Principal Medical Writer – Clinical Focus

Veristat

Posted on: August 13, 2026

Closing: September 12, 2026

Salary: Undisclosed

Position Type: Full Time

Job Description

Job Description:

Overview

The Principal 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 Principal 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!

Join a global team with more than 30 years of expertise accelerating life-changing therapies to patients worldwide.
  • 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 offer:

The estimated hiring range for this role is $142K-153K USD plus applicable bonus. This hiring range is specific to the US and will vary for other regions based upon local market data. Final salary is ultimately decided upon taking into account a wide range of factors, including but not limited to: skills and experience, licensure and certifications, education, specific location and dynamic market data.

Benefits vary by location and may include:
  • Remote working
  • Flexible time off
  • Paid holidays
  • Medical insurance
  • Tuition reimbursement
  • Retirement plans

What we look for:
  • Bachelor's degree required; science-related field preferred.
  • Minimum of 7 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.
  • 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

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.

Veristat

Posted on: August 13, 2026

Closing: September 12, 2026

Salary: Undisclosed

Position Type: Full Time

Career Focus: Medical Writing

This role is part of a curated selection of life science opportunities featured on Xtalks. Employers may request edits or removal here.

Similar Jobs


United States

Medical Writer, Medical Communications

Are you a passionate individual that thrives when building scientific co...

United States

Director, Medical Writing – Market...

PRECISION AQ, the top payer marketing agency, supports global pharmaceut...

United States

Senior Scientific Associate / Senior...

PLEASE NOTE: This role supports clients in the Central Time Zone. Candid...

United States

Senior Medical Writer, Medical Communications

Are you passionate about transforming complex science into meaningful, i...