Medical Writer: Oncology & Clinical Docs Expert (Belgium)

Alsinova; Belgique; Remote; EUR 42,000 - 64,000; Full time

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Job summary

Alsinova, a CRO within the Astek Group, is seeking a Medical Writer in Belgium. You will synthesize literature, draft and edit clinical development documents, and ensure regulatory compliance.

Collaboration with clients and cross‑functional teams is key as you contribute to high-quality scientific content in French and English. The role requires a scientific degree and at least one year of Medical Writing experience, with strong MS Word/Excel/PowerPoint and EndNote proficiency.

Qualifications

• Science degree and ability to understand scientific information.
• Minimum 1 year of Medical Writing experience.
• Clear written communication in French and English.
• Proficient in Word, Excel, PowerPoint and EndNote.
• Familiarity with clinical research and regulatory guidelines.

Responsibilities

• Synthesize literature findings into reports for various therapeutic areas.
• Write, edit and update clinical development documents with high accuracy.
• Lead QC reviews of clinical documents and support multiple drafts.
• Ensure quality of documents per ICH-GCP and regulatory standards.
• Collaborate with authors/clients on scientific content.
• Prepare manuscripts, posters, abstracts as needed.

Skills

Scientific writing

1 year experience

French & English

MS Office proficiency

EndNote

Clinical research familiarity

Education

Scientific degree

Tools

Word

Excel

PowerPoint

EndNote

Job description

Alsinova, a CRO within the Astek Group, is seeking a Medical Writer in Belgium. You will synthesize literature, draft and edit clinical development documents, and ensure regulatory compliance.

Collaboration with clients and cross‑functional teams is key as you contribute to high-quality scientific content in French and English. The role requires a scientific degree and at least one year of Medical Writing experience, with strong MS Word/Excel/PowerPoint and EndNote proficiency.