Associate Manager, Clinical Data Management

Kenvue; Bengaluru; Hybrid; INR 1,800,000 - 2,400,000; Full time

Job summary

Kenvue seeks an Associate Manager, Clinical Data Management in Bengaluru with 8+ years in clinical data management. Hybrid work arrangement in India’s Karnataka region. You will lead DM activities, coordinate with cross-functional teams, and ensure data quality and timely delivery for complex trials.

The role requires strong project management, regulatory knowledge, and proficiency with CDMS. You will mentor junior staff and oversee vendor DM deliverables in a global setting.

Qualifications

• Bachelor's degree in Mathematics, Science or related field.
• 8+ years of clinical data management experience in healthcare industry.
• Proficiency with Clinical Data Management System; strong project management and communication skills.

Responsibilities

• Plans and manages the design and implementation of data management tasks for complex trials.
• Ensures all data management activities meet GCP, CFR, ICH guidelines and company procedures.
• Leads SOP and data standard development with data management team.
• Coordinates with Clinical and Biostatistics to improve DM solutions.
• Delivers complete, high-quality clinical trial data on time for assigned projects.
• Mentors junior professionals and maintains vendor oversight for DM deliverables.

Skills

Project management

Regulatory knowledge

CDMS proficiency

Written and verbal communication

Education

Bachelor's degree in Mathematics, Science or related field

Tools

Clinical Data Management System

Job description

Associate Manager, Clinical Data Management

At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent.

Who We Are

Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours.

Role Reports To

Manager, Clinical Data Management

Location

Asia Pacific, India, Karnataka, Bangalore

Work Location

Hybrid

What You Will Do

• Plans and manages the design and implementation of Data Management tasks for complex human use research activities to successfully achieve strategic objectives
• Ensures all Data Management activities are conducted in accordance with high ethical and quality standards, all applicable GCP regulations and company procedures
• Coordinate with Data Management lead in the development of SOPs and other data management standards
• Collaborates with other functions such as Clinical and Biostatistics in evaluating and/or implementing opportunities to improve Data Management solutions
• Efficiently plans, coordinates, and delivers complete, high quality and reliable clinical trial data in a timely manner for assigned projects
• Responsible for end-to-end clinical data management activities and serves as a primary point of contact for internal and external study team members with some oversight from senior data management resources
• Provides strong quality and project oversight over third party vendor responsible for data management deliverables
• Takes a leadership role to gather content and integration requirements for EDC and close collaboration with partners supporting other data collection systems (eCOA, External Data)
• Enforces data standard conventions and quality expectations for clinical data per defined processes
• Contribute to the definition of data structure standards; Authors, reviews/revises DM related study plans including Data Management Plan, Edit Check Specifications, eCRF Completion Guidelines and other study documents to ensure quality and standardization
• Chairs Data Quality Review meetings with cross functional study team members to ensure on-going review of clinical study data accuracy, quality and completeness
• Represents DM on cross-functional project teams & submission teams
• Provides support to Health Authority inspections and audits
• Represents Data Management on cross-functional project teams
• Evaluates proposals from external service providers
• Mentor junior professionals for skill set advancement
• FSP/CRO/Vendor Oversight: May act as core member of the study team and provides FSP/CRO/Vendor oversight for end-to-end Data Management activities, manages data currency throughout the trial, and overall monitoring DM deliverables according to the Service Level Agreement (SLA)

Required Qualifications

• Bachelor’s Degree in Mathematics, Science or a related field required
• At least 8 years of clinical data management experience in healthcare related industry
• Able to work collaboratively on multi-disciplinary project teams and develop productive relationships with external vendors
• Sound knowledge of all applicable regulations including CFR, GCP, ICH guidelines and industry standard practices regarding data management
• Proficiency with Clinical Data Management System required
• Strong project management; Exhibits expertise in metrics analysis and reporting methodologies
• Strong oral and written communication skills
• Communicate effectively with senior management and cross-functional teams

If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.