Regulatory Medical Writer - Clinical & Submissions Expert

Compassell; Paris; Híbrido; EUR 74.000 - 100.000; A tiempo parcial

Descripción de la vacante

Quanta, based in Paris, is seeking a Regulatory Medical Writer for a Paris-based role. The position involves preparing regulatory and clinical study documents, including investigator brochures, CSRs and protocols, for regulatory submissions.

Ideal candidates will have a post‑grad science degree, fluent English, and experience with marketing authorization processes. This temporary opportunity may require collaboration with health authorities and cross‑functional teams.

Formación

• Post‑grad Science degree required.
• Fluent in English.
• Experience with marketing authorization applications is a plus.

Responsabilidades

• Medical writing of regulatory and clinical study documentation, including IBs, CSRs and protocols.
• Prepare regulatory responses to health authorities.
• Assist in preparation of marketing authorization applications.

Conocimientos

Medical writing

Regulatory writing

Regulatory submissions

Educación

Post‑grad Science degree

Descripción del empleo

Quanta, based in Paris, is seeking a Regulatory Medical Writer for a Paris-based role. The position involves preparing regulatory and clinical study documents, including investigator brochures, CSRs and protocols, for regulatory submissions.

Ideal candidates will have a post‑grad science degree, fluent English, and experience with marketing authorization processes. This temporary opportunity may require collaboration with health authorities and cross‑functional teams.