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:

• 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

Application Link