Open to opportunities

Anusha Nandeesh

@anushanandeesh

Message

I process pharmacovigilance safety cases, triage adverse events, and deliver accurate regulatory-compliant ICSR data.

India

Message

What I'm looking for

I'm looking for a pharmacovigilance role where I can contribute to accurate, timely safety case processing, literature review, regulatory compliance, and continuous safety-data quality improvement.

At Norwich Clinical Services, I triage and process individual case safety reports, including intake, duplicate checks, registration, data entry, and assessment of adverse-event validity, seriousness, and expedited reporting requirements.

I also review literature for case safety reports, conduct global safety database duplicate searches and SDEA checks, and code medical information using MedDRA and WHO Drug dictionaries. I maintain accurate, timely safety data while following ICH-GCP, GVP, client SOPs, and global pharmacovigilance guidelines.

Experience

Work history, roles, and key accomplishments

Current

Safety Associate

Current

Norwich Clinical Services

Jan 2024 - Present (2 years 7 months)

Responsible for case intake, duplicate check, registration, and data entry of individual case safety reports into the safety database. Review and evaluate adverse event case information to determine validity, seriousness, and expedited status as per client and internal policies.

ICSR Case Processing Literature Screening MedDRA Coding Canadavigilance MS Word Excel PowerPoint