Senior Medical Writer – FSP

Thermo Fisher Scientific

Medical Writer producing clinical study reports, protocols, and regulatory documents for Thermo Fisher Scientific. Supporting pharmaceutical/CRO projects through scientific writing, quality compliance, and program coordination.

Posted 8/7/2026full-timeRemote • 🇨🇱 ChileSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical writing and regulatory documentation, with strong skills in data interpretation and project management. Proficient in collaborating with diverse teams to ensure compliance and operational excellence in the pharmaceutical industry.

Highest-signal resume keywords

Clinical Study Report AuthoringRegulatory Documentation KnowledgeScientific Writing ExperienceProject Management SkillsAttention to Detail

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Medical WritingData InterpretationGrammatical SkillsProofreading SkillsDocument Management Systems Knowledge

Soft Skills

Effective CommunicationOrganizational SkillsJudgment and Decision-MakingTeam CollaborationAdministrative Skills

Tools & Technologies

ExcelOutlookClient Templates

Industry Keywords

Pharmaceutical IndustryCRO IndustryDrug Development ProcessQuality ComplianceProgram Management

About the role

Key responsibilities & impact

Serve as primary author for routine documents such as clinical study reports and study protocols, and summarize clinical study data
Assist with complex clinical, scientific, and program-level documents, including IBs, INDs, and MAAs
Ensure compliance with quality processes and requirements for assigned documents
Assist in determining best practices, methods, and techniques for optimal results
Assist with program management activities, including developing timelines, budgets, and forecasts
Represent the department at project launch, review, and project team meetings
Collaborate with internal and external clients to support effective communication and operational excellence

Requirements

What you’ll need

Bachelor's degree in a scientific discipline or equivalent relevant formal academic/vocational qualification
2+ years of comparable relevant experience
Experience in the pharmaceutical/CRO industry preferred
Experience in scientific writing advantageous
Solid medical writing, grammatical, editorial, and proofreading skills
Ability to interpret and present complex data accurately and concisely
Effective administrative, organizational, and planning skills with attention to detail and quality
Ability to work independently and effectively within a team
Effective oral and written communication skills
Knowledge of regulatory documentation and the drug development process
Judgment and decision-making skills
Good computer skills and proficiency with client templates
Knowledge of document management systems and relevant applications such as Excel and Outlook
Occasional willingness to drive to site locations and travel domestically and internationally

Benefits

Comp & perks

Collaboration and development as part of the everyday experience
Reasonable accommodation for individuals with disabilities during application, interview, and employment
Equal opportunity employment