Senior Medical Writer Remote

buscojobs España; La Coruña; A distancia; EUR 40.000 - 60.000; Jornada completa

Descripción de la vacante

A leading global Contract Research Organization is seeking a Medical Writer / Technical Reviewer to ensure the scientific accuracy and quality of medical content. The role involves collaboration across international teams and requires a strong background in the Pharma/Biotech industry, with excellent writing skills and fluency in English and additional languages.

Formación

• 3-5 years experience as a Medical Writer or Reviewer in Pharma/Biotech.
• Excellent medical writing skills.
• Ability to work independently and in teams.

Responsabilidades

• Ensure scientific accuracy and referencing quality of medical assets.
• Review content for compliance with regulatory guidelines.
• Track asset quality data for reporting.

Conocimientos

Medical writing

Content review

Collaboration

Fluency in English

Fluency in German

Fluency in French

Educación

PharmD, MD, PhD, or Master's degree

Herramientas

Veeva Vault

Descripción del empleo

TFS HealthScience is a leading global, mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service capabilities, resourcing, and functional service provider (FSP) solutions.

Position: Medical Writer / Technical Reviewer

The Medical Writer / Technical Reviewer will be responsible for ensuring the scientific accuracy, data and referencing quality, appropriate style, and correct branding of scientific/medical assets for the sponsor globally. The role involves working in an international and cross-functional environment, following global and local guidelines, and collaborating closely with internal and external stakeholders to ensure the highest quality of sponsor assets and gather data on asset quality and agency performance.

1. Perform data/referencing quality checks of scientific/medical assets, ensuring all content is scientifically accurate and appropriately supported by reference documents.
2. Review content and identify any non-compliances with local regulatory guidelines.
3. Perform actions in the Review and Approval platform (Veeva Vault), such as reference tagging or claims object creation.
4. Track asset quality data for internal and external reporting.

Qualifications

• Experienced Medical Writer or Medical Content Reviewer (3-5 years) with a scientific background and degree (PharmD, MD, PhD, or Master's), with at least 3 years producing or reviewing content for the Pharma/Biotech industry.
• Excellent medical writing skills.
• Fluent in oral and written English and one or more of these languages: German, French.
• Ability to work within a team or across multiple teams (including remotely) as well as independently.
• Prior experience working in content creation for Biotech/Pharma is advantageous.
• Prior experience with the Pharmaceutical Content Review process and/or Veeva Vault is advantageous.

About TFS HealthScience

As a full-service, global Contract Research Organization (CRO), we build solution-driven teams working towards a healthier future. Bringing together over 800 professionals, TFS delivers tailored clinical research services in more than 40 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.

Our core values of Trust, Quality, Passion, Flexibility, and Sustainability guide our decision-making at all levels of the organization. By aligning on these fundamental values, we cultivate a unified force, geared towards innovation and excellence.