IQVIA Hiring Freshers – Trainee Clinical Data Coordinator Job in Kochi | Clinical Data Management 2026

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IQVIA Hiring Freshers – Associate Trainee Clinical Data Coordinator | Kochi | 2026

IQVIA
Kochi
Freshers Only
Clinical Data Management
Onsite
Full-Time

📄 About the Company

IQVIA is a global leader in clinical research, healthcare analytics, and life sciences consulting. The company supports pharmaceutical, biotech, and medical device organizations worldwide by delivering advanced analytics, technology solutions, and clinical research services.

IQVIA is known for its strong training programs, global exposure, and structured career growth in Clinical Research & Clinical Data Management (CDM).

📌 Job Overview

IQVIA is hiring Associate Trainee Clinical Data Coordinators for its Kochi, Kerala office.

This is a fresher-only, entry-level role designed for candidates who want to start their career in Clinical Data Management and gain hands-on experience working on global clinical trials.

Candidates with any prior PF (Provident Fund) account are NOT eligible for this role. This condition is strictly applicable.

🧪 Job Details – Associate Trainee Clinical Data Coordinator

Company: IQVIA

Position: Associate Trainee Clinical Data Coordinator

Location: Kochi, Kerala

Work Mode: Onsite (Office-based)

Experience: 0–1 Year (Freshers Only)

PF Account: ❌ Candidates with PF account are NOT eligible

Employment Type: Full-Time, Permanent

Shift Timings:

  • 5:00 AM – 2:00 PM
  • 2:00 PM – 11:00 PM

(Rotational shifts may apply based on business requirements)

🧾 Key Responsibilities

  • Accurately enter clinical trial data into Clinical Data Management Systems (CDMS)
  • Perform data entry, scanning, indexing, and document tracking activities
  • Process study-related documents as per CRF Tracking & Data Entry Guidelines
  • Support maintenance of Data Management Study Files
  • Assist in data review, discrepancy management, and query resolution
  • Perform quality checks to ensure data accuracy and completeness
  • Follow Standard Operating Procedures (SOPs) and work instructions
  • Ensure compliance with ICH-GCP and regulatory requirements
  • Collaborate with team members to meet project timelines

🎓 Eligibility & Educational Qualifications

  • B.Pharm / M.Pharm / Pharm.D
  • BSc / MSc – Life Sciences
  • High School Diploma (minimum requirement as per IQVIA JD)
  • Freshers or candidates with relevant internship / training experience
  • Basic understanding of clinical research terminology preferred

🧠 Required Skills

  • Strong attention to detail and data accuracy
  • Good computer proficiency (MS Excel, documentation tools)
  • Basic understanding of clinical trial processes
  • Good communication and organizational skills
  • Ability to follow SOP-driven processes
  • Team-oriented and professional work ethic

💰 Salary & Benefits

  • ₹2,80,000 – ₹4,50,000 per annum (Estimated)
  • Structured training and onboarding
  • Hands-on exposure to global clinical trials
  • Career growth opportunities in CDM
  • Work with a globally recognized CRO
📌 Note Before You Apply:
We use a 15-second timer to encourage candidates to read the entire job description carefully before applying. Please ensure you meet the fresher & no-PF-account eligibility condition before proceeding.

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