Medical Writer

The Senior level Medical Writer will be responsible for the creation of English-language medical writing deliverables ,ensuring the high-quality, timely, and efficient development of clinical and regulatory documents that comply with internal and external standards. This role will 1) be the lead author of regulatory and other scientific documentation, 2)...

The Senior level Medical Writer will be responsible for the creation of English-language medical writing deliverables ,ensuring the high-quality, timely, and efficient development of clinical and regulatory documents that comply with internal and external standards. This role will 1) be the lead author of regulatory and other scientific documentation, 2)...

**Please submit your resume in English** **Scientific Knowledge and Skills**: - Combines a thorough understanding of the therapeutic area with product strategy to ensure communication objectives are met on assigned projects. - Is able to identify and leverage relevant, focused resources to understand the underlying science and product strategy related to...

**Please submit your resume in English** **Scientific Knowledge and Skills**: - Combines a thorough understanding of the therapeutic area with product strategy to ensure communication objectives are met on assigned projects. - Is able to identify and leverage relevant, focused resources to understand the underlying science and product strategy related to...

Prise de poste non définie BAC +3/+4 Paris Nombre de postes non défini CDI À négocier **Description du poste et des missions**: **Poste** Medical Writer **Mission** Le rédacteur médical sera un contributeur actif/auteur principal de la documentation réglementaire et scientifique, gérera la collecte globale de contenu auprès d'équipes...

Created in 2014, Excelya is a people-centered Contract Research Organization (CRO) that excels with care. We offer a personal and authentic experience within a young, ambitious health company on the path to becoming the clinical research leader in Europe thanks to our 800 Excelyates. Our unique one-stop provider service model - leveraging full-service,...

**Responsibilities**: Writing documents relating to the laboratory’s clinical development - Search for information and documents to integrate into clinical study reports - Writing scientific publications (posters, abstracts, articles, protocols, analysis plans, final reports) - Writing and formatting of all clinical study report documents, consistent with...

Hello! Are you ready to Work from Home and transform your career? If you have great consulting skills and know you can consistently delight our customers and help grow our accounts, Modus is the perfect fit for you. Our high performance team helps our clients to build awesome solutions to accomplish their goals and vision. Are you interested in working from...

Job Title: Senior Medical Content SpecialistJob Summary: We are seeking a highly skilled Senior Medical Content Specialist to join our team at IVIDATA Life Sciences. The ideal candidate will have experience in creating high-quality, engaging medical content for regulatory documents and clinical trials.Key Responsibilities:1. Develop and edit clinical and...

**L'offre**: **ROLES ET RESPONSABILITES**: Sous le report de la directrice rédaction médicale et documentation scientifique, vous contribuerez à: - La rédaction de documents cliniques en interface avec les équipes du développement clinique, des affaires règlementaires et de la vigilance (rapports d’études cliniques, brochures investigateurs,...

Responsibilities:Medical writing of all types of regulatory and clinical study documentation including Investigators’ Brochures, clinical study reports, and protocols.Preparation of regulatory responses to health authorities.Preparation of marketing authorisation applications (eCTD module 2).Simultaneously manage several projects and meet tight...

Senior Medical Writer RoleThe Senior Medical Writer will be responsible for creating high-quality, timely, and efficient clinical and regulatory documents that comply with internal and external standards. This role will oversee the development of regulatory and scientific documentation, manage content from cross-functional teams, mentor junior writers, and...

Prise de poste : 01/10/2024 BAC +3/+4 Paris Nombre de poste : 1 CDI De 40k à 50k euros **Description du poste et des missions**: **Position to be filled as soon as possible | Permanent position** - The Paris Brain Institute is a private foundation recognized as being of public interest, dedicated to fundamental and clinical research on the nervous system....

**The Paris Brain Institute (ICM) is recruiting** **_A Medical Monitor (M/F) _** **_Position to be filled as soon as possible. _** **_Permanent position _** **_Paris 13ème - ** - The Paris Brain Institute is a private foundation recognized as being of public interest, dedicated to fundamental _ - and clinical research on the nervous system. On a single...

We are seeking a Regulatory Affairs Expert for Medical Devices to join our team in Paris.Main Responsibilities:Write and coordinate dossiers with contributors (R&D, Production, QA, Clinical, etc.)Ensure dossier constitution aligns with European regulation 2017/745 or specific zone requirements (UK, US, Canada, etc.)Maintain technical files, considering...

**The Paris Brain Institute (ICM) is recruiting** - A Medical Monitor _**(M/F)**_ - **Position to be filled as soon as possible.**_ - **Permanent position**_ - **Paris 13ème**_ - The Paris Brain Institute is a private foundation recognized as being of public interest, dedicated to fundamental and clinical research on the nervous system. On a single site,...

Plan, Write, and Deliver Regulatory DocumentsMeet is seeking a skilled Regulatory Writing Manager to lead the development of high-quality, compliant documents for clinical studies and regulatory submissions. As a key team member, you will be responsible for planning, drafting, and managing the review process for documents related to marketing applications,...

Il s’agit d’une excellente opportunité pour un Concepteur Rédacteur Médical de rejoindre une agence de communication d’environnement médical, spécialisée dans les domaines thérapeutiques innovants (Oncologie, Hématologie, Neurologie, Immunologie, Inflammation, VIH, maladies rares), et de travailler avec les plus grands laboratoires...

Il s’agit d’une excellente opportunité pour un Concepteur Rédacteur Médical de rejoindre une agence de communication d’environnement médical, spécialisée dans les domaines thérapeutiques innovants (Oncologie, Hématologie, Neurologie, Immunologie, Inflammation, VIH, maladies rares), et de travailler avec les plus grands laboratoires...

About the RoleWe are seeking an experienced Product Manager to lead our team in planning and developing innovative products that assist medical writers in generating high-quality Pharmacovigilance documents.This role involves working closely with cross-functional teams to understand the needs of medical writers, designing user-centric tools, and ensuring the...