---
title: "Himani Lodhi - Business Associate in Jabalpur | Tal"
description: "Meet Himani Lodhi, B.Pharm (Hons) | ICH-GCP Certified | Clinical Research | CRC · Pharmacovigilance · Regulatory Affairs | Seeking Fresher Roles in CRO & Pharma based in Jabalpur."
image: "https://tal.club/meet/himani-lodhi/share-image"
---

# Himani Lodhi on Tal

## Headline

B\.Pharm \(Hons\) \| ICH\-GCP Certified \| Clinical Research \| CRC · Pharmacovigilance · Regulatory Affairs \| Seeking Fresher Roles in CRO & Pharma

## About

B\.Pharmacy \(Honors\) graduate from RGPV Jabalpur \(2025\) with a strong foundation in pharmaceutical sciences, drug regulatory affairs, GMP compliance, and clinical pharmacokinetics — actively seeking a Clinical Research Coordinator, Pharmacovigilance Associate, or Regulatory Affairs role in a CRO or pharmaceutical organization\. 🔬 PHARMACEUTICAL & RESEARCH BACKGROUND I completed a GMP\-certified internship at Daymark Pharmaceuticals where I performed in\-process quality checks and maintained batch documentation — building the protocol compliance and GDP documentation skills directly applicable to clinical trial site operations\. As a Business Associate at Atlantis Formulation Pvt\. Ltd\. \(May 2025–Feb 2026\), I managed pharmaceutical regulatory documentation, coordinated with healthcare professionals, and maintained structured compliance records — developing strong stakeholder communication and data management capabilities\. ✅ CERTIFICATIONS & SKILLS • ICH\-GCP E6\(R3\) Certified — freegcp\.com • GMP, SOP Adherence, ALCOA Documentation • CRF Management \| EDC Awareness \(Medidata Rave\) • Pharmacovigilance \| ICH E2 Series \| MedDRA Awareness • Drug Regulatory Affairs \| CDSCO \| NDCT Rules 2019 • MS Excel \(Advanced\) \| MS Word \| Data Management 🎯 WHAT I AM LOOKING FOR Entry\-level roles in: Clinical Research Coordinator \(CRC\) \| Clinical Trial Assistant \(CTA\) \| Pharmacovigilance Associate \| Clinical Data Associate \| Regulatory Affairs Assistant I am a quick learner, detail\-oriented, and deeply committed to patient safety and data integrity\. I am available immediately for remote or on\-site opportunities across India\. 📩 Open to opportunities — feel free to connect or message me directly\.

## Location

Jabalpur

## Work experience

Business Associate at Atlantis Formulations Pvt Ltd, May 2025 \- Feb 2026 · 10 mos, Jabalpur, • Applied pharmaceutical regulatory and product compliance knowledge to support clinical and commercial operations — building direct understanding of GMP, SOP adherence, and regulatory frameworks applicable to clinical trial site management\. • Maintained meticulous records of product interactions, compliance documentation, and operational data in MS Excel — reflecting the CRF data entry, audit trail, and source document standards required in clinical research\. • Coordinated with healthcare professionals to communicate complex pharmaceutical and regulatory product information — developing the stakeholder communication and investigator\-liaison skills essential for CRC and CRA roles\. • Conducted structured market analysis and competitor research using systematic data collection methodologies — directly applicable to clinical data gathering and protocol\-based evaluation in trial settings\. • Consistently met daily targets and KPIs across high\-volume, multi\-task operations — demonstrating the performance accountability required for clinical trial timelines and reporting deadlines\. Skills: GMP · SOP Adherence · MS Excel · Pharmaceutical Regulatory Affairs · Data Documentation · Stakeholder Communication Copy

Intern — Pharmaceutical Manufacturing, Quality Control & GMP ComplianceCopy at DAYMARK PHARMACEUTICALS \(INDIA\) PRIVATE LIMITED, Aug 2024 \- Sep 2024 · 2 mos, Jabalpur, Madhya Pradesh, India, • Performed GMP\-compliant in\-process quality checks and SOP monitoring in a licensed pharmaceutical manufacturing facility — developing the protocol compliance, quality verification, and documentation skills directly transferable to clinical trial site operations\. • Maintained batch records, quality control observation reports, and production documentation in accordance with Good Documentation Practices \(GDP\) — building data integrity and audit\-ready documentation habits essential in clinical research\. • Gained practical exposure to pharmaceutical regulatory frameworks, quality assurance workflows, and compliance verification — forming the foundation for understanding ICH\-GCP and CDSCO clinical trial regulatory requirements\. • Developed strong attention to detail, systematic evaluation approach, and zero\-tolerance mindset for documentation errors — core competencies for any clinical research coordinator role\. Skills: GMP · GDP · Quality Control · SOP · Batch Record Documentation · In\-Process Checks · Pharmaceutical Compliance

## Education

Bachelor's degree, Pharmacy, Shri Ram Institute of Technology \(RGPV\)

Higher Secondary, Physics,Chemistry,Biology, Hitkarini Higher Secondary School , Deoltal, Garha, Jabapur

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

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