1,723 medical writing jobs at 786 companies in United States
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Senior Director, Medical Writing
Waltham or Boston
$219k-$274k/yrHybridFull Time
Zenas BioPharmaNASDAQ: ZBIO: Develops transformative therapies for patients with autoimmune diseases.
12+ YOEBachelor’s degree in a scientific discipline, 12+ years of medical writing experience, team leadership for global regulatory submissions, and expertise in drug development, clinical research, biostatistics, regulatory requirements, and medical terminology.
Microsoft Word, Microsoft Outlook, Microsoft Excel, Microsoft PowerPoint, Adobe Acrobat, electronic document management systems, document templates, project management tools, reference management tools
SAB BiotherapeuticsNASDAQ: SABS: Developing human antibody-based immunotherapies using a bovine platform.
10+ YOE10+ years medical writing in biotech/pharma; advanced degree in Immunology or related discipline; led BLA/MAA submissions; strong regulatory and cross-functional leadership.
ICH guidelines, CTD/eCTD, FDA/EMA regulatory requirements
AlkermesNASDAQ: ALKS: Develops medicines for psychiatric and neurological disorders.
10+ YOE2+ MgmtDoctorate in a relevant discipline, 10+ years medical writing/clinical research experience, 2+ years people management preferred; experience with regulatory submissions (NDA/BLA/MAA, IND); strong project leadership and communication skills.
Travere TherapeuticsNASDAQ: TVTX: Developing and selling therapies for rare kidney diseases.
7+ YOE7+ years medical/regulatory writing experience in biotech/pharma/CRO; Bachelor's in life/medical/technical sciences required (advanced degree preferred); expert scientific writing; knowledge of FDA/EMA/ICH; Microsoft Office and Veeva proficiency.
Microsoft Office, Veeva platforms, electronic document management systems
Nektar TherapeuticsNASDAQ: NKTR: Develops polymer-based medicines for autoimmune and inflammatory diseases.
15+ YOE12+ Mgmt15+ years medical writing experience, 10+ years writing management, 12+ years supervisory experience; Bachelor's/Master's in life sciences (PhD preferred); expertise with FDA/ICH/CTD, clinical protocols, CSRs, IND/NDA; strong writing, analytical, and leadership skills.
Omnicia, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook
UBC: Providing clinical and commercialization services for the biopharmaceutical industry.
10+ YOEMaster's/PhD preferred,10+ years industry experience with ≥8 years regulatory writing,leadership of medical writing teams,advanced Microsoft Word and Adobe Pro skills,knowledge of clinical trials and REMS preferred.
Allschwil or Beerse or High Wycombe or Leiden or Spring House or Toronto
$117k-$201k/yrHybridFull Time
Johnson & JohnsonNYSE: JNJ: Provides pharmaceutical products and medical technology healthcare solutions.
8+ YOE2+ MgmtUniversity degree required (Masters/PhD preferred); 8+ years pharmaceutical/scientific experience with ≥6 years medical writing and ≥2 years people management; strong regulatory and ICH knowledge and communication skills.
BiogenNASDAQ: BIIB: Develops therapies for neurological and neurodegenerative diseases.
12+ YOEBSc with 12 years or advanced degree with 7 years in medical writing; global regulatory submissions, eCTD, ICH/FDA/EMA requirements, document leadership, project management, MS Word, Veeva, and SharePoint.
Agomab TherapeuticsNASDAQ: AGMB: Developing therapies to restore organ function in fibrotic diseases
15+ YOE15+ years regulatory medical writing experience with independent authorship of Phase 1–3 documents; BS required and advanced degree preferred; deep CTD/ICH knowledge; AI tool experience; CRO management and cross-functional collaboration.
Spring House or High Wycombe or Leiden or Beerse or Allschwil or Toronto
$117k-$201k/yrHybridFull Time
Johnson & JohnsonNYSE: JNJ: Develops and manufactures pharmaceutical drugs and medical devices.
8+ YOE2+ MgmtUniversity degree required (Masters/PhD preferred). 8+ years pharmaceutical/scientific experience, 6+ years medical writing experience, 2 years people management; strong written/oral communication, project leadership, and knowledge of regulatory guidance (ICH).
Acadia PharmaceuticalsNASDAQ: ACAD: Develops and sells medicines for neurological and rare diseases.
5+ YOEMaster’s degree in a related field and 5 years of science and medical writing experience focused on clinical and regulatory documents; pharmaceutical writing certification preferred.
Merck KGaAFrankfurt Stock Exchange: MRK: Develops pharmaceutical, life science, and electronics technologies.
12+ YOE5+ MgmtMaster’s or PhD in a scientific or writing discipline, 12+ years of pharmaceutical or biotech medical writing experience, and 5+ years managing large teams in global matrixed organizations.
Merck KGaA, Darmstadt, GermanyFrankfurt Stock Exchange: MRK: A science and technology in healthcare, life sciences, and electronics.
12+ YOE5+ MgmtRequires a master's or PhD in a scientific or writing discipline, 12+ years of pharmaceutical or biotech medical writing experience, and 5+ years managing large global medical writing teams.
Kyverna TherapeuticsNASDAQ: KYTX: Developing cell therapies for patients with autoimmune diseases.
12+ YOEAdvanced life sciences, pharmacy, or medicine degree preferred; 12+ years of progressive medical writing experience, significant leadership, global regulatory submission expertise, and strong executive communication skills.
Zimmer BiometNYSE: ZBH: Manufactures orthopedic implants and robotic surgical systems.
2+ YOEAuthors regulatory clinical documents, executes literature and National Joint Registry analyses, ensures traceability and compliance; requires relevant degree or equivalent experience and strong scientific writing skills.
Rapport TherapeuticsNASDAQ: RAPP: Developing precision medicines for neurological and psychiatric disorders.
8+ YOERequires 8+ years of biopharmaceutical medical writing experience, late-phase clinical program leadership, regulatory knowledge, AI-tool experience, advanced communication, stakeholder management, and project leadership skills.
Artiva BiotherapeuticsNASDAQ: ARTV: Develops allogeneic natural killer cell-based therapies for various diseases.
4+ YOEBachelor's required (advanced degree preferred), 4+ years preparing clinical/regulatory documents, working knowledge of ICH/GCP and global regulatory expectations, experience with cell/gene/biologics preferred, strong writing and project management skills.
Annexon BiosciencesNASDAQ: ANNX: Develops therapies for complement-mediated neuroinflammatory and autoimmune diseases.
10+ YOE10+ years scientific/medical/technical writing experience, degree in a scientific discipline, experience producing clinical and regulatory documents, ability to interpret data, lead teams, build writing infrastructure, and collaborate cross-functionally.
Microsoft Office, Adobe, Microsoft SharePoint, GraphPad, Tableau, Spotfire
Faro Health: Software platform for clinical trial protocol design and orchestration.
7+ YOE7+ years of medical writing experience in pharmaceutical, biotechnology, or CRO settings; protocol expertise; AI and LLM tool experience; stakeholder leadership; and a bachelor's degree in life, health, or related sciences.