🏷️ Job Title:
Manager, Clinical Data Management (CDM)
Job ID: R1491546
Location: Bengaluru, India (Hybrid)
Employment Type: Full-time
Job Available in Additional Locations
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🧭 Job Overview
Manage the end-to-end delivery of data management services for single or multi-service clinical projects with minimal supervision. Ensure quality deliverables are completed on time, within budget, and to customer satisfaction. Act as the Data Team Lead (DTL), providing technical and project leadership, as well as operational oversight and stakeholder communication.
🔍 Key Responsibilities
📊 Project & Data Oversight
Gather study setup requirements through communication with stakeholders.
Lead and/or oversee validation of device integrations with minimal supervision.
Perform and oversee regular data cleaning activities to ensure high-quality and timely deliverables.
Monitor project timelines and deliverables against contractual obligations (SOW).
👥 Leadership & Team Support
Provide training support to new team members.
Lead internal study meetings and represent the team in sponsor meetings (e.g., Study Kick-Offs, audits).
Support the implementation of new technologies, tools, and database revisions.
Collaborate with programming teams for process innovation and automation.
🔄 Process & Compliance
Ensure compliance with internal training, eSOPs, and documentation requirements.
Review, revise, and contribute to operational SOPs and work instructions.
Communicate effectively and collaboratively with line managers and cross-functional teams.
Proactively track and manage project progress, identify risks, and recommend corrective actions.
📋 Additional Duties
Perform other tasks and responsibilities as assigned by the Line Manager.
📚 Required Qualifications
Education:
Bachelor’s degree in Health, Clinical, Biological, Mathematical Sciences, or related field.
Experience:
3–4 years of direct Clinical Data Management (CDM) experience.
Minimum 1 year of experience as a CDM project lead. (Preferred)
🧠 Skills & Competencies
Strong understanding of the clinical research process and drug development lifecycle.
Proficiency in Microsoft Office tools: Excel, Word, Email, etc.
Excellent communication skills in English (spoken and written).
Knowledge of data validation, data cleaning, and study build processes.
Ability to manage multiple projects while maintaining quality and timelines.
Strong problem-solving and decision-making skills.
🏢 About IQVIA
IQVIA is a global leader in clinical research, data analytics, and healthcare intelligence. Our mission is to accelerate innovation in life sciences to improve patient outcomes and public health.
🔗 Learn more: https://jobs.iqvia.com
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