Regulatory Medical Writing Lead — Hybrid

Johnson & Johnson Innovation; Antwerpen; Hybride; EUR 69 000 - 120 000; Plein temps

Résumé du poste

Johnson & Johnson seeks a Manager, Regulatory Medical Writing to support across therapeutic areas within IDAR. You will lead writing projects and coordinate cross-functional teams, ensuring timely regulatory submissions.

The role is hybrid (3 days onsite weekly) and open across Beerse/Leiden/Neuss/Paris/BeBeerse/Horsham, with global postings. Requires 8+ years in pharma writing and fluent English.

Qualifications

• University/college degree required in a scientific field.
• Masters or PhD preferred for advanced regulatory work.
• Fluency in English with strong written and oral communication.

Responsabilités

• Preparing and finalizing all types of clinical documents.
• Leading in a team environment with independence and steering content strategy.
• Guiding cross-functional teams on processes and best practices.
• Coaching junior staff and overseeing contractors supporting projects.
• Interacting with senior colleagues to strengthen coordination.

Connaissances

Medical Writing

Regulatory Writing

Submission Management

English fluency

Project management

Time management

Cross-functional collaboration

Formation

University/college degree required

Masters or PhD preferred

Description du poste

Johnson & Johnson seeks a Manager, Regulatory Medical Writing to support across therapeutic areas within IDAR. You will lead writing projects and coordinate cross-functional teams, ensuring timely regulatory submissions.

The role is hybrid (3 days onsite weekly) and open across Beerse/Leiden/Neuss/Paris/BeBeerse/Horsham, with global postings. Requires 8+ years in pharma writing and fluent English.