DEMO S.A. Pharmaceutical Industry
medical writing officer
Oct 8, 2026 · DEMO S.A. Pharmaceutical Industry
Αττική·Oct 8, 2026
ΑττικήOn SiteΕπαγγέλματα ΥγείαςPermanentFull Time
JOBILY AI SUMMARY
What you'll do
- Prepare clinical and non-clinical scientific documents for pharmaceutical and medical device products
- Provide technical and scientific expertise to Regulatory Affairs and Business Development departments
- Prepare Risk Management Plans (RMPs) and Risk Minimization Materials (RMMs)
- Maintain and archive records related to departmental activities
- Prepare and update Standard Operating Procedures (SOPs) in the absence of the Senior Medical Writing Officer
- Communicate with partner companies in Greece and abroad on medical and scientific matters
- Act as a Clinical / Non-Clinical Expert for marketing authorization renewals and variations to product information
- Review clinical trial protocols and clinical study reports
Key requirements
- 3+ years' experience
- Medical writing and clinical and non-clinical scientific documentation
- Regulatory affairs support, including marketing authorization renewals and variations
- Risk Management Plans (RMPs) and Risk Minimization Materials (RMMs)
- Standard Operating Procedures (SOPs), clinical trial protocols and clinical study reports
- Computer literacy
- Greek and English language fluency
- Life Sciences / Clinical Pharmacy / Clinical Pharmacology / Medicine / Any Field
Benefits
- Competitive remuneration, continuous learning and development opportunities, and a friendly and challenging working environment.
About the job
In this dynamic and fast growing environment we are looking for a high caliber Medical Writing Officer who will be responsible for writing and providing advisory information on curative categories and products. Medical Writing Officer Main duties and responsibilities: - Prepares clinical and…
