SNEHA VARSHINI VAASIKARLA

Detail-oriented and highly motivated healthcare professional with a strong foundation in pharmaceutical sciences and healthcare data practices. Skilled in quality assurance principles, Good Manufacturing Practices (GMP), and pharmaceutical analysis. Adept at interpreting laboratory data, maintaining documentation accuracy, and ensuring compliance with regulatory standards. Committed to upholding product quality, patient safety, and continuous improvement in pharmaceutical operations.

• Awarded Best Office Bearer for exemplary contributions to the Indian Pharmaceutical Association – Student Forum (IPA-SF), 2022–2023.
• Secured 1st Prize in an E-poster competition at St. Peter’s Institute of Pharmaceutical Sciences.
• Won 1st Prize in a national-level poster presentation on converting blood groups to universal donors using enzymatic methods.

• Python Programming – Gained foundational and applied knowledge of Python for data analysis and automation.
• SQL for Data Analysis – Acquired skills in querying, joining, and analyzing datasets using SQL.
• HIPAA Compliance Training – Familiar with privacy, security rules, and healthcare data protection protocols.
• ICH-GCP (Good Clinical Practice) – Understanding of international standards for ethical clinical research.
• ICD-10 Coding and Classification – Knowledge of medical coding practices for disease classification and reporting.

Doctor of Pharmacy (PharmD):

• Pharmaceutical Analysis: Analytical techniques for drug testing and quality assurance.
• Pharmaceutics: Formulation and manufacturing processes of pharmaceutical products.
• Pharmaceutical Microbiology: Microbial testing methods critical to product safety.
• Pharmaceutical Jurisprudence: Regulatory standards and compliance in the pharmaceutical industry.
• Biostatistics and Research Methodology: Statistical analysis for quality testing and validation.
• Clinical Pharmacy: Medication safety and therapeutic drug monitoring.
• Pharmaceutical Inorganic and Organic Chemistry: Chemical properties and reactions relevant to raw material and finished product testing.
• Medicinal Chemistry: Structure-activity relationships critical for understanding drug purity and potency.
• Pharmaceutical Formulations: Preparation and stability of dosage forms.
• Biopharmaceutics and Pharmacokinetics: Drug absorption and bioavailability testing principles.
• Hospital Pharmacy: Dispensing practices and compliance with hospital quality standards.

Master of Science in Information Science – Health Informatics Concentration:

• Medical Informatics: Understanding of healthcare systems and digital tools in pharmaceutical settings.
• Information and Cyber Security: Safeguarding sensitive quality and compliance data.
• Legal & Ethical Issues in Health Informatics: Comprehension of legal and ethical aspects of pharmaceutical data handling.
• Health Data Analytics: Analytical approaches for process improvement and quality monitoring.
• Research Methods and Analysis: Structured methods for experimental design and data analysis