Associate Manager – Clinical Data Management
Location: Bangalore, Karnataka, India
Work Mode: Hybrid
Job ID: 2607042360W
Region: Asia Pacific – India
Industry: Clinical Research | Pharmaceuticals | Healthcare
Kenvue is a global leader in everyday health, built on more than a century of scientific heritage. Home to iconic brands such as NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID®, Kenvue is driven by science, innovation, and a strong commitment to improving lives worldwide. With a people-first culture and a global workforce of approximately 22,000 professionals, Kenvue empowers individuals to make a meaningful impact every day.
Kenvue is seeking an experienced Associate Manager, Clinical Data Management to join its Global Biostatistics, Data Management & Programming function in Bangalore. This role is responsible for end-to-end clinical data management activities for complex human research studies, ensuring high-quality, compliant, and timely delivery of clinical trial data.
Plan, manage, and oversee the design and execution of clinical data management activities for complex clinical research projects
Ensure all data management activities comply with GCP, ICH guidelines, CFR regulations, and internal SOPs
Collaborate with Data Management leadership to develop and maintain SOPs, standards, and best practices
Partner with Clinical Operations, Biostatistics, and other cross-functional teams to enhance data management processes and solutions
Deliver accurate, complete, and high-quality clinical trial data within defined timelines
Act as the primary point of contact for internal and external stakeholders for assigned studies
Provide oversight and quality governance for CROs, FSPs, and third-party vendors managing data deliverables
Lead EDC content development and integration with eCOA and external data systems
Enforce data standards, conventions, and quality expectations across studies
Contribute to the development and continuous improvement of data structure and data standards
Author, review, and maintain key data management documents including Data Management Plans (DMPs), Edit Check Specifications, and eCRF Completion Guidelines
Chair Data Quality Review meetings to ensure ongoing assessment of data accuracy, integrity, and completeness
Represent Clinical Data Management on cross-functional project and regulatory submission teams
Support health authority inspections, audits, and regulatory interactions
Evaluate proposals from external data management service providers
Mentor and guide junior data management professionals to support skill development and career growth
Manage end-to-end vendor oversight, monitor SLAs, and ensure data currency throughout the clinical trial lifecycle
Bachelor’s degree in Mathematics, Life Sciences, or a related scientific discipline
Minimum of 8 years of clinical data management experience within the pharmaceutical, biotech, or healthcare industry
Strong working knowledge of GCP, ICH guidelines, CFR, and industry-standard data management practices
Hands-on experience with Clinical Data Management Systems (CDMS/EDC platforms)
Proven ability to manage complex projects and analyze metrics for performance and quality reporting
Demonstrated experience working with cross-functional teams and external vendors
Excellent written and verbal communication skills, with the ability to engage senior management and global stakeholders
Strong leadership, organizational, and mentoring capabilities
At Kenvue, you will be part of a global organization that values innovation, collaboration, and scientific excellence. This role offers the opportunity to contribute to impactful clinical research programs while advancing your career in a dynamic, purpose-driven environment.
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