Suneel Kumar

Pharmacovigilance Associate at Apcer Life Sciences

Based in Bengaluru, India

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Seniority

Staff

Department

Healthcare & Human Services

Location

Bengaluru

Industry

Business Consulting and Services

Company size

944

Contact information

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Email

1 credit

s•••••••@apcerls.com

Phone

5 credits

+91 ••• •••• ••••

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Background

About Suneel Kumar

Results-driven Pharmacovigilance Associate with 4 years of dedicated experience in the field, specialising in the monitoring and assessment of adverse event reports. Expertise in ensuring regulatory compliance and enhancing safety data analysis through effective collaboration with cross-functional teams. Proficient in developing and maintaining safety databases, alongside conducting training sessions to elevate pharmacovigilance practices. Committed to contributing to a safer healthcare environment by leveraging knowledge and skills in pharmacovigilance as a Senior Pharmacovigilance Associate.With a Master of Pharmacy degree in Clinical Pharmacy Practice and multiple certifications in pharmacovigilance, signal detection, causality assessment, and statistical reasoning, I am a Pharmacovigilance Associate at APCER Life Sciences, a global leader in drug safety and medical information services.I ensure the safety and quality of drugs and medical devices by performing data entry, review, and quality check of individual case safety reports (ICSR) into the Argus safety database, following the ICH-GCP guidelines, standard operating procedures, and internal policies. I have processed and reviewed hundreds of cases with high accuracy and timeliness, contributing to the compliance and performance of the pharmacovigilance department. I also provide feedback to the team resources and track and maintain quality metrics.I am passionate about improving patient safety and outcomes through pharmacovigilance and clinical pharmacy practice. I have excellent attention to detail, comprehension, and communication skills, and I am fluent in English and Hindi. I am able to work independently and as part of a team, and have a good understanding of the regulatory and pharmacovigilance terminology and obligations. I am always eager to learn new skills and update my knowledge on the latest developments and best practices in the field.

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