IQVIA, formerly Quintiles and IMS Health, Inc.,is an American multinational company serving the combined industries of health information technology and clinical research. It is a provider of biopharmaceutical development and commercial outsourcing services, focused primarily on Phase I-IV clinical trials and associated laboratory and analytical services, including consulting services. It has a network of more than 58,000 employees in more than 100 countries.As of 2017, IQVIA was reported to be one of the world's largest contract research organizations Job Overview We are seeking an experienced and detail-oriented Associate Lead Data Manager to oversee data management activities across multiple clinical projects. In this role, you will ensure high-quality data delivery in line with sponsor requirements, while collaborating with cross-functional teams, sites, and external partners. Key Responsibilities Gather study set-up requirements through effective communication with stakeholders. Lead database set-up, configuration, and validation to ensure optimal study design and data integrity. Support validation and implementation of new device integrations. Perform ongoing data cleaning activities to ensure accurate, timely, and high-quality deliverables. Ensure all outputs meet established quality standards and client expectations. Train and mentor new team members. Lead internal study meetings, participate in sponsor meetings, and support audits and study kick-offs. Track and manage project progress, identify risks, and implement corrective actions in collaboration with the Data Team Lead (DTL). Oversee database revisions and support the adoption of new technologies. Collaborate with programming teams to drive process improvements and automation initiatives. Ensure compliance with all required training and electronic SOPs (eSOPs). Contribute expertise to the development, review, and maintenance of standard operating procedures (SOPs) and work instructions. Maintain effective, collaborative communication with leadership, line managers, and cross-functional teams. Qualifications & Requirements Education: Master’s degree in Life Sciences / Postgraduate in Science / Bachelor of Pharmacy or equivalent preferred. Strong understanding of the drug development lifecycle and overall clinical research processes. Proficiency in English (spoken and written). Advanced skills in Microsoft Office applications (Excel, Word, Outlook). Strong analytical, organizational, and problem-solving abilities. Excellent communication and stakeholder management skills. Ability to manage multiple projects and meet deadlines in a fast-paced environment.