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Associate Manager, Clinical Data Management

Kenvue
Kenvue
8 years
preferred by company
10 Jan. 30, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Associate Manager – Clinical Data Management
Location: Bangalore, Karnataka, India
Employment Type: Full Time | Hybrid
Job ID: 2607042360W
Industry: Clinical Data Management | Life Sciences | Healthcare


About Kenvue

Kenvue is a global leader in healthcare, built on over a century of heritage and rooted in science. Our portfolio includes iconic brands such as NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S®, and BAND-AID®, trusted by millions worldwide. We are driven by science, innovation, and a commitment to improving patient outcomes, creating products that matter every day.

Our global team of ~22,000 professionals thrives in a culture where every voice matters, and every contribution is valued. At Kenvue, you have the opportunity to impact millions of lives through clinical excellence, collaborative innovation, and leadership in data-driven healthcare solutions.


Role Overview

Kenvue is hiring an Associate Manager, Clinical Data Management to lead and oversee clinical data operations for complex human-use research projects. This position requires 8+ years of experience in clinical data management within the healthcare or life sciences industry and offers a hybrid work model in Bangalore, India.

The Associate Manager will ensure the accuracy, quality, and compliance of clinical trial data while collaborating with cross-functional teams and external vendors. This role provides leadership in data integration, standardization, and project execution for global clinical programs.


Key Responsibilities

Clinical Data Management & Oversight

  • Plan, manage, and implement data management tasks for complex clinical trials to achieve strategic objectives

  • Ensure all activities comply with GCP, ICH guidelines, CFR regulations, and internal SOPs

  • Coordinate with Data Management leads to develop SOPs, standards, and best practices

  • Deliver high-quality, reliable clinical trial data on schedule for assigned projects

Cross-Functional Collaboration

  • Collaborate with Clinical, Biostatistics, and other teams to optimize data management solutions

  • Serve as primary point of contact for internal and external study team members

  • Represent Data Management on cross-functional project teams and submissions

Vendor & Project Management

  • Provide oversight of third-party vendors (FSP/CRO) to ensure adherence to Service Level Agreements (SLA)

  • Evaluate external vendor proposals and maintain project accountability

  • Manage end-to-end data management activities, including EDC and other data collection systems (eCOA, External Data)

Data Quality & Standardization

  • Enforce data standards and quality expectations across clinical studies

  • Author, review, and revise Data Management Plans, Edit Check Specifications, eCRF Completion Guidelines, and related study documents

  • Chair Data Quality Review meetings to ensure accuracy, completeness, and compliance

  • Support Health Authority inspections and audits

Mentorship & Team Development

  • Mentor junior data management professionals to strengthen team skills and capabilities

  • Drive continuous improvement initiatives in clinical data processes and systems


Required Qualifications & Skills

  • Bachelor’s Degree in Mathematics, Science, or a related field

  • Minimum 8 years of experience in clinical data management in healthcare or life sciences

  • Proficiency with Clinical Data Management Systems (CDMS)

  • Strong knowledge of regulatory requirements (GCP, ICH, CFR) and industry best practices

  • Demonstrated project management skills with expertise in metrics, analysis, and reporting

  • Excellent written and verbal communication skills; able to collaborate effectively with senior management and cross-functional teams

  • Ability to work independently and manage complex projects while mentoring team members


Why Join Kenvue

Kenvue offers the opportunity to advance your career in a global, collaborative, and innovation-driven environment. Employees benefit from professional growth, leadership development, and the chance to impact healthcare outcomes on a global scale.


Apply now on ThePharmaDaily.com to join Kenvue as an Associate Manager – Clinical Data Management and be part of a team shaping the future of global healthcare.