Senior Medical Writer – Eye Health & Inflammation

IQVIA; Brussel Hoofdstad; On-site; EUR 60,000 - 90,000; Full time

Job summary

IQVIA is seeking a full-time Medical Writer in Belgium to develop clinical documents including CT Reports, CT Protocols, IBs, and submission materials. The role emphasizes writing for eye health and inflammation, with senior-level experience preferred.

You will embed in sponsor processes, manage timelines, and collaborate with cross-functional teams to ensure high-quality deliverables. Responsibilities include document management in EDMS, drafting and editing, attending meetings, and finalizing

Qualifications

• Bachelor’s degree in a scientific, clinical, regulatory, or related field required; advanced degree preferred.
• Approximately 5 years of medical writing experience in biopharma, biotech, or CRO.
• Strong knowledge of global regulatory requirements (ICH, FDA, EMA).
• Experience leading writing for complex documents and cross-functional teams.
• Excellent written and verbal communication; detail-oriented and deadline-driven.
• Proficient in Word and document formatting; familiar with eDMS and templates.

Responsibilities

• Deliver medical writing services for CTRs, CT protocols, amendments, IBs, and submission documents.
• Manage project timelines, meetings, and writing workflows with sponsor systems.
• Lead drafting and revision cycles, ensuring alignment with peer reviews.
• Perform QC checks and finalize documents for submission and archiving.
• Collaborate with cross-functional teams across clinical development.

Skills

Medical writing

Lead writing activities

EDMS experience

Microsoft Word

Document formatting

Education

Bachelor’s degree in science/clinical/regulatory

Advanced degree preferred

Tools

EDMS

Microsoft Word

Job description

IQVIA is seeking a full-time Medical Writer in Belgium to develop clinical documents including CT Reports, CT Protocols, IBs, and submission materials. The role emphasizes writing for eye health and inflammation, with senior-level experience preferred.

You will embed in sponsor processes, manage timelines, and collaborate with cross-functional teams to ensure high-quality deliverables. Responsibilities include document management in EDMS, drafting and editing, attending meetings, and finalizing