Specialist Data Acquisition Expert - eDC

Position Title: Specialist Data Acquisition Expert – eDC

Janssen Research and Development, L.L.C., a member of Johnson and Johnson's Family of Companies, is recruiting for a Specialist Data Acquisition Expert – eDC to join our Data Acquisition & Coding (DAC) team within Integrated Data Analysis and Reporting (IDAR) Data Management.

Position locations: Greater Mumbai, India; remote flexibility may be considered.

At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to build a world without disease. Redefining lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promising science. We are Janssen! We collaborate with the world for the health of everyone in it. Learn more at www.janssen.com and follow us @JanssenGlobal.

Diversity & Inclusion are crucial to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years. Regardless of your race, belief, sexual orientation, religion, or any other trait, YOU are welcome in all open positions!

Position Summary

Are you ready to join a growing team driving the implementation of data acquisition strategy and the future e-clinical trial landscape at Janssen R&D?!

As a key member of the DAC team, the Specialist Data Acquisition Expert – eDC, uses in-depth knowledge to provide trial-level support for the setup and management of Electronic Data Capture (eDC) systems and their related components and activities.

You will be empowered to lead a portfolio of trials of low to high complexity, across a variety of compounds, disease areas, or therapeutic areas.

The successful candidate will work in an agile, fast paced, team centric and evolving data environment applying creative problem-solving skills and relevant knowledge to support R&D innovation.

Key responsibilities

• Execute Data Acquisition responsibilities related to the setup and management of eDC systems for one or more trials of low to high complexity.
• Collaborate cross-functionally to understand the purpose of data collected and define trial level requirements related to eDC systems.
• Ensure correct adoption of clinical data standards to guarantee consistency across studies, compounds, disease areas, and therapeutic areas.
• Provide oversight on external partners performing data management activities on Janssen's behalf or execute the data management activities internally.

Actively contribute to the shaping of the organization, improving re-usability, efficiency, and consistency of DAC tools and processes across studies and therapeutic areas.