Bindiya Patel Email & Phone Number | 5 years of experience in pharmacovigilance in both clinical trial and post marketed products. •Experienced in case processing, triage and, narrative writing of Individual Safety Case Reports (ICSRs) for Adverse Events (AEs) and Serious Adverse Events reports from Spontaneous, solicited, and clinical trial sources. •Thorough knowledge of drug information process, medical terminology, and diagnostic tests. •Expertise in monitoring and tracking Serious Adverse Events, serious and non-serious adverse drug reactions, and other medically related project information. •Contributed to the preparation, writing and review of the periodic aggregate reports. •Researcher and provider of medical and scientific information to health care professionals and to various functional areas within the organization. •Data analysis, medical and scientific literature searches using critical judgment and professional/ scientific expertise to support projects or queries. •Experience in working in database software Argus, Microsoft access. •Experience in quality checks and compliance. •Strong communication and organization skills. •Exceptional ability to manage multiple projects and prioritize work.

Bindiya Patel

5 years of experience in pharmacovigilance in both clinical trial and post marketed products. •Expe...
Charlotte, North Carolina, United States

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Bindiya Patel’s Location Charlotte, North Carolina, United States

Bindiya Patel’s Current Industry Perrigo

Bindiya Patel’s Prior Industry Actelion | Mallinckrodt Pharmaceuticals

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Pharmacovigilance Specialist I

2022-07-01 00:00:00 - Present

Drug Safety Specialist

2019-08-01 00:00:00 - 2022-06-01 00:00:00

Pharmacovigilance specialist

2018-07-01 00:00:00 - 2019-07-01 00:00:00

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Bindiya Patel is a 5 years of experience in pharmacovigilance in both clinical trial and post marketed products. •Experienced in case processing, triage and, narrative writing of Individual Safety Case Reports (ICSRs) for Adverse Events (AEs) and Serious Adverse Events reports from Spontaneous, solicited, and clinical trial sources. •Thorough knowledge of drug information process, medical terminology, and diagnostic tests. •Expertise in monitoring and tracking Serious Adverse Events, serious and non-serious adverse drug reactions, and other medically related project information. •Contributed to the preparation, writing and review of the periodic aggregate reports. •Researcher and provider of medical and scientific information to health care professionals and to various functional areas within the organization. •Data analysis, medical and scientific literature searches using critical judgment and professional/ scientific expertise to support projects or queries. •Experience in working in database software Argus, Microsoft access. •Experience in quality checks and compliance. •Strong communication and organization skills. •Exceptional ability to manage multiple projects and prioritize work.