Akhila Viswanathan
@akhilaviswanathan
I process and review pharmacovigilance cases, improving safety data quality and compliance.
United Arab EmiratesWhat I'm looking for
At Qinecsa Solutions, I process and review safety cases involving intra-uterine devices, pregnancy, literature, post-marketing sources, and ESM Gateway intake. I manage E2B R2/R3 regulatory distribution, site follow-up, discrepancy reconciliation, and case-quality checks.
Previously at Cognizant, I processed pharmacovigilance cases across 15+ drugs and progressed to Quality Reviewer. Across 7+ years in drug safety, I’ve supported audits, trained new joiners, facilitated team huddles, and worked with ARISg, MedDRA, WHO-DD, ATC coding, Medidata Rave EDC, and Medidata Coder.
Experience
Work history, roles, and key accomplishments
Senior Drug Safety Associate
Qinecsa Solutions
Jun 2021 - Present (5 years 3 months)
Processed and reviewed safety cases involving intra-uterine devices, pregnancy, literature, post-marketing sources, and ESM gateway cases. Managed E2B R2/R3 distribution, coordinated follow-up, and supported quality and audit activities.
Education
Degrees, certifications, and relevant coursework
Institute of Clinical Research India
Post Graduate Diploma, Clinical Research and Pharmacovigilance
2018 - 2019
Post Graduate Diploma in Clinical Research and Pharmacovigilance from the Institute of Clinical Research India, Mumbai.
Availability
Location
United Arab EmiratesAuthorized to work in
Job categories
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