Enthusiastic, dedicated Pharmacovigilance expert with three years of experience in Clinical and Pharmacovigilance, including Case processing which includes booking, data entry, MedDRA Coding, Narrative Writing.
Medical Evaluation of ICSR, Aggregate Reports, Signal Detection, Risk Management, Benefit-Risk.
Analysis, Risk Evaluation, Mitigation Strategies, and medical assessment/ evaluation as well.
Eager to contribute to team success through hard work, attention to detail, and excellent organizational skills,
Trained & Certified with a Clear understanding of Pharmacovigilance and Clinical trials.
Motivated to learn, grow and excel in the field.
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