Industrial Trainee
PADM Laboratories Research pvt. Ltd
Bengaluru, Karnataka
- Undergone industrial training in quality control and R&D department
Irayya Gurayya Mathapati
Bengaluru,Karnataka
Summary
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
Work History
Education
M-pharm - Pharmacognosy
Government College of Pharmacy
Bengaluru 02.2025 - 08.2025
B-pharmacy
Government College of Pharmacy
Bengaluru 08.2019 - 11.2023
Skills
- Basic knowledge about ICH, GCP and GLP guidelines
- Awareness of Adverse Drug Reaction (ADRs), AE/SE
- Familiar with the fundamentals of clinical trial design, trail phases and documentation
- Instrument troubleshooting and calibration
- Microsoft Excel (VLOOKUP, XLOOKUP, Pivot tables, conditional formatting)
- Microsoft Word
- Microsoft PowerPoint
- Basic data handling and spreadsheet
- Awareness of regulatory requirements and ethics in clinical trials
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
- Time management
- Adaptable to Ad-hoc Situations
- Data integrity and compliance
Certification
- Clinical data management Certification:
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.
- Pharmacovigilance Certification:
Platform: Udemy | Covered topics including ADRs, MedDRA, ICH guidelines, regulatory reporting, causality & seriousness assessment, narrative writing, vaccine vigilance, PV audits, and case processing.
- Certificate of Regulatory Affairs, Pharma State Academy
- GOOD CLINICAL PRACTICE, National Institute on Drug Abuse-Clinical Trials Network (NIDA)
- Introduction to the Principles and Practice of Clinical Research 2024-2025 by NIH (National institute of health)
Accomplishments
- Qualified GPAT-2023
- Qualified NIPER-2023
- Secured 70 rank in Karnataka PG CET-2023
- President (2024) and Sports secretary (2023) of pharmaceutical society of Government college of Pharmacy Bengaluru
Educational Endeavors
- M-pharm project, Bioactivity guided fractionation of Psidium guajava leaves for in vivo anti fatigue activity by exhaustive swimming test model.
- B-pharm project, A comparative study of cox-1 and cox-2 inhibitors in chronic inflammation, a review on clinical evidence.
- Industrial training, Undergone industrial training at 'PADM Laboratories Research pvt. Ltd' Bengaluru in quality control and R&D department.
Recognition
STRS-2025 Award, American Association of Government College of Pharmacy Alumni, New York, USA
Timeline
M-pharm - Pharmacognosy
Government College of Pharmacy
02.2025 - 08.2025
B-pharmacy
Government College of Pharmacy
08.2019 - 11.2023
Industrial Trainee
PADM Laboratories Research pvt. Ltd
Work Availability
monday
tuesday
wednesday
thursday
friday
saturday
sunday
morning
afternoon
evening
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Work Preference
Work Type
Full TimeLocation Preference
On-SiteRemoteHybridImportant To Me
Career advancementCompany CulturePersonal development programsWork from home optionQuote
There is a powerful driving force inside every human being that, once unleashed, can make any vision, dream, or desire a reality.
Tony Robbins
Languages
English
Bilingual or Proficient (C2)
Hindi
Bilingual or Proficient (C2)
kannada
Bilingual or Proficient (C2)
Telugu
Elementary (A2)
publications
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. 🔗
Interests
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
interested roles
• Clinical Data Management
• Medical Writing
• Regulatory affairs
• Healthcare Data Analyst
• Pharmacovigilance
• Clinical research