Clinical Research Associate II - Dermatology (Southern California)

Added
8 hours ago
Type
Full time
Salary
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Related skills

gcp clinical research site monitoring ich guidelines sop
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πŸ“‹ Description

  • Partners with the investigator and site staff for meaningful and effective engagements positioning
  • Considered as the primary point of contact for the investigative site.
  • Provides contextual information on clinical trials, connects stakeholders to investigative sites
  • Aligns, trains, and motivates site staff and principal investigator on the goals of the clinical
  • Conducts site evaluation, site training, routine, and site closure monitoring activities with
  • Demonstrates advanced understanding of site engagement and customizes site engagement strategy for

🎯 Requirements

  • Appropriate tertiary qualification in health related disciplines (Medical, Scientific, Nursing)
  • Minimum of 1 year of clinically related experience, with 6 months in clinical research monitoring
  • Familiar with risk-based monitoring approach, onsite and offsite monitoring.
  • Knowledge of appropriate therapeutic area indications preferred with ability to understand and
  • Advanced knowledge of existing and emerging local regulatory and legal requirements, ICH/GCP
  • Strong cross-functional collaboration skills among internal and external stakeholders.

🎁 Benefits

  • Paid time off (vacation, holidays, sick)
  • Medical, dental, and vision insurance
  • 401(k)
  • Eligibility for short-term incentive programs
  • Potential for other compensation and benefits as per company discretion
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