Associate Manager, Clinical Data Management

Description

Kenvue is currently recruiting for:

Associate Manager, Clinical Data Management This position is based at Bangaloe .

Who We Are

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.

Our global team is made up with 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers.

With expertise and empathy, being a Kenvuer means to have the power to impact life of 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 .

What You Will Do

Job Responsibilities:

• Plans and manages the design and implementation of Data Management tasks for complex human use research activities in order 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 minimal 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 ...