Senior Medical Writer / Principal Medical Writer

Precision Medicine Group

. Lead the development of high-quality and on-time clinical study documents .

Posted 9/30/2026full-timeRemote • SlovakiaSenior💰 $100,600 - $182,600 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in developing high-quality clinical study documents in compliance with regulatory guidelines, including ICH, FDA, and GCP. Proficient in managing document workflows and collaborating with cross-functional teams to ensure timely completion of writing assignments.

Highest-signal resume keywords

Clinical Study Document DevelopmentRegulatory Compliance (ICH, FDA, GCP)Medical Writing ExpertiseDocument ManagementProficiency in Microsoft Office Suite

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study ProtocolsIBsICF TemplatesDSURsCSRsCSR Patient NarrativesECTD RequirementsLiterature-Based ResearchAttention to DetailWriting Assignments

Soft Skills

Clear CommunicationAbility to Work in Fast-Paced EnvironmentCollaboration

Tools & Technologies

Microsoft WindowsMicrosoft TeamsMicrosoft WordMicrosoft ExcelAdobe AcrobatMicrosoft PowerPoint

Industry Keywords

Clinical Trial Transparency RequirementsEudraCTCT.govSOPsMedical Writing Processes

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Lead the development of high-quality and on-time clinical study documents
Plan, write, edit, format, and perform QC review of clinical documents including clinical study protocols, IBs, ICF templates, DSURs, CSRs, and CSR patient narratives
Develop documents in compliance with Precision MW Style Guide, Precision SOPs, applicable regulatory guidelines (ICH, FDA, GCP), and eCTD requirements
Manage documents from template to final approved version in collaboration with sponsors, external vendors, and internal Precision project teams/departments
Independently formulate key messages from clinical study data
Author complex content using knowledge, skills, and process understanding
Communicate clearly and concisely with internal and client teams
Contribute to developing and maintaining medical writing processes, SOPs, templates, and work instructions
Perform literature-based research to support writing activities
Perform other duties as assigned

Requirements

What you’ll need

BS degree or equivalent in a scientific or medical discipline with relevant writing expertise
5+ years of experience as a Sr. Medical Writer in the sponsor and/or CRO setting or 7+ years of experience as a Principal Medical Writer
Proficiency with Microsoft Windows, Teams, Word, Excel, Adobe Acrobat, and PowerPoint
Clear understanding of applicable regulations (eg, ICH, FDA, GCP), clinical trial transparency requirements (ie, EudraCT, CT.gov), and eCTD requirements for all phases of development
Impeccable attention to detail and ability to complete writing assignments in a timely manner
Ability to work effectively in a fast-paced environment with multiple high-priority projects with no instruction on routine work and minimal instruction on new assignments
Candidates must be legally authorized to work in the country of employment without employer sponsorship.