Collect, assess, and process reports of adverse drug reactions (ADRs) from healthcare professionals, patients, and regulatory authorities.
Monitor and evaluate safety data from clinical trials, post-marketing surveillance, and literature to identify trends and potential safety signals.
Ensure compliance with global pharmacovigilance regulations and guidelines (e.g., FDA, EMA, ICH) by accurately documenting and submitting safety reports within required timelines.
Manage Individual Case Safety Reports (ICSRs) by entering data into the pharmacovigilance database, ensuring completeness, accuracy, and adherence to regulatory timelines.
Assist in developing Risk Management Plans (RMPs) and updating them as needed based on emerging safety data.
Conduct periodic signal detection activities, analyzing spontaneous reports, clinical trial data, and literature to identify new safety concerns or risks.
Prepare for and support pharmacovigilance audits and regulatory inspections by maintaining high-quality safety records and ensuring compliance with all legal obligations.
Work closely with regulatory affairs, quality assurance, and clinical teams to support the development and implementation of safety measures for marketed products and those in development.
Educate internal teams and healthcare professionals on the importance of drug safety, reporting procedures, and regulatory requirements.
Qualifications:
Bachelor’s degree in Pharmacy, Medicine, or Life Sciences. A Master’s degree or specialized training in Pharmacovigilance is preferred.
Minimum of 2 years of experience in pharmacovigilance, drug safety, or a related field.
Knowledge of regulatory requirements for pharmacovigilance and post-marketing safety in major markets (e.g., FDA, EMA, WHO).
Experience with safety databases (e.g., Argus, ArisGlobal) and proficiency in ICSR management.
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