Clinical Research Associate

Added
6 days ago
Type
Full time
Salary
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Related skills

gcp monitoring clinical research ich guidelines site management
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📋 Description

  • Acts as primary Sponsor point of contact for investigative sites, providing contextual information
  • Aligns, trains, and motivates site staff and principal investigators on clinical trial goals
  • Conducts site evaluation, training, routine on-site/off-site monitoring, and closure activities in
  • Customizes site engagement strategies, gathers local insights, and tracks/reports progress and
  • Ensures effective patient recruitment and retention plans based on disease journey; develops
  • Mentors and trains less experienced CRAs; supports onboarding of junior CRAs.

🎯 Requirements

  • Bachelor's degree or equivalent; health-related field (Medical, Scientific, Nursing, Pharmacy)
  • Minimum of 3 years clinically related experience; for Sr.CRA, 2 years in independent clinical
  • Knowledge of appropriate therapeutic area indications and ability to apply scientific concepts.
  • Knowledge of local regulatory/legal requirements, ICH/GCP Guidelines, and applicable policies.
  • Advanced communication, cross-functional collaboration, planning, and organizational skills.
  • Ability to leverage technology and tools for customer-centric support.
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