Senior Medical Writer Vacancy in Spain | Clinical Regulatory Document Specialist

Further Details

Join TransPerfect as a Senior Medical Writer in Castilla-La Mancha, Spain, focusing on clinical regulatory document creation. Successful candidates will benefit from these job vacancies 2026. You will lead document execution, project management, and cross-functional team coordination to ensure the timely completion of vital documents. Your expertise will be key in supporting drug development initiatives, adhering strictly to client guidelines and agency standards for optimal quality and efficiency. This role offers extensive career development within the biotech and pharmaceutical sectors.

Senior Medical Writer Opportunities in Spain

TransPerfect is actively recruiting for a Senior Medical Writer to enhance its specialized medical writing team based in Castilla-La Mancha, Spain. This role is ideal for experienced professionals seeking to make a significant impact in the pharmaceutical and biotech sectors by contributing to crucial drug development documentation. Your expertise will be instrumental in ensuring the timely and accurate delivery of high-quality regulatory documents, supporting global health initiatives.

This position emphasizes cross-functional collaboration, requiring close partnerships with client teams including Clinical Development, Clinical Operations, Biostatistics, Regulatory Affairs, and Program Management. The Senior Medical Writer will be responsible for project management tasks, leading document creation, and ensuring adherence to stringent client and agency guidelines. It's a prime opportunity to advance your career in a leading global organization committed to excellence in life sciences communication.

• Job Title: Senior Medical Writer
• Location: Castilla-La Mancha, Spain
• Company: TransPerfect
• Key Responsibilities: Lead clinical document planning and execution, project management, cross-functional team coordination, and ensure regulatory compliance.
• Required Experience: 5+ years in medical writing within the CRO/biotech/pharmaceutical field.
• Desired Experience: Oncology, Infectious Disease, or Vaccine experience; writing clinical study reports, protocols, investigator brochures, and module 2/5 documents.
• Qualifications: Bachelor’s degree or higher in a relevant field.

Skills

• Minimum five years of medical writing experience within the CRO, biotech, or pharmaceutical industry
• Proficiency in writing clinical study reports, protocols, protocol amendments, investigator brochures, and module documents
• Experience with document management systems, collaborative authoring tools, and review platforms
• Expertise in Microsoft Word and other Microsoft applications
• Strong written and verbal communication skills in English
• Excellent conflict management and negotiation abilities
• Ability to work both independently and collaboratively
• Service-oriented and proactive approach to project management
• Comfort adapting to new tools and technologies

Duties and Responsibilities:

• Lead the planning and execution of clinical regulatory documents
• Manage project timelines, coordinating client contributors and internal resources
• Ensure document development adheres to client processes, templates, and guidelines
• Serve as an expert on client document management systems and procedures
• Lead document message development and data interpretation for shell documents
• Facilitate and lead comment resolution meetings to address review feedback
• Follow up with team members to resolve outstanding review comments
• Ensure consistency in messaging, formatting, and presentation across client programs
• Conduct literature searches as required
• Perform peer QC reviews

How to apply

• 💼 Interested candidates are encouraged to apply for this Senior Medical Writer position in Spain.
• 🔎 Review the detailed job description and responsibilities to ensure your qualifications align with the role's requirements.
• 📝 Prepare a comprehensive CV and any supporting documents that highlight your medical writing experience, particularly in clinical regulatory documents.
• 👉 Visit the official Eurojobs application portal to submit your application.
• 🌐 Access the application link directly through the Eurojobs website.
• 📅 Ensure your application is submitted before the closing date of December 18, 2026.
• ✅ Successful candidates will be contacted by the hiring team for further assessment.