Senior Medical Writer Role in Spain with TransPerfect

Further Details

This Senior Medical Writer opportunity within TransPerfect's client-facing team in the Canary Islands, Spain, demands exceptional organizational and collaborative skills. The role is pivotal in producing critical clinical and regulatory documentation, supporting drug development under demanding timelines. Additionally, job openings are available for qualified candidates. Successful candidates will possess a Bachelor's degree or higher and a minimum of five years' experience in the pharmaceutical or biotech sectors. The position involves leading document development, coordinating with both internal and external stakeholders, and acting as an expert in client document management systems. Experience in therapeutic areas such as Oncology or Vaccine development, along with a robust understanding of regulatory document requirements (ICH, US, and ex-US), is highly desirable. This role offers a platform for professional growth within a leading organization. TransPerfect champions diversity and inclusion, providing equal employment opportunities. The Senior Medical Writer will play a key part in driving the success of clinical regulatory documents, requiring adaptability and strong analytical skills. Expertise in Microsoft Office Suite and familiarity with collaborative authoring and review tools are essential for this position.

Senior Medical Writer Career Opportunity in Spain

Embark on an exciting career path as a Senior Medical Writer with TransPerfect, a global leader in language and technology solutions. Explore these Medical Writer jobs Canary Islands with competitive benefits. This prominent role is situated in the picturesque Canary Islands, Spain, offering a unique work environment. We are actively seeking a highly skilled and dedicated professional to contribute to our medical writing division, ensuring the highest standards of quality and efficiency in document preparation for drug development.

This position is ideal for an experienced medical writer who thrives in a collaborative setting and possesses a strong understanding of clinical regulatory documentation. You will be instrumental in managing complex projects, coordinating with diverse client teams, and ensuring timely delivery of essential documents. The role emphasizes proactive project management and problem-solving, making it a perfect fit for an individual with excellent interpersonal and communication skills.

• Job Title: Senior Medical Writer
• Location: Canary Islands, Spain
• Company: TransPerfect
• Required Experience: 5+ years in Medical Writing (CRO/Biotech/Pharma)
• Key Responsibilities: Document leadership, project management, stakeholder coordination, adherence to client guidelines.
• Desired Qualifications: Bachelor's degree or higher, therapeutic area experience (Oncology, Infectious Disease, Vaccines), familiarity with regulatory requirements (ICH, US, ex-US).
• Key Skills: Strong written and verbal English communication, adaptability, conflict management, proficiency in MS Office and document management systems.

Skills

• Experience (5+ years) as a medical writer in the CRO/biotech/pharmaceutical field
• Bachelor’s degree or higher in a relevant field
• Oncology, Infectious Disease, or Vaccine experience desired
• Experience desired in writing clinical study reports, protocols, protocol amendments, investigator brochures, module 2, and module 5 documents
• Flexibility to work across multiple therapeutic areas
• Experience writing documents according to established processes and document templates
• Familiarity with lean authoring approaches and structured content management
• Familiarity with the requirements for preparation of key clinical and regulatory documents, including ICH and US regulatory requirements; working knowledge of ex-US regulatory requirements is desired
• Expertise with Microsoft Word and other Microsoft applications
• Experience developing documents using document management systems, collaborative authoring tools, and review tools
• Comfortable adapting to new tools and technologies
• Ability to work both independently and collaboratively in the face of competing priorities
• Service-oriented and proactive approach to project management
• Excellent conflict management and negotiation skills
• Comfortable providing suggestions based on previous experience
• 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 (e.g., quality control [QC], publishing) to ensure timely completion of documents
• Ensure document development adheres to any relevant client processes, templates, and instructional documents
• Serve as an expert on client document management system and related tools, templates, and procedures to ensure efficient document development
• Lead document message development in collaboration with 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 (curate review comments to ensure meetings are efficient)
• Follow-up with individual team members as needed 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 (e.g., templates, style guides, reference management), if needed

How to apply

• 💼 Prepare your Application: Ensure you have a comprehensive curriculum vitae (CV) and any supporting documents that highlight your qualifications and experience.
• 🔎 Review Requirements: Carefully check that you meet all the specified requirements, including the minimum of 5 years of experience as a medical writer in the CRO, biotech, or pharmaceutical sector.
• 🎓 Verify Education: Confirm you possess a Bachelor's degree or a higher qualification in a relevant scientific field.
• 📌 Visit the Application Portal: Navigate to the official Eurojobs website and locate the specific job advertisement for the Senior Medical Writer role.
• 👉 Submit Online: Click on the designated 'Apply Now' or 'Submit Application' button to be redirected to the application form or portal.
• 📝 Complete the Form: Fill out the online application accurately and completely, providing all requested information.
• ⏳ Application Deadline: Please ensure your application is submitted by the closing date of December 18, 2026, to be considered.
• 🌐 Learn More: For additional details about TransPerfect and its family of companies, you can visit their official website.