Industria Farmaceutica jobs in Spain

Join the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence, as a Senior Medical Writer.

In this role, you will support a Top-5 pharma company, helping deliver best-in-class regulatory and submission documents. You will be fully embedded with our client while being employed by ICON.

1. Independently produce clinical and regulatory documents in collaboration with Principal Medical Writers. These may include Clinical Study Protocols and Clinical Study Reports across Phase 1 to Phase 3 in multiple therapeutic areas.
2. Analyze and interpret data thoroughly to determine the best approach for document composition, applying lean writing strategies.
3. Serve as the primary contact for the study team regarding preparation and timelines of assigned documents, including planning.
4. Facilitate document reviews, ensuring they are submission-ready and approved, working closely with QC personnel and publishing specialists.

• Bachelor’s degree required; Master’s degree preferred.
• 3-5 years of Medical Writing or relevant pharmaceutical experience with scientific and regulatory knowledge.
• Strong writing skills with the ability to convert scientific data into clear, well-structured messages.
• Proficient in independently writing various clinical/regulatory documents, mainly CSRs and Protocols, including leading creation, coordination, review facilitation, and ensuring submission readiness.