Summary
Overview
Timeline
Work History
Education
Skills
Projects
Certification
Languages
Interests
Generic
Sathvika Aepura

Sathvika Aepura

Hyderabad

Summary

Motivated and detail-oriented Pharm.D. graduate seeking a challenging role in pharmacovigilance or clinical research to apply my knowledge of drug safety, clinical trial coordination. Eager to contribute to patient-centered research and enhance drug development processes by leveraging my skills in AE/SAE reporting, case processing, ICH-GCP adherence, and scientific analysis. Committed to maintaining high ethical standards, data integrity, and cross-functional collaboration in dynamic healthcare environments.

Overview

1
1
year of professional experience
3
3
Certification

Timeline

Pharm-D Intern

Kamineni Hospitals
06.2024 - Current

Doctor of Pharmacy (Pharm-D) -

Samskruthi College of Pharmacy

Work History

Pharm-D Intern

Kamineni Hospitals
06.2024 - Current
  • Assisted in pharmacovigilance activities, including monitoring adverse drug reactions (ADRs) and maintaining safety databases in compliance with regulatory standards.
  • Conducted an observational study on the use of diuretics in oliguric acute kidney injury, contributing to data interpretation and study outcomes.
  • Collaborated with healthcare professionals on medication safety, patient counseling, and drug therapy monitoring, improving patient outcomes and therapeutic efficacy.
  • Participated in clinical trials, supporting patient recruitment, data collection, and analysis of clinical outcomes in accordance with GCP guidelines.
  • Assisted in study interventions, adverse event monitoring, and clinical documentation to ensure trial accuracy and compliance.
  • Contributed to scientific publications and research reports, supporting manuscript preparation and data-driven writing.

Education

Doctor of Pharmacy (Pharm-D) -

Samskruthi College of Pharmacy
06-2025

Skills

  • Clinical Trial Monitoring
  • Adverse Event (AE) & Serious Adverse Event (SAE) Reporting
  • Case Processing & Safety Data Entry
  • Knowledge of ICH-GCP Guidelines
  • MedDRA
  • Patient Counseling
  • Clinical Data Management
  • Protocol and Informed Consent Form Review
  • Medical case summarization
  • Clinical Study Report (CSR)
  • Scientific Literature Review
  • Medical Terminology Proficiency
  • Attention to Detail and Analytical Thinking
  • MS Office (Word, Excel, PowerPoint)

Projects

Title:Observational Study On Role Of Diuretics In Oliguric Acute Kidney Injury

  • Conducted a hospital-based observational study involving 120 patients to assess the clinical outcomes of loop diuretic therapy in oliguric AKI, focusing on fluid overload management and renal function recovery.
  • Collaborated with a multidisciplinary healthcare team to collect and interpret patient data, analyze laboratory parameters, and evaluate quality of life outcomes.
  • Utilized SPSS for statistical analysis to ensure evidence-based conclusions and enhance clinical relevance.
  • Gained hands-on experience in clinical research methodology, patient interaction, ethical compliance, and data-driven decision-making in a hospital setting.

Certification

  • Data Management for Clinical Research
  • Good Clinical Practice (GCP) Certification
  • MedDRA

Languages

  • English
  • Telugu
  • Hindi

Interests

Learning New Technologies

Music

Dance

Sathvika Aepura