Lead Medical Writer — Regulatory Strategy
Allergan
- p AbbVie is seeking a Principal Medical Writer to lead and write clinical and regulatory documents for drug and/or device development. The role involves coordinating document reviews, ensuring quality, and driving timelines with cross-functional teams.
- p The candidate should have 5+ years in bio-pharma, strong communication, and deep knowledge of ICH/GCP guidelines, with experience across US and EU regulatory expectations.
Vacancy posted 3 days ago
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