The role provides medical expertise to evaluate safety data from various sources within the pharmacovigilance process
Job Summary
The role provides medical expertise to evaluate safety data from various sources within the pharmacovigilance process.
This position serves as a senior technical leader responsible for preparing aggregate reports and managing surveillance activities for selected products.
Candidates must possess a medical degree and three years of clinical practice experience to ensure regulatory compliance and quality service delivery.
Matching Summary
The role provides medical expertise to evaluate safety data from various sources within the pharmacovigilance process.
Skills & Requirements
Must-have
Medical degree from accredited school
Three years clinical medicine experience
Knowledge of GCP and ICH guidelines
Experience with ICSR and aggregate reports
Ability to review adverse event narratives
Nice-to-have
Two years pharma experience preferred
Valid medical license in work region
Strong verbal and written communication skills
Experience with matrix management activities
Proficiency in multiple safety databases
Key Requirements
Medical degree from accredited international school
Three years post-graduate clinical practice experience
Sound knowledge of global clinical research regulations
In-depth knowledge of departmental SOPs
Adequate computer skills including Microsoft Office