Clinical Research Associate II

Added
5 hours ago
Type
Full time
Salary
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Related skills

gcp clinical trials clinical research site monitoring ich guidelines

📋 Description

  • Act as the primary Sponsor point of contact for the investigative site, providing contextual
  • Aligns, trains and motivates the site staff and principal investigator on the goals of the clinical
  • Conduct site evaluation, site training, routine on-site and off-site monitoring, and site closure
  • Advanced understanding of site engagement and ability to customise site engagement strategy for
  • Gather local/site insights and utilise site engagement tools to report/track progress and measure
  • Connect the study protocol, scientific principles and clinical trial requirements to the day-to-day

🎯 Requirements

  • Bachelor's degree or equivalent degree; health related preferred (e.g. Medical, Scientific
  • Minimum of 1 year of clinically related experience, of which a period of 6 months is required in
  • Experience in Healthy Volunteer and First in Patient trials highly desirable
  • Familiarity with risk‐based monitoring approach, onsite and offsite monitoring.
  • Demonstrate strong cross-functional collaboration skills among internal and external stakeholders.
  • Demonstrate strong planning and organisational skills and the ability to work effectively and

🎁 Benefits

  • Flexibility and Availability: In line with Australia's 'Right to Disconnect' legislation, we
  • Equal opportunity employer, dedicated to fostering an inclusive, flexible, and supportive workplace.
  • Commitment to operating with integrity, driving innovation, transforming lives, and embracing
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