---
title: "Dr. Hepsiba Pusala - Clinical Research Coordinator in Guntur | Tal"
description: "Meet Dr. Hepsiba Pusala, Clinical Research Coordinator | PharmD | ICH-GCP | Clinical Trials, Informed Consent, Source Documentation, Scientific Writing based in Guntur."
image: "https://tal.club/meet/dr-hepsiba-pusala/share-image"
---

# Dr\. Hepsiba Pusala on Tal

## Headline

Clinical Research Coordinator \| PharmD \| ICH\-GCP \| Clinical Trials, Informed Consent, Source Documentation, Scientific Writing

## About

Clinical Research Coordinator with a PharmD background and 2\.11 years of experience supporting clinical trials in accordance with ICH\-GCP, protocol requirements, and regulatory standards\. Experienced in patient recruitment, informed consent, study coordination, source documentation, CRF review, and data quality support in hospital\-based research settings\. I collaborate with investigators, site teams, and healthcare professionals to support compliant study execution and accurate trial documentation\. My background in clinical pharmacy adds strong exposure to drug safety, ADR identification, patient counseling, and pharmacology, which strengthens my work across clinical research and patient\-focused documentation\. I am also building my profile in scientific and medical writing, with strengths in literature review, clinical data interpretation, and clear scientific communication\. I am targeting roles in Clinical Research, CRA\-track functions, Medical Writing, Pharmacovigilance, and related life sciences domains\.

## Location

Guntur

## Work experience

Clinical Research Coordinator at Aditya Multispeciality Hospitals, Oct 2023 \- Present · 2 yrs 11 mos, ●Support the conduct of clinical trials in accordance with ICH\-GCP, study protocols, and regulatory requirements\. ●Coordinate patient recruitment, screening, and informed consent procedures to support study enrollment and retention\. ●Maintain and review source documentation, CRFs, and study records for accuracy, completeness, and protocol compliance\. ●Liaise with investigators, site staff, and study teams to coordinate study visits, follow\-up activities, and trial\-related documentation\. ●Support data review, query resolution, and documentation readiness for monitoring and audit requirements\. ●Contribute to participant safety oversight through timely documentation of adverse events / clinical observations, where applicable\.

Clinical Pharmacist Intern at Area hospital, Aug 2022 \- Jul 2023 · 1 yr, Narasaraopeta, ● Participated in multidisciplinary ward rounds across General Medicine, Pediatrics, Orthopedics, and Obstetrics & Gynecology\. ● Identified adverse drug reactions, drug interactions, and medication\-related risks and communicated findings to clinicians\. ● Provided drug information and patient counseling to support safe and effective medication use\. ● Strengthened clinical understanding of patient safety, pharmacotherapy, and healthcare documentation relevant to research and pharmacovigilance\.

## Education

Doctor of Pharmacy \- PharmD, Pharmacology, Narasaraopeta Institute of Pharmaceutical Sciences, Kotappakonda Road, Yellamanda \(P\.O\), Narasaraopet \(Md\) PIN\- 522 601,\(CC\-CD\)

Intermediate, Sri Chaitanya College of Education

[View the original profile](https://tal.club/meet/dr-hepsiba-pusala)

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