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Senior Medical Writer at TransPerfect Andalucía

Career opportunity at TransPerfect located in Andalucía for the position of Senior Medical Writer.

This employment notice was announced on 03 November, 2026 through eurojobs.

com.

Candidates possessing a Bachelor degree are encouraged to submit their application.



Interested individuals should apply directly to TransPerfect for these vacancies in the Medical Writer division.

The estimated application deadline is 18 December, 2026, but please verify the exact date in the official advertisement.

To understand the application process and explore other job openings at TransPerfect, visit the official source or see more details on https://www.

jobseed.

pk.

Private
Bachelor Degree
full-time
Spain

Jobs Date Posted: 03 November, 2026
Jobs Last Date to Apply: 18 December, 2026
Industry: Biotechnology
Jobs Industry Type: Private
Job Hiring Organization: TransPerfect
Experience Required (In months): 60
Occupational Category: Medical Writer
Education Requirements Bachelor Degree
Employment Type: full-time
Advertisement Source: eurojobs.com
Job Location: Andalucía
Country of Appointment: Spain
🎓 Qualifications Required

Further Details

TransPerfect is now recruiting in Andalucía. Apply for the position of Senior Medical Writer. The required qualification is Bachelor. This role is within the Biotechnology 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 TransPerfect

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

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

  • 5+ years of experience as a medical writer in CRO/biotech/pharmaceutical field
  • Bachelor’s degree or higher in a relevant field
  • Experience 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 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
  • 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
  • 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:

  • Review Eligibility: Ensure you meet the core requirements, including at least 5 years of medical writing experience in the CRO, biotech, or pharmaceutical sectors and a Bachelor's degree or higher.
  • Prepare Application Documents: Compile a comprehensive CV/resume detailing your experience, qualifications, and relevant therapeutic area expertise.
  • Visit the Application Portal: Navigate to the official application link provided for this vacancy.
  • Submit Your Application: Complete the online application form accurately and submit your prepared documents through the designated portal.
  • Confirmation: You should receive a confirmation of your application submission.
  • Note on EU Work Permit: This role explicitly states that an EU work permit is required, so ensure you possess the necessary authorization to work in Spain.
  • Deadline: Please ensure your application is submitted on or before the closing date of December 18, 2026.

Application Link:Click here to apply now

Important Note: For any direct inquiries or further information, please refer to the contact details or the eurojobs.com website as provided in the original advertisement.

Additionally, Apply for Medical Writer in Andalucía are available for qualified candidates.


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