Tejaswi Poda

Experienced clinical research and pharmacovigilance professional seeking to contribute to patient safety and regulatory compliance through accurate drug safety reporting and trial support.

Drug Safety Associate - Accenture Solutions Pvt. Ltd. - Bangalore

(2022-02)

• Monitoring, evaluating, and reporting adverse drug reactions (ADRs) to ensure patient safety.
• Handling end-to-end (intake, fde) of processing individual case safety reports (ICSRs) within clinical trial protocols (such as those managed by Hcelgene, Rave and Interim using Medidata Rave) must comply strictly with ICH-GCP guidelines and applicable regulatory requirements.
• Ensuring timely submission of safety data to global health authorities.
• Reviewing and updating safety information in clinical trial documentation.
• collaborating with cross-functional teams to streamline pharmacovigilance activities
• Daily review of workflows and complex randomized controlled trials (RCTs) during team huddles to ensure process efficiency, timely resolution of issues and RCT prioritization to achieve daily targets by maintaining quality and productivity.

Clinical Research Associate - Ascentrik Research Pvt. Ltd. - Pune

(2019-11 - 2020-11)

• Performed MedDRA coding, event assessment, and narrative writing for adverse event reporting.
• Involved in clinical trials, drug research, data extraction, and secondary research.
• Screened pre- and post –conference materials and analyzed company landscapes.

Master of Pharmacy - Pharmaceutical Analysis - QIS College of Pharmacy (2021)

Bachelor of Pharmacy - Chalapathi Institute of Pharmaceutical Sciences (2018)