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Senior Medical Writer at TransPerfect Galicia

Career opportunity at TransPerfect located in Galicia 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 Writing 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: Pharmaceuticals
Jobs Industry Type: Private
Job Hiring Organization: TransPerfect
Experience Required (In months): 60
Occupational Category: Medical Writing
Education Requirements Bachelor Degree
Employment Type: full-time
Advertisement Source: eurojobs.com
Job Location: Galicia
Country of Appointment: Spain
Employer Department: Medical Writing
Work Hours: Full-time
🎓 Qualifications Required

Further Details

TransPerfect is now recruiting in Galicia. 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 TransPerfect

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

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 internal resources
  • Ensure document development adheres to client processes and templates
  • Serve as an expert on client document management system and related tools
  • Lead document message development in collaboration with clients
  • Interpret data and create shell documents for authoring
  • Plan and lead kickoff meetings
  • Facilitate resolution of review feedback
  • Plan and lead comment resolution meetings
  • Follow up with team members to resolve outstanding review feedback
  • Ensure consistency among client programs
  • 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
  • Familiarity with lean authoring approaches and structured content management
  • Familiarity with requirements for key clinical and regulatory documents
  • Expertise with Microsoft Word and other Microsoft applications
  • Experience developing documents using document management systems and collaborative tools
  • Comfortable adapting to new tools and technologies
  • Ability to work 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 planning and preparation of high-quality clinical regulatory documents
  • Partner cross-functionally with client teams in Clinical Development, Clinical Operations, Biostatistics, Regulatory, and Program Management
  • Produce protocols, publications, study reports, investigator brochures, narratives, and module documents
  • Support drug development under brisk timelines
  • Interpret data and create shell documents to support authoring
  • Facilitate resolution of review feedback including planning and leading comment resolution meetings
  • Ensure consistency among client programs in terms of messaging, formatting, and presentation of documents
  • Perform peer QC review as needed
  • Contribute to medical writing operational initiatives (e.g., templates, style guides, reference management)
  • Adhere to client and agency guidelines for document creation
  • Manage competing priorities effectively

How to apply

How to Apply for Senior Medical Writer:

  • Visit the application portal: Navigate to the official TransPerfect careers page via the provided link.
  • Locate the job posting: Find the 'Senior Medical Writer | Spain' advertisement for Galicia.
  • Review the full description: Carefully read through the job description and requirements to ensure alignment with your qualifications.
  • Prepare your application documents: Ensure your CV is updated and highlights relevant experience in medical writing, clinical documentation, and any therapeutic area specializations (Oncology, Infectious Disease, Vaccine).
  • Submit your application: Click on the 'Apply' button and follow the on-screen instructions to submit your application online.
  • Required Information: You may be asked to provide personal details, educational qualifications, employment history, and other relevant professional information.
  • Application Deadline: Please ensure your application is submitted by the closing date of December 18, 2026. Late submissions will not be considered.
  • Confirmation: Look for a confirmation email upon successful submission of your application.


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