Senior Medical Writer

Emploi pas sur LinkedIn

🕒 il y a 1 mois

🇬🇧 Royaume-Uni – Télétravail

⏰ Temps Plein

🟠 Senior

🏥📝 Rédacteur Médical

🗣️🇺🇸🇬🇧 Anglais requis

D'où vient cette offre

Publiée sur la page carrières de TGS, pas via un site d'emploi

Repérée par Remote Rocketship il y a 1 mois

Toujours ouverte sur le site de TGS. Vérifiée il y a 10 heures.

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TGS

501 - 1000 employés

⚡ Énergie

🤖 Intelligence artificielle

Energy • Artificial Intelligence • Digital

TGS est une entreprise leader dans le domaine des données et services énergétiques, issue de la fusion entre PGS et TGS. Elle se spécialise dans la fourniture de données sismiques et de puits de haute qualité aux clients de toute la chaîne de valeur énergétique, permettant des partenariats stratégiques et une prise de décision éclairée. TGS propose également des solutions de stockage et de surveillance du carbone, des opérations d'énergie éolienne et solaire, ainsi que des services d'imagerie avancée et de services numériques grâce à l'analyse et à l'intelligence artificielle. Forte de plusieurs décennies d'expertise en géoscience, TGS s'engage pour l'innovation, la durabilité et le soutien de l'exploration et de la production d'énergie à l'échelle mondiale.

Description

• Lead planning and preparation of high-quality clinical regulatory documents • Produce protocols, publications, study reports, investigator brochures, narratives, and module documents • Lead document execution, 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 instructions • Serve as an expert on the client document management system and related 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 and lead comment resolution meetings • Follow up with team members to resolve outstanding review feedback • Ensure consistency across client programs in messaging, formatting, and document presentation • 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

🎯 Exigences

• 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 • 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 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 • Ability to adapt 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 • Strong written and verbal communication skills in English • Based in the UK and legally authorized to work in the UK

🏖️ Avantages

• 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

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