Clinical Research Associate II

Added
22 days ago
Type
Full time
Salary
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Related skills

gcp cross-functional collaboration clinical research site monitoring ich guidelines
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📋 Description

  • Considered as the primary point of contact for the investigative site. High level of competency or
  • 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
  • Advanced level of competency connecting the study protocol, scientific principles and clinical
  • Develop solid knowledge of therapeutic area, asset and clinical landscape / patient journey to

🎯 Requirements

  • Bachelor's Degree in health related disciplines (Medical, Scientific, Nursing) preferred.
  • 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
  • Demonstrate strong cross-functional collaboration skills among internal and external stakeholders.

🎁 Benefits

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