Industrial Trainee
- Undergone industrial training in quality control and R&D department
To leverage my knowledge, skills, and dedication to contribute effectively in e dynamic professional environment, while continuously growing and delivering quality results that support organizational goals and drive meaningful impact
Clinical Data Management: Knowledge of EDC systems (Rave, Veeva), CTMS, Annotated CRFs, DMP, UAT
Knowledge of SOPs & Regulatory Compliance– Understanding of SOPs, Work Instructions, GCP, and clinical trial regulations
Clinical Trial Process: understanding of clinical trial phases, protocol adherence, informed consent, and regulatory guidelines
Documentation & Record Management – Skilled in accurate preparation, maintenance, and storage of project/technical documents with version control and audit compliance
Quality Control & Attention to Detail– Able to review work for accuracy, completeness, and compliance, with basic knowledge of quality processes in clinical projects
Knowledge of Clinical Trial Management Systems (CTMS) and eTMF tools
Basic knowledge in SQL and Python
Power BI & Macros: Basic proficiency in Power BI dashboards and Excel macros
Time and Project management
Team Collaboration & Leadership
Platform: Udemy | Gained knowledge in ICH-GCP, clinical trial phases, eCRF design, DMP, MedDRA coding, CTMS, UAT, annotated CRF, data query management, and EDC tools like Rave and Veeva.
Platform: Udemy | Covered topics including ADRs, MedDRA, ICH guidelines, regulatory reporting, causality & seriousness assessment, narrative writing, vaccine vigilance, PV audits, and case processing.
STRS-2025 Award, American Association of Government College of Pharmacy Alumni, New York, USA
Research Publication:“Isolation of Bioactive Fraction from Psidium guajava (L) for In-VivoAnti-Fatigue Activity Using Exhaustive Swimming Test Method” published in the International Journal of Research Publication and Reviews, Vol. 6, Issue 7, July 2025. 🔗
I am deeply interested in roles that bridge science, medicine, and data—particularly in pharmacovigilance, clinical research, regulatory affairs, clinical data management, and medical writing These areas align with my passion for ensuring drug safety, improving clinical outcomes, and contributing to evidence-based healthcare My curiosity lies in understanding the regulatory frameworks that govern drug development and post-marketing surveillance, and how clinical data can be systematically collected, managed, and interpreted for better decision-making I enjoy working with scientific literature, summarizing complex data, and presenting it in a clear and compliant manner, which naturally drives my interest in medical and scientific writing I’m also motivated by the opportunity to contribute to clinical trial documentation, adverse event reporting, and regulatory submissions, ensuring patient safety and regulatory compliance These fields allow me to combine my background in pharmacy with analytical thinkin
• Clinical Data Management
• Medical Writing
• Regulatory affairs
• Healthcare Data Analyst
• Pharmacovigilance
• Clinical research