Senior Medical Writer

Veristat; France; Sur place; EUR 60 000 - 80 000; Plein temps

Résumé du poste

Veristat is seeking a Senior Medical Writer to independently plan and prepare regulatory documents for all phases of product development. You will organize, analyze, and present scientific information in line with ICH and company standards, while collaborating with cross‑functional teams on document production.

Ideal candidates have a minimum of 5 years in medical writing within CRO or pharma settings, with excellent English and strong attention to detail.

Qualifications

• Bachelor’s degree in a science‑related field is required.
• Minimum of 5 years of medical writing experience in CRO or pharma settings.
• Advanced knowledge of ICH and related regulatory guidelines.
• Excellent written English and strong attention to detail.
• Strong interpersonal and communication skills.

Responsabilités

• Independently plans and prepares regulatory documents and medical communications for all phases of product development.
• Organizes, analyzes, interprets, and presents scientific and statistical information per ICH and company standards.
• Collaborates with cross‑functional internal and external document production teams.

Connaissances

Written English

Interpersonal skills

Attention to detail

Formation

Bachelor’s degree in a science-related field

Outils

Microsoft Word

Microsoft Office Suite

Description du poste

Senior Medical Writer

The Senior Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. The primary responsibilities of the position are organizing, analyzing, interpreting, and presenting scientific and statistical information in accordance with International Council for Harmonisation (ICH) and other regulatory guidelines, and individual company document standards. The Senior Medical Writer works under the direction of Medical Writing management and collaborates with cross-functional internal and external document production teams.

Job Description

Senior Medical Writer

The Senior Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. The primary responsibilities of the position are organizing, analyzing, interpreting, and presenting scientific and statistical information in accordance with International Council for Harmonisation (ICH) and other regulatory guidelines, and individual company document standards. The Senior Medical Writer works under the direction of Medical Writing management and collaborates with cross-functional internal and external document production teams.

Make an Impact at Veristat!

• 105+ approved therapies for marketing applications prepared by Veristat
• 480+ oncology projects in the past 5 years
• 350+ rare disease projects delivered in the past 5 years
• Flexible, inclusive culture — 70% remote workforce, 66% women-led teams
• Learn more about our core values here!

What We Look For

• Bachelor’s degree required; science-related field preferred.
• Minimum of 5 years of medical writing experience in a contract research organization or pharmaceutical/biotechnology research setting. Other professional and/or educational experience may contribute toward this minimum requirement, as determined on a case-by-case basis; however, a minimum of 3 years of formal medical writing experience is required.
• Advanced knowledge of ICH and related regulatory guidelines.
• Excellent written English and keen attention to detail.
• Strong interpersonal and communication skills.
• Experience with Microsoft Office Suite is essential, including advanced Microsoft Word proficiency.

Automated Decision Making: All applicants are reviewed by a member of the Veristat Talent Acquisition team; Veristat does not utilize an automated decision-making process.

Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.