Roles & Responsibilities
• Lead end-to-end Clinical Data Management (CDM) activities for single or multi-service clinical studies
• Gather and analyze study setup requirements in collaboration with sponsors and internal stakeholders
• Oversee data collection, data cleaning, validation, and database lock activities
• Validate and manage new device and system integrations with minimal supervision
• Ensure all study deliverables meet sponsor expectations, quality standards, and timelines
• Track project progress, identify risks and issues, and implement corrective and preventive actions
• Lead study kick-off meetings, internal team meetings, and sponsor audits
• Support onboarding and training of new team members
• Collaborate with programming and technology teams to drive automation and process improvements
• Contribute to the development, review, and maintenance of SOPs and work instructions
Qualification
• B.Pharm / M.Pharm / Pharm.D / BSc / MSc in Life Sciences, Health Sciences, Clinical, Biological, Mathematical Sciences, or related discipline
Experience
• 3-4 years of clinical data management experience
• Minimum 1 year of experience as a CDM Project Lead preferred
Skills
• Strong understanding of the drug development lifecycle and overall clinical research process
• Hands-on expertise in clinical data collection, validation, and reporting
• Proficiency in Microsoft Excel, Word, and Outlook
• Strong spoken and written English communication skills
• Good leadership, problem-solving, and stakeholder management skills
• Ability to manage multiple priorities and meet project timelines
About the Company
IQVIA is a global leader in clinical research, healthcare analytics, and life sciences intelligence, supporting pharmaceutical, biotechnology, and healthcare organizations worldwide through advanced analytics, technology-enabled solutions, and deep scientific expertise to improve patient outcomes and accelerate innovation.