Lead Clinical Data Analyst

Johnson & Johnson

Leeds, West Yorkshire, United Kingdom
Base: $109,000.00 - $174,800.00; bonus/equity: not...
Clinical system support and management
Project management for clinical trials
Experience with medidata or veeva systems
The Lead Clinical Data Analyst will coordinate timelines and resources required to implement and maintain a variety of clinical systems as well as provide oversight and coordination of all aspects of the development and management of clinical study databases across a variety of platforms

Job Summary

  • The Lead Clinical Data Analyst will coordinate timelines and resources required to implement and maintain a variety of clinical systems as well as provide oversight and coordination of all aspects of the development and management of clinical study databases across a variety of platforms.
  • Johnson & Johnson is committed to providing an inclusive work environment where each person is considered as an individual and respects the diversity and dignity of its employees.
  • The role involves collaboration across multiple teams including Data Management leadership, Clinical Operations, IT, and Quality to deliver clinical system solutions that support innovative orthopedic treatments.

Matching Summary

The Lead Clinical Data Analyst will coordinate timelines and resources required to implement and maintain a variety of clinical systems as well as provide oversight and coordination of all aspects of the development and management of clinical study databases across a variety of platforms.

Salary

Base: $109,000.00 - $174,800.00; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Clinical system support and management
  • Project management for clinical trials
  • Experience with Medidata or Veeva systems
  • Coordination of clinical study databases
  • Vendor evaluation and oversight
  • Collaboration with Clinical Operations and Biostatistics

Nice-to-have

  • Advanced certification in clinical systems
  • Knowledge of CDISC STDM standards
  • Experience with Clinical Operations
  • Strong verbal and written communication
  • Knowledge of GCP and SDLC
  • Mentoring and training development

Key Requirements

  • Bachelor’s degree in Statistics, Computer Science or related discipline
  • At least 6 years clinical research system support experience
  • Experience with EDC, CTMS, eTMF, and IxRS clinical systems
  • Proven project management experience
  • Travel up to 10%
  • Preferred knowledge of GCP and SDLC
  • Preferred experience with CDISC STDM

Work Rights

Not specified

Tailored Resume

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