Clinical Research Associate II

Added
1 hour ago
Type
Full time
Salary
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Related skills

gcp clinical research ich guidelines site management regulatory compliance
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📋 Description

  • Considered as the primary point of contact for the investigative site.
  • Aligns, trains and motivates the site staff and principal investigator on the goals of the clinical
  • Conducts site evaluation, site training, routine, and site closure monitoring activities with
  • Advanced understanding of site engagement and ability to customize site engagement strategy for
  • Gather local/site insights and utilize site engagement tools such as the Customer Relationship
  • Advanced level of competency connecting the study protocol, scientific principles and clinical

🎯 Requirements

  • Bachelor's Degree in health related disciplines (Medical, Scientific, Nursing) preferred.
  • Previous experience as CRA is required (performing investigation monitoring and similar functions).
  • Minimum of 1 year of clinically related experience, of which a period of 6 months is required in
  • Familiar with risk‐based monitoring approach, onsite and off site monitoring.
  • Knowledge of appropriate therapeutic area indications is preferred with the ability to understand
  • Advanced knowledge on existing and emerging local regulatory and legal requirements, ICH/GCP

🎁 Benefits

  • Comprehensive package of benefits including paid time off (vacation, holidays, sick)
  • This job is eligible to participate in short-term incentive programs.
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