Senior Medical Writer - Freelancer FR speaking

New

ExcelyaPharmaceutical/health industry

France. Greece. Belgium. Luxembourg. Netherlands. everywhere in EU.Part-TimeSenior

Salary not disclosed

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Job Details

Languages: English, French

Requirements

Degree in Life Sciences
Previous working experience in the pharmaceutical/health industry
Experience in writing: ICF (FR/ENG)
Experience in writing: non-opposition letters (FR/ENG)
Experience in writing: lay summaries
Experience in writing: posters/manuscripts
Experience in writing: protocols (Phase I-III)
Experience in writing: CSR
Experience in writing: CTDs (2.4-2.7)
Experience in medical device-related documents (CEP/CER/PMCF/PSP) considered a plus
Able to work autonomously
Experience in clinical documents for interventional and non-interventional studies
Critically evaluate scientific data
Project management skills
Able to review TFLs and participate in data review meetings
Fluent in English and French language

Responsibilities

Develop, write, and edit a wide range of scientific and medical documents, ensuring accuracy, clarity, and compliance with regulatory and journal requirements
Produce materials such as manuscripts, abstracts, posters, slide decks, and other scientific communications
Prepare and review patient-facing documents, including Informed Consent Forms (FR/ENG), non-opposition letters (FR/ENG), and Lay summaries
Write and contribute to clinical and regulatory documents, including Clinical study protocols (Phase I–III), Clinical Study Reports (CSRs), and Common Technical Document sections (CTD 2.4–2.7)
Support medical affairs activities such as review of promotional and non-promotional materials, medical training for internal and external stakeholders, and medical information services
Collaborate with cross-functional teams, subject matter experts, and clients to ensure scientific accuracy and alignment with project objectives

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