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Senior Medical Writer

🕒 vor 1 Monat

🇬🇧 Vereinigtes Königreich – Remote

⏰ Vollzeit

🟠 Senior

🏥📝 Medizinischer Autor

🗣️🇺🇸🇬🇧 Englisch erforderlich

Woher diese Stelle stammt

Veröffentlicht auf der Karriereseite von TransPerfect, nicht über eine Jobbörse

Von Remote Rocketship zum ersten Mal gesehen vor 1 Monat

Noch offen auf der Website von TransPerfect. Geprüft vor 4 Stunden.

Logo of TransPerfect

TransPerfect

5001 - 10000 Mitarbeiter

💼 Beratung

⚖️ Rechtswesen

📣 Marketing

Consulting • Legal • Marketing

TransPerfect ist ein globales Sprach- und Technologieunternehmen, das Übersetzungs-, Lokalisierungs-, Dolmetsch- und Inhaltsdienste anbietet, kombiniert mit Software- und KI-gestützten Tools wie der GlobalLink Translation Management Plattform. Es bietet mehrsprachiges Marketing, rechtliche und regulatorische Unterstützung im Bereich Life-Sciences, Contact Center/BPO-Dienste, Multimedia-Lokalisierung sowie Lösungen für die Globalisierung von Webseiten, Software und Apps. TransPerfect bedient große Unternehmen und Fortune-500-Kunden aus dutzenden Branchen und unterstützt Inhalte in über 200 Sprachen.

Beschreibung

• Lead execution of clinical regulatory documents and related project management tasks, including creating, maintaining, and communicating timelines • Coordinate cross-functional client contributors, stakeholders, and internal resources such as quality control and publishing • Ensure document development follows client processes, templates, and instructional documents • Serve as an expert on client document management systems, tools, templates, and procedures • Lead document message development with clients • Interpret data and create shell documents to support authoring • Plan and lead kickoff meetings • Facilitate review-feedback resolution, including planning and leading comment resolution meetings • Follow up with team members to resolve outstanding review feedback • Ensure consistency in messaging, formatting, and presentation across client programs • Conduct literature searches as needed • Perform peer QC reviews as needed • Contribute to medical writing operational initiatives such as templates, style guides, and reference management

🎯 Anforderungen

• 5+ years of experience as a medical writer in the CRO/biotech/pharmaceutical field • Bachelor’s degree or higher in a relevant field • Oncology, Infectious Disease, or Vaccine experience desired • Experience writing clinical study reports, protocols, protocol amendments, investigator brochures, Module 2, and Module 5 documents desired • Flexibility to work across multiple therapeutic areas • Experience writing documents according to established processes and document templates • Familiarity with lean authoring approaches and structured content management • Familiarity with requirements for key clinical and regulatory documents, including ICH and US regulatory requirements • Working knowledge of ex-US regulatory requirements desired • Expertise with Microsoft Word and other Microsoft applications • Experience developing documents using document management systems, collaborative authoring tools, and review tools • Comfortable adapting to new tools and technologies • Ability to work independently and collaboratively amid competing priorities • Service-oriented and proactive approach to project management • Excellent conflict management and negotiation skills • Comfortable providing suggestions based on previous experience • Strong written and verbal communication skills in English • Must be based in the UK and legally authorized to work in the UK

🏖️ Vorteile

• Equal employment opportunity regardless of race, color, creed, religion, gender, age, sexual orientation, national origin, disability, veteran status, or any other characteristic protected by law • Permanent, fixed-term, and freelance/contractor employment arrangements are available • Onsite, hybrid, and remote work models are available for London or Manchester

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