Principal Medical Writer – Clinical Focus

Veristat

Principal Medical Writer preparing regulatory documents and medical communications for Veristat, a clinical research organization accelerating life-changing therapies. Supporting product development through scientific analysis, ICH compliance, and cross-functional document collaboration.

Posted 8/13/2026full-timeRemote • Massachusetts • 🇺🇸 United StatesLead💰 $142,000 - $153,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in medical writing, regulatory document preparation, and adherence to ICH guidelines. Strong ability to analyze and present scientific information while collaborating effectively with cross-functional teams.

Highest-signal resume keywords

Medical Writing ExperienceICH Guidelines KnowledgeRegulatory Document PreparationMicrosoft Office Suite ProficiencyInterpersonal Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Regulatory Document PreparationMedical WritingStatistical AnalysisScientific InterpretationAttention to Detail

Soft Skills

Strong Communication SkillsInterpersonal Skills

Tools & Technologies

Microsoft Office Suite

Industry Keywords

Contract Research OrganizationPharmaceutical ResearchBiotechnology ResearchRegulatory Guidelines

About the role

Key responsibilities & impact

Independently plan and prepare regulatory documents and medical communications supporting all phases of product development
Organize, analyze, interpret, and present scientific and statistical information according to ICH and other regulatory guidelines
Prepare documents in accordance with company document standards
Work under the direction of Medical Writing management
Collaborate with cross-functional internal and external document production teams

Requirements

What you’ll need

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 the minimum experience requirement on a case-by-case basis
Advanced knowledge of ICH and related regulatory guidelines
Excellent written English
Keen attention to detail
Strong interpersonal and communication skills
Experience with Microsoft Office Suite is essential

Benefits

Comp & perks

Remote working
Flexible time off
Paid holidays
Medical insurance
Tuition reimbursement
Retirement plans
Applicable bonus
Inclusive culture
Reasonable accommodations and accessible application experience