Senior Clinical Research Asssociate

Added
6 days ago
Type
Full time
Salary
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Related skills

gcp clinical research site monitoring ich site management
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๐Ÿ“‹ Description

  • Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into
  • Partner with study teams, AbbVie R&D stakeholders, investigators, and site staff for
  • Focus on site clinical research to ensure proper conduct, data integrity, and study performance.

๐ŸŽฏ Requirements

  • Appropriate tertiary qualification in health disciplines preferred.
  • Minimum 3 years clinically related experience; 2 years in independent clinical research monitoring.
  • Knowledge of regulatory requirements, ICH/GCP guidelines, and applicable policies.
  • Strong communication and cross-functional collaboration skills.
  • Excellent planning, organization, and ability to manage multiple projects.
  • Proficiency with technology and tools to support site-centric service delivery.

๐ŸŽ Benefits

  • Competitive compensation package.
  • Great place to work with professional development opportunities.
  • Paid time off, wellness programs, and retirement savings options.
  • Flexible health insurance and employee stock purchase plan.
  • Bonus plan and work-life balance initiatives.
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