PHARMA BHARAT
PHARMACEUTICAL JOB PORTAL
No new notifications

Advertisement

Clinical Research Coordinator Job at IQVIA

Published on

IQVIA

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences, Clinical Research

Bangalore

3+ years

Verified Job

Online Application
Advertisement

Looking to build a career in clinical research jobs in India? IQVIA is hiring a Clinical Research Coordinator (CRC) in Bangalore. This opportunity is ideal for candidates with experience in clinical trials, patient data management, and Good Clinical Practice (GCP).

As a global CRO, IQVIA offers strong exposure to clinical operations, regulatory compliance, and patient safety, making this role a strategic entry or growth position in clinical research careers.


๐Ÿงช Job Overview

  • Position: Clinical Research Coordinator
  • Company: IQVIA
  • Location: Bangalore, India
  • Experience: 3+ years (clinical/medical setting)
  • Employment Type: Full-Time
  • Salary: โ‚น3.5 โ€“ โ‚น6 LPA (estimated industry range)
  • Last Date to Apply: April 4, 2026

๐Ÿ”‘ Key Responsibilities

  • Support investigators in executing clinical trials as per protocol and GCP
  • Review study protocols, CRFs, and EDC systems
  • Handle patient recruitment, screening, and consent process
  • Schedule and conduct study visits and procedures
  • Collect, record, and maintain clinical trial data with high accuracy
  • Manage lab samples, logistics, and testing processes
  • Monitor patient safety and adverse events reporting
  • Assist in data quality checks and query resolution
  • Prepare for audits, monitoring visits, and regulatory inspections
  • Train site staff on study protocols and compliance requirements

๐ŸŽ“ Qualifications

  • Bachelorโ€™s Degree (Life Sciences preferred) OR relevant diploma
  • 3+ years of experience in clinical research / healthcare setting
  • Strong knowledge of:
    • Good Clinical Practice (GCP)
    • Clinical trial processes
    • Regulatory documentation
  • Hands-on experience with clinical procedures (ECG, spirometry, etc.)
  • Proficiency in MS Office (Word, Outlook, Access)
  • Excellent communication and interpersonal skills

๐Ÿ’ผ Benefits

  • Work with a leading global CRO (IQVIA)
  • Exposure to international clinical trials and protocols
  • Strong career pathway into CRA, Clinical Operations, or Project Management
  • Training in regulatory compliance and audit readiness
  • Competitive salary and professional growth

๐Ÿ“ฉ Application Process

Application Link

Advertisement

Share This Job

โœ… Job Details Copied!
Ad Popup