WhatsApp Group
Join Now
WhatsApp Channel
Join Now
Telegram Group
Join Now

Advertisement

IQVIA Hiring Clinical Data Management | Multiple Locations

Published on

IQVIA

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences or equivalent

Kochi, Kolkata, Thane, Bangalore, Hyderabad

2.5 years

Verified Job

Email Application
Advertisement

IQVIA, a global leader in clinical research, analytics, and healthcare intelligence, is inviting experienced Clinical Data Management (CDM) professionals to join its growing India operations. This opportunity is ideal for candidates with hands-on experience in core clinical data management, Medidata Rave EDC, and end-to-end clinical trial execution.

If you are passionate about clinical research data integrity, regulatory compliance, and working on global trials in a hybrid work environment, this IQVIA job opening can be a significant step in your clinical research career.


๐Ÿงช Job Overview โ€“ Clinical Data Management at IQVIA

  • Company: IQVIA
  • Job Role: Clinical Data Management Professional
  • Employment Type: Full-time
  • Work Model: Hybrid (2โ€“3 days/week office-based)
  • Locations: Kochi, Kolkata, Thane, Bangalore, Hyderabad
  • Experience Required: 2.5+ years
  • Industry: Clinical Research / CRO

๐Ÿงพ Key Responsibilities

  • Manage end-to-end Clinical Data Management activities including study start-up, conduct, and close-out
  • Design, review, and maintain CRFs and EDC databases using Medidata Rave
  • Perform data validation, discrepancy management, and query resolution
  • Ensure compliance with ICH-GCP, SOPs, and regulatory guidelines
  • Support data lock, interim analysis, and database close-out activities
  • Collaborate with cross-functional teams including Clinical Operations, Biostatistics, and Medical Writing
  • Participate in audits and inspections as required

๐ŸŽ“ Required Qualifications & Skills

  • Minimum 2.5 years of experience in Core Clinical Data Management
  • Strong hands-on expertise in Medidata Rave EDC
  • Exposure to study start-up, conduct, and close-out phases
  • Solid understanding of clinical trial lifecycle and CDM processes
  • Willingness to work in shifts based on trial requirements
  • Excellent communication and documentation skills

Preferred Backgrounds:
B.Pharm, M.Pharm, Pharm.D, MSc Life Sciences, or equivalent clinical research qualification.

Advertisement

๐Ÿ’ผ Why Join IQVIA?

  • Work with a global CRO leader in innovative clinical research
  • Exposure to international clinical trials and advanced technologies
  • Hybrid working model supporting workโ€“life balance
  • Strong learning, career progression, and internal mobility
  • Inclusive, collaborative, and research-driven work culture

๐Ÿ’ฐ Salary & Compensation

  • Estimated Salary Range: โ‚น6,00,000 โ€“ โ‚น10,00,000 per annum (CTC)
    (Final compensation will depend on experience, skills, and location)

๐Ÿ“ Job Locations

  • Kochi
  • Kolkata
  • Thane (Mumbai Metropolitan Region)
  • Bangalore
  • Hyderabad

๐Ÿ“ฉ How to Apply

Interested and eligible candidates should send their updated CV to:

๐Ÿ“ง Email: vaishnavinandkishor.kamble@iqvia.com

Tip: Mention โ€œClinical Data Management โ€“ Pharmabharatโ€ in the email subject for better visibility

Application Link

IQVIA Hiring Clinical Data Management | Multiple Locations
Advertisement

Share This Job

โœ… Job Copied Successfully!

Ad Popup