Clinical Trial Data Entry & Compliance Officer

University of Sydney

Sydney

Vor Ort

AUD 73.000 - 103.000

Teilzeit

Vor 5 Tagen
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

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Zusammenfassung

The University of Sydney is offering a casual opportunity in the School of Health Sciences Administration to support clinical trials. The role focuses on data capture, data entry, and adherence to GCP and SOPs, with an emphasis on quality outcomes.

You will work under supervision, coordinating trial activities, engaging with stakeholders, and ensuring safety and regulatory compliance while developing professional skills in a supportive academic environment.

Qualifikationen

  • Currently studying or completed a qualification in Health Sciences or related discipline.
  • Knowledge of COPD or related conditions is preferred.
  • Ability to work with others and manage competing priorities to meet deadlines.
  • Excellent verbal and written communication, with quality customer service.
  • High computer literacy and experience with data entry and record management.
  • Strong organisational and time management skills.

Aufgaben

  • Coordinate and assist in various clinical trial activities under supervision.
  • Lead data capture and entry to ensure accuracy and compliance with GCP/SOPs.
  • Review ethics guidelines, WHS requirements and trial standards.
  • Develop relationships with clinical trial stakeholders and facilitate communication.
  • Prioritise health and safety and participate in safety drills and training.

Kenntnisse

Health sciences
COPD knowledge
Communication skills
Data entry
Time management
Team collaboration
Computer literacy

Ausbildung

Health Sciences / related discipline

Jobbeschreibung

The University of Sydney is offering a casual opportunity in the School of Health Sciences Administration to support clinical trials. The role focuses on data capture, data entry, and adherence to GCP and SOPs, with an emphasis on quality outcomes.

You will work under supervision, coordinating trial activities, engaging with stakeholders, and ensuring safety and regulatory compliance while developing professional skills in a supportive academic environment.

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