Lead Clinical Data Analyst

Johnson & Johnson MedTech

Leeds, West Yorkshire, United Kingdom
Not specified (assumed hybrid due to industry standard)
Clinical system support and management
Project management for clinical studies
Experience with medidata or veeva systems
Johnson & Johnson MedTech is seeking a Lead Clinical Data Analyst for their DePuy Synthes team in Leeds, UK. The role involves overseeing clinical study databases and requires strong project management skills, experience with clinical systems, and collaboration across various teams

Job Summary

  • Johnson & Johnson is committed to building innovative healthcare solutions that profoundly impact health for humanity.
  • The Lead Clinical Data Analyst will coordinate timelines and resources to implement and maintain clinical systems and manage clinical study databases across various platforms.
  • The role involves collaboration across multiple departments and vendors, supporting global harmonized processes, and mentoring peers to ensure quality deliverables.

Matching Summary

Match Score: 85

Johnson & Johnson MedTech is seeking a Lead Clinical Data Analyst for their DePuy Synthes team in Leeds, UK. The role involves overseeing clinical study databases and requires strong project management skills, experience with clinical systems, and collaboration across various teams.

Skills & Requirements

Must-have

  • Clinical system support and management
  • Project management for clinical studies
  • Experience with Medidata or Veeva systems
  • Coordination of clinical study databases
  • Vendor evaluation and oversight
  • Collaboration with cross-functional teams

Nice-to-have

  • Advanced certification in clinical systems
  • Knowledge of CDISC STDM standards
  • Experience in Clinical Operations
  • Strong verbal and written communication
  • Training and mentoring peers
  • Understanding of GCP and SDLC

Key Requirements

  • Bachelor’s degree in Statistics, Computer Science or related discipline
  • At least 6 years system support experience in clinical research
  • Experience with EDC, CTMS, eTMF, and IxRS clinical systems
  • Proven experience with Medidata or Veeva systems
  • Travel up to 10% allowed

Work Rights

Not specified

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