Medical Writer – Global Clinical Development

Regeneron

. Develop clinical documents including clinical study reports, protocols, informed consent forms, narratives, and investigator brochures .

Posted 10/15/2026full-timeRemote • New York • United StatesJunior💰 $109,900 - $179,300 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in developing clinical documents such as study reports and protocols while ensuring compliance with industry standards and regulations. Strong ability to synthesize complex information into clear written content and collaborate effectively with cross-functional teams.

Highest-signal resume keywords

Clinical Document DevelopmentRegulatory ComplianceScientific WritingMicrosoft WordAdobe Acrobat

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study ReportsProtocolsInformed Consent FormsNarrativesInvestigator BrochuresDocument StrategyDocument TimelinesPeer-Review PracticesElectronic Document Management SystemsStandard Operating Procedures

Soft Skills

Organizational SkillsInterpersonal SkillsCommunication Skills

Tools & Technologies

Microsoft PowerPointAdobe Acrobat

Industry Keywords

Clinical Research ProcessMedical WritingTherapeutic AreasInternal StandardsTemplates

About the role

Key responsibilities & impact

Develop clinical documents including clinical study reports, protocols, informed consent forms, narratives, and investigator brochures
Manage and facilitate document completion with oversight from Medical Writing leads
Lead document activities for a compound when assigned
Drive document development meetings and support timeline execution
Articulate document strategy and document timelines
Identify appropriate stakeholders for content decisions and keep discussions progressing
Synthesize complex discussions into clear, accurate written content
Collaborate with colleagues and help resolve issues while escalating concerns when needed
Support timely, compliant document delivery across therapeutic areas
Collaborate with cross-functional study teams and Medical Writing colleagues

Requirements

What you’ll need

Bachelor’s degree; advanced degree preferred
1 year of relevant experience
Awareness of the clinical research process and applicable regulations and guidelines
Scientific and technical reading, writing, and editing skills
Experience following internal standards, procedures, templates, and peer-review practices
Knowledge of guidelines, templates, and standard operating procedures for Medical Writing documents
Working knowledge of Microsoft Word, Adobe Acrobat, and PowerPoint
Familiarity with electronic document management systems
Strong organizational, interpersonal, and communication skills
Ability to maintain current knowledge of industry standards and complete required training

Benefits

Comp & perks

Annual bonuses or other incentive plans
Equity awards
Pension or retirement benefits
401(k) company match
Health and wellness programs
Fitness centers
Medical, dental, vision, life, and disability insurance benefits
Paid time off
Family support benefits
Reasonable accommodation during the recruitment process where required