Remote Clinical Research Associate II – Australia

KCR Placement

Sydney

Remote

AUD 90.000 - 120.000

Vollzeit

Vor 5 Tagen
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

Annual leave entitlements
Health insurance offerings
Retirement planning offerings
Global Employee Assistance Programme

Zusammenfassung

ICON is seeking a Clinical Research Associate II based in Australia, with home-based flexibility. The role involves monitoring clinical trials, ensuring protocol adherence, data integrity, and patient safety, while collaborating with investigators and site staff to support study conduct.

Ideal candidates have a science/healthcare degree and at least 2 years of independent CRA monitoring experience, along with strong organizational and communication skills and the ability to travel as needed.

Qualifikationen

  • Bachelor's degree in a scientific or healthcare-related field.
  • Minimum of 2 years of independent monitoring experience as a Clinical Research Associate within CRO/Pharma.
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.

Aufgaben

  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
  • Collaborating with investigators and site staff to facilitate smooth study conduct.
  • Performing data review and resolution of queries to maintain high-quality clinical data.
  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports.

Kenntnisse

Organizational skills
Communication skills
Independent work
Team collaboration
Travel willingness

Ausbildung

Bachelor's degree in science/healthcare

Jobbeschreibung

ICON is seeking a Clinical Research Associate II based in Australia, with home-based flexibility. The role involves monitoring clinical trials, ensuring protocol adherence, data integrity, and patient safety, while collaborating with investigators and site staff to support study conduct.

Ideal candidates have a science/healthcare degree and at least 2 years of independent CRA monitoring experience, along with strong organizational and communication skills and the ability to travel as needed.

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