What positions are currently available at TransPerfect?

TransPerfect is currently hiring for Senior Medical Writer - Clinical Regulatory Documentation Specialist. These positions offer competitive employment opportunities for qualified candidates.

How can I apply for positions at TransPerfect?

Interested candidates should prepare their complete application including updated CV, educational certificates, experience documents, CNIC copy, and recent photographs. Submit through the specified application method before the deadline mentioned in the job advertisement.

What documents are required when applying to TransPerfect?

Required documents for application to TransPerfect typically include: Updated CV/Resume, CNIC/National Identity Card copy, all educational certificates and transcripts, professional experience certificates, recent passport-sized photographs, domicile certificate, and any other position-specific documents mentioned in the application requirements.

What is the selection process at TransPerfect?

The selection process at TransPerfect typically involves multiple stages: Initial application screening and document verification, written tests or skill assessments for certain positions, personal interviews with the selection committee, final document verification, and official appointment. Only shortlisted candidates will be contacted for subsequent stages.

What is the application deadline for positions at TransPerfect?

The application deadline for current positions at TransPerfect is December 18, 2026. Applications must be submitted before this date to be considered for the selection process.

Where are the job locations for TransPerfect positions?

The job locations for TransPerfect positions are primarily in Comunidad. Specific location details for each position are provided in the detailed job advertisement.

Senior Medical Writer - Clinical Regulatory Documentation Specialist

Join a prestigious team as a Senior Medical Writer in Comunidad Valenciana, Spain, and advance your career in the pharmaceutical and biotech sector.

This role offers an excellent opportunity to work with global clinical regulatory documents, providing a competitive salary and professional growth in a collaborative international environment.

Additionally, vacancies are available for qualified candidates.

Private

full-time

Spain

Jobs Date Posted:	03 November, 2026
Jobs Last Date to Apply:	18 December, 2026
Industry:	Pharmaceuticals and Clinical Research
Jobs Industry Type:	Private
Job Hiring Organization:	TransPerfect
Experience Required (In months):	60
Occupational Category:	Medical Writing
Employment Type:	full-time
Advertisement Source:	Eurojobs
Job Location:	Comunidad
Country of Appointment:	Spain
Employer Department:	Clinical Development
Employer Address:	Comunidad Valenciana, Spain
Work Hours:	Standard business hours

🎓 Qualifications Required

📌 Job Positions:

Senior Medical Writer

Further Details

TransPerfect is hiring a Senior Medical Writer to manage clinical regulatory documentation in Spain. This position involves cross-functional collaboration on protocols, clinical study reports, and investigator brochures for drug development projects, offering significant career development for experienced professionals.

Career Opportunities for Senior Medical Writer

TransPerfect is currently seeking a highly motivated Senior Medical Writer to join their expert team in Spain. This role is perfect for professionals looking to utilize their pharmaceutical experience to impact global clinical regulatory document standards. You will enjoy a professional work environment focused on career development and innovation.

Position: Senior Medical Writer
Location: Comunidad Valenciana, Spain
Sector: Private (Pharmaceutical/Biotech)
Key Focus: Clinical Regulatory Documentation

Sr.#	Job Title	Required Qualifications	Location	Experience	Vacancies
1	Senior Medical Writer	Bachelor	Comunidad Valenciana	5+ Years	1

Skills

Expertise in Microsoft Word and document management systems
Strong written and verbal communication skills in English
Proven ability to interpret complex data and create shell documents
Advanced knowledge of ICH and regulatory requirements
Excellent conflict management and negotiation abilities
Experience with lean authoring and structured content management

Duties and Responsibilities:

Lead the planning, preparation, and execution of high-quality clinical regulatory documents
Coordinate with cross-functional stakeholders including Biostatistics and Regulatory teams
Manage project timelines and facilitate effective review meetings for document feedback
Ensure all documentation aligns with client templates, processes, and international guidelines
Perform peer quality control reviews and conduct necessary literature searches
Collaborate on operational initiatives such as updating style guides and reference management

How to apply

👉 Visit the official application page at the link provided below.
📝 Ensure your CV is updated, highlighting your experience in CRO, biotech, or pharmaceutical writing.
💼 Prepare a professional cover letter addressing your expertise in oncology or infectious diseases.
⏳ Submit your application before the closing date of 18 December, 2026.
🌐 Follow all instructions on the TransPerfect portal to complete your submission.