Lead Medical Writer, Regulatory – Remote

ThermoFisher Scientific; France; Hybride; EUR 90 000 - 120 000; Plein temps

Résumé du poste

Thermo Fisher Scientific is expanding its Medical Writing FSP team in Europe with a Principal Medical Writer role. This remote position supports a client in the FSP space, focusing on planning, coordination, and delivering high-quality clinical documentation.

You will mentor junior writers and provide strategic guidance on regulatory and industry best practices. Ideal candidates bring 8+ years in medical writing, experience across neurology/immunology/oncology or vaccines, and the ability to

Qualifications

• Bachelor's in a scientific field with experience in medical writing.
• Experience leading complex medical writing projects.
• Regulatory knowledge for submissions and correspondences.
• Mentorship of junior writers and training delivery.

Responsabilités

• Write, edit, and review clinical study reports and protocols.
• Provide senior input on complex documents and training.
• Ensure quality processes and best practices in document development.
• Lead project discussions and collaborate with clients and teams.

Connaissances

Medical writing

Regulatory writing

Project management

Mentoring

Communication

Formation

Bachelor's degree in scientific discipline

Advanced degree preferred

Certifications AMWA EMWA RAC advantageous

Description du poste

Thermo Fisher Scientific is expanding its Medical Writing FSP team in Europe with a Principal Medical Writer role. This remote position supports a client in the FSP space, focusing on planning, coordination, and delivering high-quality clinical documentation.

You will mentor junior writers and provide strategic guidance on regulatory and industry best practices. Ideal candidates bring 8+ years in medical writing, experience across neurology/immunology/oncology or vaccines, and the ability to