Senior Medical Writer Position in Spain - Competitive Salary & Career Growth

Further Details

A Senior Medical Writer is required at TransPerfect in Castilla León, Spain, to contribute to clinical and regulatory document development. Successful candidates will benefit from these career opportunities. The successful candidate will lead the creation of protocols, study reports, and investigator brochures, ensuring alignment with client guidelines and regulatory requirements. With a minimum of 5 years of experience in the pharmaceutical or biotech industry, the role demands expertise in ICH and US regulatory frameworks, as well as familiarity with lean authoring and structured content management. This position offers a competitive salary and the chance to work on international projects, providing a platform for professional growth in the medical writing domain.

Senior Medical Writer Opportunities in Spain

TransPerfect is offering a dynamic career opportunity for a Senior Medical Writer in Castilla León, Spain. This role is integral to the development of high-quality clinical and regulatory documents, supporting drug development initiatives on a global scale. Candidates with a strong background in medical writing and a passion for precision will find this position aligning with their career goals.

• Key Requirements: 5+ years of experience in medical writing within the pharmaceutical industry
• Essential Skills: Expertise in ICH and US regulatory requirements, proficiency in Microsoft Office, and experience with document management systems
• Preferred Qualifications: Experience in oncology, infectious diseases, or vaccines
• Location: Based in Castilla León, Spain, with opportunities for remote collaboration
• Benefits: Competitive salary, professional growth, and involvement in international projects

This position is ideal for professionals seeking to make a significant impact in the healthcare writing sector. Apply now to join a leading team at TransPerfect and contribute to groundbreaking medical advancements.

Skills

• 5+ years of experience as a medical writer in CRO, biotech, or pharmaceutical field
• Bachelor’s degree or higher in a relevant field
• Experience in oncology, infectious disease, or vaccine writing
• Proficiency in writing clinical study reports, protocols, protocol amendments, investigator brochures, module 2, and module 5 documents
• Flexibility to work across multiple therapeutic areas
• Familiarity with lean authoring approaches and structured content management
• Knowledge of ICH and US regulatory requirements; working knowledge of ex-US regulatory requirements is desired
• Expertise with Microsoft Word and other Microsoft applications
• Experience with document management systems, collaborative authoring tools, and review tools
• Ability to adapt to new tools and technologies
• Strong project management skills with a service-oriented and proactive approach
• Excellent conflict management and negotiation skills
• Strong written and verbal communication skills in English

Duties and Responsibilities:

• Lead the execution of documents, including project management tasks such as creating, maintaining, and communicating timelines
• Coordinate cross-functional client contributors and stakeholders as well as internal resources to ensure timely completion of documents
• Ensure document development adheres to relevant client processes, templates, and instructional documents
• Serve as an expert on client document management systems and related tools, templates, and procedures
• Lead document message development in collaboration with the client
• Interpret data and create shell documents to support authoring
• Plan and lead kickoff meetings
• Facilitate resolution of review feedback, including planning and leading comment resolution meetings
• Follow-up with individual team members to resolve outstanding review feedback
• Ensure consistency among client programs in terms of messaging, formatting, and presentation of documents
• Conduct literature searches as needed
• Perform peer QC review as needed
• Contribute to medical writing operational initiatives, such as templates, style guides, and reference management

How to apply

To apply for the Senior Medical Writer position, please follow these steps:

• 💼 Prepare your updated CV, highlighting relevant medical writing experience and regulatory knowledge.
• 📋 Include a cover letter detailing your interest in the role and how your skills match the requirements.
• 📅 Submit your application by 18 December, 2026, via the official application link.
• 🌐 Visit the application portal: Apply Now
• 📞 For inquiries, contact the employer through the provided channels.
• ⚠️ Ensure all documents are in English and formatted professionally.

TransPerfect is an equal opportunity employer, welcoming applicants from all backgrounds to apply.