Mahbubnagar, Telangana, India
I am a Pharm.D graduate with a strong foundation in Clinical Research, Clinical Data Management, Pharmacovigilance, Medical Writing, and Regulatory Affairs. My academic journey, combined with hands-on internship experiences in hospital settings, has equipped me with a deep understanding of drug safety, patient care, and research methodologies. During my research project on the Prevalence of Anaemia in Type-2 Diabetes Mellitus and Its Associated Risks, I processed 210 subjects' Informed Consent Forms (ICFs) and Case Report Forms (CRFs) to derive meaningful insights. Working closely with my Clinical Guide, I conducted statistical analysis to generate significant results that highlighted the impact of anaemia on cardiovascular, renal, and neuropathic complications in T2DM patients. With a passion for data-driven decision-making and healthcare innovation, I am eager to contribute to the pharmaceutical industry in roles related to clinical research, data management, and drug safety.
• Participated in a 45-day structured internship covering Clinical Research, ICH-GCP, Pharmacovigilance (ICSRs), Clinical Data Management activities, Scientific Writing, and Regulatory Affairs. • Gained hands-on exposure to concepts like CRF/ICF handling, SAE reconciliation, dossier compilation, and eCTD modules. • Developed understanding of compliance workflows and documentation across CDM, CR, and PV domains.
Provided emergency care, patient treatment, ICU monitoring, and surgical profiling, while ensuring seamless collaboration, medical documentation, and patient education. Conducted ward rounds, medication safety assessments, and patient counseling, utilizing pharmaceutical databases and improving nursing practices through an IM injection guide.