Regulatory Medical Writer

Compassell; Paris; Hybrid; EUR 74,000 - 100,000; Part time

Job summary

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.

Qualifications

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

Responsibilities

• 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.

Skills

Medical writing

Regulatory writing

Regulatory submissions

Education

Post‑grad Science degree

Job description

Our global client based in the beautiful city of Paris is now looking for a professional to join their team on a permanent basis.

Features

Exact Job Title: Regulatory Medical Writer

Date Posted: 03/14/2021

Valid Through: 08/02/2021

Employment Type: Temporary

Base Salary: $100,000.00

Hiring Organization: Quanta

Employer Overview: Duties and responsibilities will include the following but not limited to:

• Medical writing of all types of Regulatory and clinical study documentation, including Investigator Brochures, clinical study reports and protocols.
• Preparation of regulatory responses to health  authorities
• Preparation of marketing applications

Education Requirements: Previous Scientific or Medical Writing experience

• Post‑grad Science degree
• Fluent in English 
• Experience in the marketing authorisation applications and regulatory would be advantageous.