Associate Manager, Clinical Data Management

Posted An Hour Ago
Be an Early Applicant
17 Locations
In-Office or Remote
Senior level
eCommerce • Healthtech • Software
The Role
Manages end-to-end clinical data management for complex human-use research and clinical trial projects. Oversees data quality, EDC and other data collection systems, study documentation, vendors, CROs, and compliance with GCP, CFR, ICH, and company standards. Collaborates with Clinical, Biostatistics, external providers, and cross-functional teams; supports audits and health authority inspections; leads data quality reviews, evaluates proposals, manages deliverables, and mentors junior professionals.
Summary Generated by Built In

Kenvue is currently recruiting for a:

Associate Manager, Clinical Data Management

What we do

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. For more information, click here.

Role reports to:

Manager, Clinical Data Management

Location:

Asia Pacific, India, Karnataka, Bangalore

Work Location:

Hybrid

What you will do

Responsibilities will include but not limited to

• 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.

Skills Required

  • Bachelor's degree in Mathematics, Science, or a related field
  • At least 8 years of clinical data management experience in a healthcare-related industry
  • Ability to collaborate on multidisciplinary project teams and build productive relationships with external vendors
  • Sound knowledge of applicable CFR, GCP, and ICH guidelines and industry-standard data management practices
  • Proficiency with clinical data management systems
  • Strong project management skills
  • Expertise in metrics analysis and reporting methodologies
  • Strong oral and written communication skills
  • Ability to communicate effectively with senior management and cross-functional teams

Kenvue Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Kenvue and has not been reviewed or approved by Kenvue.

  • Fair & Transparent Compensation Pay is considered decent and competitive for the work performed. Base compensation combined with a solid benefits package supports a generally fair total rewards perception.
  • Healthcare Strength Comprehensive healthcare, life insurance, and disability plans are emphasized. Access to mental health resources and assistance programs further strengthens perceived health protection.
  • Parental & Family Support A global parental leave policy and support for adoption, fertility, and surrogacy are highlighted. These offerings contribute to a family‑friendly and supportive package for diverse families.

Kenvue Insights

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The Company
HQ: Summit, New Jersey
17,919 Employees
Year Founded: 2023

What We Do

Kenvue is the world’s largest pure-play consumer health company by revenue. Built on more than a century of heritage and propelled forward by science, our iconic brands — including Aveeno®, BAND-AID® Brand Adhesive Bandages, Johnson’s®, Listerine®, Neutrogena®, Tylenol® and Zyrtec® — are recommended by health care professionals and can be trusted by consumers who use our products to improve their daily lives. Our team members share a digital-first mindset, with an approach to innovation grounded in deep human insights and work every day to earn a place for our products in consumers’ hearts and homes. At Kenvue, we believe everyday care can not only make people well; it can make them whole. Beware of recruitment scams: https://www.kenvue.com/media/recruitment-scams-alert

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