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About the Role
EARON International leader in life sciences recruitment is looking for a Medical Writer for its client, an international CRO based in Paris. Scope : - Scientific writing support for pre-clinical and clinical study documents. - You will have considerable direct contact with clients, especially with the clinical teams and will work together at the company with Clinical Data Managers, and Statisticians to produce high quality documents.
Key Responsibilities : - Write investigational medicinal product dossiers, investigator brochures, clinical study concept protocols, protocols and protocol amendments, informed consent forms, assent forms, clinical study reports, and summary (Module 2) documents for licensing applications - Compile and publish complex documents (e.g., clinical study reports) - Write patient narratives and other pharmacovigilance documents (e.
g., DSURs, PBRERs, RMPs) - Write and edit publications for peer-reviewed scientific/medical journals - Write abstract...
Key Responsibilities : - Write investigational medicinal product dossiers, investigator brochures, clinical study concept protocols, protocols and protocol amendments, informed consent forms, assent forms, clinical study reports, and summary (Module 2) documents for licensing applications - Compile and publish complex documents (e.g., clinical study reports) - Write patient narratives and other pharmacovigilance documents (e.
g., DSURs, PBRERs, RMPs) - Write and edit publications for peer-reviewed scientific/medical journals - Write abstract...
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