Swaranjali Bhusa
Clinical Data Processor | QA | Clinical Research & Pharmacovigilance | SAS | LIMS | Regulatory Documentation | ICH-GCP/GMP
- Role
- Clinical Data Processor at Clario
- Location
- Bengaluru, KA, IN
- LinkedIn followers
- 500 followers
About Swaranjali Bhusa
I am a life sciences professional with experience in QA documentation, regulatory submissions, and GMP-based clinical manufacturing. I have worked on CTD dossier preparation, SOP and CAPA management, audit readiness, PAS-X based batch execution, LIMS sample workflows, and coordination with QA/QC during clinical batch operations.I am also familiar with pharmacovigilance concepts, ICSR fundamentals, MedDRA, and ICH guidelines including E2A and E2B. Through hands-on work with clinical trial data, SAS programming, discrepancy checks, and essential documents like CRFs and ICFs, I have built a solid understanding of clinical research workflows.I am strongly interested in building my career in clinical research and pharmacovigilance, where I can combine my QA, data review, and regulatory skills to contribute to high-quality and compliant clinical operations.
Experience
Clinical Data Processor
Feb 2026 — Present · Bengaluru, IN
Education
H.P.T. ARTS and R.Y.K. SCIENCE COLLEGE
BSc Biotechnology
REVA University
MSc Biotechnology, Biotechnology
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