Senior Medical Writer Position in Spain – Clinical Regulatory Writing Opportunities Abroad

Further Details

Seeking a detail-oriented Senior Medical Writer to join a forward-thinking team in Andalusia, Spain, where innovation in clinical documentation drives life-saving treatments. This full-time position requires 5+ years of experience in CRO, biotech, or pharmaceutical environments, with a focus on oncology, infectious diseases, or vaccines. Candidates will lead document development, coordinate with multidisciplinary teams, and ensure adherence to stringent regulatory guidelines. This role represents a prestigious overseas employment opportunity, offering a stable platform for career development within a renowned international organization. Embrace the challenge of shaping clinical narratives that influence global health outcomes while enjoying the benefits of working in Spain's vibrant scientific community.

Senior Medical Writer Opportunities in Spain – Clinical Regulatory Roles

Discover a premier career advancement chance as a Senior Medical Writer with TransPerfect in Spain, where your expertise will directly influence global pharmaceutical developments. This position is tailored for professionals with a minimum of five years of specialized experience in medical writing within CRO, biotech, or pharmaceutical settings, offering a competitive salary and comprehensive benefits package. Ideal candidates will possess a bachelor’s degree or higher in a relevant field, with preferred experience in oncology, infectious diseases, or vaccine-related projects.

• Engage in high-impact clinical regulatory writing, including protocols, study reports, and investigator brochures
• Collaborate with multidisciplinary teams across Clinical Development, Operations, Biostatistics, and Regulatory departments
• Apply lean authoring methodologies and structured content management to optimize document workflows
• Ensure compliance with ICH, US, and ex-US regulatory standards for robust clinical documentation

This overseas job posting represents a significant step in international career development, combining professional challenges with the allure of living and working in Spain. TransPerfect values diversity and inclusivity, providing an environment where your contributions can lead to tangible advancements in medical science.

Skills

• Expertise in clinical regulatory document preparation including protocols, study reports, and investigator brochures
• Strong project management abilities with experience in timeline creation and maintenance
• Proficiency in Microsoft Word and document management systems
• Excellent written and verbal communication skills in English
• Ability to collaborate effectively with cross-functional teams
• Familiarity with ICH and US regulatory requirements
• Experience with lean authoring approaches and structured content management
• Strong conflict management and negotiation skills
• Flexibility to adapt to new tools and technologies
• Prior experience in oncology, infectious disease, or vaccine-related writing

Duties and Responsibilities:

• Lead the execution of clinical regulatory documents while managing project timelines
• Coordinate with client teams and internal resources to ensure timely document completion
• Serve as an expert on client document management systems and templates
• Interpret data to create shell documents for authoring
• Plan and lead kickoff meetings for document development
• Facilitate resolution of review feedback through efficient comment resolution meetings
• Ensure consistency in messaging, formatting, and presentation across client programs
• Conduct literature searches as needed to support document development
• Perform peer quality control reviews to maintain high standards
• Contribute to operational initiatives such as templates and style guides

How to apply

• 💼 Prepare your updated CV highlighting relevant medical writing experience and regulatory knowledge
• 🎓 Ensure your educational documents, including bachelor’s degree or higher, are ready for submission
• 🌐 Visit the official application portal at Apply Now to submit your application online
• 📅 Note the closing date: 18 December 2026 – apply early to secure consideration
• ⚠️ Include a cover letter emphasizing your experience with clinical documents and cross-functional collaboration
• 📩 For inquiries, contact the employer via the provided email or phone number
• 📢 This position is open to candidates requiring no EU work permit, facilitating a smooth application process