Medical Writing Officer

About the role

Demo S.A. is looking for a Medical Writing Officer in Athens to write and provide advisory information on curative categories and products. The role covers clinical and non-clinical scientific documentation, regulatory support and expert advice.

Key responsibilities

• Prepare clinical and non-clinical scientific documents for pharmaceutical and medical device products.
• Provide technical and scientific expertise to the 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 Clinical / Non-Clinical Expert on marketing authorization renewals and variations to product information.
• Review clinical trial protocols and clinical study reports.

Required profile

• BSc in Life Sciences, Clinical Pharmacy, Clinical Pharmacology or Medicine; MSc or PhD in a relevant field is an asset.
• At least 3 years of experience in a relevant field, preferably in the pharmaceutical industry or a CRO.
• Fluent in Greek and English.
• Analytical and critical thinking, problem-solving ability, and self-motivation with the ability to meet strict timelines.

Required skills

• Computer literacy.
• Excellent communication skills.

What we offer

• Competitive remuneration.
• Continuous learning and development opportunities.
• A friendly and challenging working environment.