Senior Medical Writer at JR Spain Client / Employer: TransPerfect Aragón

Further Details

JR Spain Client / Employer: TransPerfect is now recruiting in Aragón. Apply for the position of Senior Medical Writer. The required qualification is Bachelor. This role is within the Pharmaceuticals industry. A bachelor degree is preferred. The application process commenced on 03 November, 2026 via eurojobs.com. Interested and eligible candidates must submit their applications before the deadline on 18 December, 2026. This is a prime opportunity to join a renowned organization. For a step-by-step application guide and full eligibility criteria, please see the official advertisement on https://www.jobseed.pk.

Senior Medical Writer at JR Spain Client / Employer: TransPerfect

We have an immediate opening for the post of Senior Medical Writer. The job location is Aragón.

Key Requirements:

• Qualification: Bachelor
• Experience: 60 months minimum
• Vacancies: 1

This is a fantastic chance to work with a reputed organization and grow professionally.

Skills

• Lead document execution and project management tasks
• Create, maintain, and communicate project timelines
• Coordinate cross-functional client contributors and stakeholders
• Ensure timely document completion
• Adhere to relevant client processes, templates, and instructional documents
• Serve as an expert on client document management systems and tools
• Lead document message development in collaboration with clients
• Interpret data and create shell documents
• Plan and lead kickoff meetings
• Facilitate resolution of review feedback
• Conduct literature searches as needed
• Perform peer QC review as needed
• Contribute to medical writing operational initiatives
• Experience 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
• 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
• 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

How to Apply for Senior Medical Writer:

• 💼 Prepare Your Application: Ensure your CV is updated and highlights relevant medical writing experience, particularly in clinical regulatory documents.
• 🎓 Review Qualifications: Confirm you meet the minimum requirement of 5+ years of experience as a medical writer in the CRO/biotech/pharmaceutical field and hold a Bachelor’s degree or higher in a relevant discipline.
• 🔎 Gather Supporting Documents: Be ready to provide any necessary certificates or degrees that validate your qualifications.
• 📌 Access Application Portal: Visit the eurojobs.com website and navigate to the specific job listing.
• 👉 Submit Your Application: Click on the 'Apply' button to be directed to the application portal. This position represents excellent JR Spain Client / Employer: TransPerfect jobs Aragón in the region. Follow the on-screen instructions to submit your application.
• ⏳ Application Deadline: Please ensure your application is submitted by 18.12.2026.
• 🌐 Learn More: For more details about TransPerfect, visit their official website.