Drug safety physician

Overall oversight of company’s products safety profile including signal management processes and risk management processes

Preparation of quality control documents, i.e. Standard Operation Procedures and operational guidelines.

Providing overall and medical assessment of adverse drug reaction reports (clinical implications of safety data from non-interventional studies, literature and other information sources) and adverse event reports (clinical implications of safety data from pre-clinical and clinical studies).

Preparation of pharmacovigilance-related regulatory documentation (aggregate reports

PSURs, RMPs) for innovative, original and key products, communicate safety profile.

Preparation of safety overviews of various medicinal products to the company and relevant authorities.

Fantastic opportunity to join Pharmaceutical company with opportunity to develop further with the organisation.

Chemical industry, manufacture of pharmaceutical products

Our client is a leading pharmaceutical company with its own scientific research base for development of human drug products