6 documentation writer jobs at 5 companies in Willingboro, NJ
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Specifications Writer
Conshohocken, Pennsylvania, United States
HybridFull Time
5+ YOE5+ years in construction documentation and technical specifications writing; knowledge of CSI MasterFormat, specification development, technical writing, and ability to support multiple projects and teams.
BSD SpecLink, CSI MasterFormat, FGI, NFPA, ADA
2mo
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Medical Writer
Redmond or Princeton
$80k-$130k/yr OnsiteFull Time
1+ YOEMaster's in life sciences or 3–4 years medical writing experience (PhD with 1+ year acceptable). Requires excellent writing, knowledge of FDA/ICH, clinical data interpretation, and experience with protocols/CSRs/major regulatory documents.
1w
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Senior Medical Writer
Princeton, New Jersey, United States
$120k/yr RemoteFull Time
Synterex: Clinical consulting firm providing regulatory documentation and medical writing.
5+ YOERequires 5+ years of medical writing experience in CRO, biotech, or pharmaceutical settings, a relevant bachelor's degree or higher, regulatory document expertise, Microsoft applications proficiency, and strong communication skills.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook
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Medical Writer Project Director
Iselin, New Jersey, United States
$150k-$180k/yr HybridFull Time
Lead and manage external medical writing consultants, quality-check clinical and regulatory documents, partner with product and clients, and contribute to service strategy; requires clinical/regulatory experience, people management, and comfort with AI.
AuroraPrime, Large Language Models (LLMs), Generative AI
2w
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EG-140 - Regulatory Affairs / Medical Writing
Princeton, New Jersey, United States
$171k-$207k/yr OnsiteFull Time
10+ YOEAdvanced scientific degree or equivalent experience, ~10 years regulatory documentation experience, expert writing skills for regulatory submissions, knowledge of global drug development, document management and publishing processes.
2mo
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Senior Director, Regulatory Science Communication
South San Francisco or Princeton
$248k-$310k/yr HybridFull Time
10+ YOE10+ years in regulatory affairs/writing or scientific communication supporting global submissions; advanced degree preferred; experience with eCTD content, briefing documents, protocols, CSRs, health authority interactions, GxP and inspection readiness; leadership of writers/vendors.