Are you looking to advance your career in clinical data management with a leading global CRO? IQVIA is hiring a Clinical Data Management Lead in Pune, India. This full-time role offers you the chance to oversee end-to-end data management delivery for clinical trials, ensuring quality, compliance, and on-time execution. With a strong focus on leadership and project management, this role is perfect for professionals with 3–4 years of CDM experience who are ready to take the next step.
🔑 Key Responsibilities
As a Clinical Data Management Lead, you will:
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- Manage end-to-end data management services for single/multi-service projects.
- Gather study setup requirements and support new device integrations.
- Oversee data cleaning activities to ensure accuracy and compliance.
- Track project progress, identify risks, and apply corrective measures.
- Lead internal study meetings, audits, and sponsor communications.
- Provide training and mentorship to new joiners.
- Collaborate with programming teams for process innovation and automation.
- Ensure adherence to SOPs, regulatory standards, and project timelines.
🎓 Required Qualifications
To be eligible, you should have:
- Bachelor’s degree (Pharmacy or equivalent preferred).
- 3–4 years of direct data management experience, including 1 year as a CDM project lead.
- Advanced knowledge of the drug development lifecycle and clinical research processes.
- Strong skills in MS Excel, Word, and data systems.
- Excellent communication and leadership abilities.
💡 Why Join IQVIA?
At IQVIA, you’ll be part of a global leader in clinical research and healthcare analytics. Benefits include:
- Exposure to cutting-edge clinical trial technologies.
- Opportunity to lead cross-functional teams.
- Professional development and training programs.
- A collaborative, innovation-driven work culture.
📌 How to Apply
