---
title: "Pallavi Babar - Clinical Research Coordinator in Pune City | Tal"
description: "Meet Pallavi Babar, Clinical Data Management & Drug Safety | B.Pharm | CRC Experience | Medidata Rave, Oracle Clinical, MedDRA, ICH-GCP E6(R3) | Seeking CDM/Pharmacovigilance Roles at CROs based in Pune City."
image: "https://tal.club/meet/pallavi-26/share-image"
---

# Pallavi Babar on Tal

## Headline

Clinical Data Management & Drug Safety \| B\.Pharm \| CRC Experience \| Medidata Rave, Oracle Clinical, MedDRA, ICH\-GCP E6\(R3\) \| Seeking CDM/Pharmacovigilance Roles at CROs

## About

B\.Pharm graduate with hands\-on experience as a Clinical Research Coordinator and formal training in Clinical Data Management and Pharmacovigilance\. Skilled in EDC systems \(Medidata Rave, Oracle Clinical\), CRF/ISF documentation, source data verification, and query resolution, with working knowledge of MedDRA coding, ICSR processing, and AE/SAE reporting under ICH\-GCP E6\(R3\)\. Transitioning into Clinical Data Management / Safety Science Analyst roles at CROs, where I can apply my attention to detail, data quality mindset, and regulatory awareness to support clean, audit\-ready clinical trial data\. Open to: Clinical Data Associate \| Clinical Data Management Trainee \| Pharmacovigilance/Drug Safety Associate \| Safety Science Analyst

## Location

Pune City

## Work experience

Clinical Research Coordinator at Pulse Multispeciality Hospital, Jan 2026 \- Present · 7 mos, Pune, Maharashtra, India, Coordinate and support clinical trials in compliance with study protocols, ICH\-GCP guidelines, and regulatory requirements • Assist in patient screening, recruitment, and informed consent process • Maintain accurate source documents, CRFs, and Investigator Site File \(ISF\) • Ensure proper documentation and timely data entry • Monitor and report Adverse Events \(AEs\) and Serious Adverse Events \(SAEs\) as per protocol • Support Ethics Committee submissions and regulatory documentation • Coordinate with investigators, sponsors, and study teams for smooth trial conduct • Ensure patient safety, data quality, and protocol adherence

Clinical Research Coordinator at Sahyadri Hospitals, Oct 2025 \- Dec 2025 · 3 mos, On\-site

Clinical Research Coordinator at Sahyadri Hospitals, Oct 2025 \- Dec 2025 · 3 mos, Pune, Maharashtra, India

## Education

Mitcon biotechnology and pharmaceutical centre

Bachelor of Pharmacy \- BPharm, Pharmacy, Smt kashibai navale college of pharmacy

[View the original profile](https://tal.club/meet/pallavi-26)

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