At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions 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
Job Function: Data Analytics & Computational Sciences
Job Sub Function: Clinical Data Management
Job Category: People Leader
All Job Posting Locations: High Wycombe, Buckinghamshire, United Kingdom
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Data Analysis Standards Director
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at
We are searching for the best talent for a Data Analysis Standards Director in our Clinical Data Standards (CDS) team to guide and support direct reports in the delivery of the CDS goals and objectives, providing meaningful input for their career development. As a member of the CDS leadership team, the position provides expertise and input for the development of the CDS strategy and oversight. The position may be located: High Wycombe, United Kingdom; Breda, Netherlands; Beerse, Belgium; Allschwil, Switzerland, or Raritan/Spring House/Titusville, United States. Hybrid preferred (3 days onsite weekly). Remote options will be considered on a case by case basis and with approval from the company.
The Data Analysis Standards Director is responsible for overseeing the definition and execution of the CDS vision and strategy to enable J&J clinical trials with fit-for-purpose standards primarily focusing on analysis standards for use in clinical trials, including but not limited to assessments and statistical endpoints, statistical methods, ADaM metadata, and displays used in the clinical report. The position is responsible for ensuring that standards are structured and governed in a manner that is well-aligned with stakeholder processes in order to maximize efficiencies and value. The position is responsible for operational fit and ensuring that these standards have incorporated the best available medical knowledge and comply with relevant regulatory requirements and industry standards. The position operates in a matrix environment, collaborating with cross functional leaders in IDAR (Integrated Data Analytics & Reporting), GD (Global Development) and other functions.
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