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