Sucharita Ramisetty
IIM-Calcutta-APSPM || Digital Transformation Program Manager || CSM®
- Role
- Associate Director - Program Management at Capgemini Invent
- Location
- Hyderabad, TG, IN
- LinkedIn followers
- 500 followers
About Sucharita Ramisetty
15 years of experience in Pharmacovigilance Client Governance, Argus Safety, Medical Device Vigilance, Vaccine reporting & Empirica Signal. Worked as Business Analyst for multi-tenant/on-premise projects for IT GxP systems and implementation • Abreast with E2B R3, eVAERS, Argus 8.4, MFDS R3 & Device - Combination Products Regulations• SPOC for Empirica Signal & ARGUS, IQVIA Vigilance Platform (IVP) implementation projects for top Pharma MNCs.• Validation Support, PQ Execution support and authoring WI• Hands on work experience in Case Processing, Quality Review and medical evaluation for 3 years• Well versed with Argus, Argus Japan Configuration and Validation for 12 years• Successful in transitioning and Process Trainer• Experience in writing Software specifications, Use cases, and Test scenarios for medium to large-scale projects.• Training on Argus and Pharmacovigilance process• Expert in providing Hypercare and Handles support tickets using SNOW ticketing Tool• Planning Conference Room Pilot sessions, System upgrades and Account Management
Experience
Associate Director - Program Management
Aug 2025 — Present · Hyderabad, IN
Digital R&D Patient Safety & PharmacovigilanceDigital Transformation in Drug Safety Systems Digital Product Strategy NextGen PV Apps Program Management
Education
Acharya Nagarjuna University
Master of Pharmacy, Pharmaceutics and Drug Design
2007 — 2009
Indian Institute of Management, Calcutta
Advanced Programme in Strategic Project Management - Batch 5
2024 — 2025
Skills
- Pharmaceutics
- Custom Reports
- Clinical Trials
- Cbd Tool
- Obiee
- Argus Safety
- CRO
- Gcp
- Argus Console
- Validation
- Clinical Data Management
- Analytics
- Quality Assurance
- Computer System Validation
- Ich-Gcp
- Regulatory Submissions
- Cognos
- Pharmacovigilance
- Regulatory Affairs
- Medical Writing
- Configuration Management
- Meddra
- Traceability Matrix
- Risk Assessment
- Pharmaceutical Industry
- Drug Safety
- Hp Quality Center
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