Labelling (TPL) to support development and regulatory positioning
• Conduct competitive labelling analyses and regulatory precedent assessments
• Provide labelling xhqgsiq input to global regulatory strategy and major submissions

Candidate Profile

Experience

• 7–10+ years’ experience in Regulatory Affairs with significant global labelling responsibility
• Proven ownership of CCDS and major‑market labels (US and EU)
• Experience supporting regulatory submissions in key markets
• Strong background in TPL development and lifecycle labelling strategy