Senior Medical Writer

About the role

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.

Responsibilities

• Organizing, analyzing, interpreting, and presenting scientific and statistical information in accordance with ICH and other regulatory guidelines.
• Following individual company document standards.
• Working under the direction of Medical Writing management.
• Collaborating with cross-functional internal and external document production teams.

Requirements

• 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.

Qualifications

• Advanced knowledge of ICH and related regulatory guidelines.

Skills

• 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.

Benefits

• Flexible, inclusive culture.
• 70% remote workforce.
• 66% women‑led teams.
• 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.