Senior Clinical Research Associate - Oncology FL State

Added
5 minutes ago
Type
Full time
Salary
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Related skills

gcp monitoring clinical research ich guidelines oncology
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πŸ“‹ Description

  • Considered as the Primary Sponsor point of contact for the investigative site. Advanced level of
  • Aligns, trains and motivates the site staff and principal investigator on the goals of the clinical
  • Conducts site evaluation, site training, routine on-site and off-site monitoring, and site closure
  • Superior understanding of site engagement and ability to customize site engagement strategy for
  • Superior level of competency connecting the study protocol, scientific principles and clinical
  • Possesses advanced level of competency to mentor and train less experienced CRAs on various aspects

🎯 Requirements

  • Appropriate tertiary qualification in health related disciplines (e.g., Medical, Scientific
  • Minimum of 3 years of clinically related experience, of which a period of 2 years is preferable in
  • Knowledge of appropriate therapeutic area indications with the ability to understand and apply
  • Superior knowledge on existing and emerging local regulatory and legal requirements, ICH/GCP
  • Demonstrate advanced communication skills and superior cross-functional collaboration skills among
  • Demonstrate superior planning and organizational skills and the ability to work effectively and

🎁 Benefits

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