Global Data Manager

Johnson & Johnson-posted 11 months ago
Full-time • Entry Level
Titusville, FL
5,001-10,000 employees
Chemical Manufacturing
Resume
Match Score
Upload and Match ResumeTrack Jobs with Teal

Johnson & Johnson is currently seeking a Global Data Manager. This position can be located in Spring House, PA; Titusville, NJ; or Raritan, NJ. 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). Work is received in broad terms and reviewed on an ongoing basis with DML and the amount of instruction is limited.

  • Take on a leadership role 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).
  • Gather and/or review content and integration requirements for Electronic Code of Federal Regulations (eCFR) and other data collection tools.
  • Establish conventions and quality expectations for clinical data.
  • Establish expectations for dataset content and structure.
  • 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.
  • Ensure compliance with regulatory guidelines and the documentation matrix.
  • Ensure real-time inspection readiness of all DM deliverables for the trial and participate in regulatory agency and Johnson & Johnson internal audits as necessary.
  • Plan and track content, format, quality, and timing of applicable data management deliverables.
  • Create key functional plans (e.g. study Integrated Review Plan) ensuring appropriate quality, scientific content, organization, clarity, accuracy, format, and consistency.
  • Identify and communicate lessons learned, best practices, and frequently asked questions at the trial level.
  • Identify and participate in process, system, and tool improvement initiatives.
  • Perform trial level oversight controls and/or execute data management activities per applicable procedures, with DML direction.
  • Bachelor's degree in a relevant field.
  • Strong analytical skills and attention to detail.
  • Ability to work collaboratively in a team environment.
  • Excellent communication skills, both written and verbal.
  • Familiarity with data management processes and regulatory guidelines.
  • Experience in clinical data management or related field.
  • Knowledge of Electronic Code of Federal Regulations (eCFR).
  • Previous experience working with external suppliers and trial customers.
  • Comprehensive health insurance.
  • 401(k) retirement plan with company matching.
  • Paid time off and holidays.
  • Opportunities for professional development and career advancement.
  • Diversity, equity, and inclusion programs.
Track Jobs with Teal

Job Search Resources

•
AI Resume Builder
•
Global Project Manager Resume Examples
•
Global Project Manager Cover Letter Examples

Tools

Career Hubs

Guides

Company

© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service