Senior Clinical Research Asssociate

Added
8 days ago
Type
Full time
Salary
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Related skills

gcp monitoring data integrity clinical research ich

๐Ÿ“‹ Description

  • Advance AbbVie\'s pipeline by striving for excellence in clinical research and partner with study
  • Focus on site clinical research to ensure proper trial conduct, data integrity, and study
  • Lead and mentor monitoring teams; align site staff and investigators with trial goals and patient
  • Conduct site evaluations, training, monitoring activities, and site closure with adherence to
  • Develop and optimize site engagement strategies and recruitment/retention plans based on patient

๐ŸŽฏ Requirements

  • Appropriate tertiary qualification in health-related disciplines preferred.
  • Minimum 3 years of clinically related experience, with 2 years in independent clinical research
  • Knowledge of regulatory requirements (ICH/GCP) and risk-based monitoring; strong communication and
  • Excellent planning, organizational, and stakeholder engagement abilities; ability to work in
  • Advanced ability to leverage technology/tools to provide site-centric support.
  • Ability to mentor junior CRAs and contribute to onboarding and training.

๐ŸŽ Benefits

  • Professional development
  • Paid time off, wellness programs, retirement savings
  • Competitive compensation
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