Global Data Manager (1 of 6)

Johnson & Johnson is currently seeking a Global Data Manager.

This position can be located in Spring House, PA; Titusville, NJ; or Raritan, NJ.

At Johnson & Johnson,we believe health is everything.

Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.

Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

Learn more at https://www.jnj.com.

For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.

Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.

Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.

We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve.

Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.

At Johnson & Johnson, we all belong.

The Global Data Manager (GDM) is a professional individual contributor role at entry level that will provide oversight and accountability and/or execute data management activities and/or perform scientific data review for one or more trials of low to moderate complexity.

The GDM will make recommendations and influence decisions for specific trials or assignments.

This individual Will analyze and provide input into decisions with direction from a manager or Data Management Leader (DML).

This position receives ongoing direction to achieve objectives, and work is reviewed on a regular basis with the DML.

Principal Responsibilities:


* Work with external suppliers, trial customers and other internal/external partners to establish, align and confirm data management and/or clinical data management expectations to the business for assigned trial(s) to include but not limited to:
+ Gather and/or review content and integration requirements for Electronic Code of Federal Regulations (eCFR) and other data collection tools.
+ Participate in establishing conventions and quality expectations for clinical data.
+ Participate in establishing expectations for dataset content and structure.
+ Work with others to set timelines and follow-up regularly to monitor delivery of all data management milestones.


* Review clinical data management documents (including submission package) for appropriate quality, scientific content, organization, clarity, accuracy, format, and consistency.

Work with DM...