Job Description
Job Description
To complete IDL (Iran Drug List) form for new molecules (translation, review, and selection of all scientific information related).
Coordination with market access team for IDL form completion.
Entry of pharmacovigilance data into the ADR (Adverse Drug Reactions) website of the IFDA.
Review, follow-up, and registration of data related to adverse drug reactions (ADRs).
Review and monitoring of medical literature and articles from a pharmacovigilance perspective.
Review of scientific brochures and comparing with reference brochures.
In the absence of the Medical Compliance & PV Manager, this person is responsible for establishing a control system to ensure the availability of adverse event phone lines and documenting these controls.
Requirements:
Fluency in English
Excellent written and verbal communication skills for reporting and training purposes.
Strong analytical and problem-solving skills to assess compliance risks and develop effective solutions.
Strong skills in Microsoft Office.
2 to 3 years of experience in pharmaceutical industry.
Degree in Medical Science, Life Science or a related field is a plus.
