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Senior Medical Writer at TransPerfect Canary Islands

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

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

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
Job Location: Canary
Address Region: Canary Islands
Country of Appointment: Spain
Employer Department: Medical Writing
Employer Address: canarias, Spain
Street Address: canarias
🎓 Qualifications Required

Further Details

TransPerfect is now recruiting in Canary. 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. 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 Canary Islands.

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

  • 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

How to Apply for Senior Medical Writer:

  • 💼 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.


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