Work History

Principal Consultant

  • Organisation: Lindsay Stevens Pty Ltd
  • Department: Consultant
  • Reporting to: Self
  • Duration: 2017-01 to present (3 years, 6 months)

Responsibilities

  • Analyse and fulfil client requirements in the clinical research data space.
  • Design and implement software, reports, and analysis.

Systems Analyst / Architect

  • Organisation: Cancer Institute NSW, NSW Health
  • Department: Strategic Research and Investment (SRI) Division, Data Intelligence Team
  • Reporting to: Data Intelligence Manager
  • Duration: 2017-03 to 2017-08 (5 months)

Responsibilities

  • System support, vendor management, and project management for SRI data systems.
  • Implement tools and processes for reporting to meet stakeholder requirements.

Achievements

  • Implemented grants report reflecting complex business rules in the SRI Clinical Trials portal.
  • Established reproducible reporting system and processes for grants tracking system.

Clinical Trials Database Developer

  • Organisation: UNSW Australia
  • Department: Kirby Institute, Viral Hepatitis C Research Program (VHCRP)
  • Reporting To: VHCRP Clinical Trials Manager
  • Duration: 2013-06 to 2016-12 (3 years 6 months)

Responsibilities

  • Implement and support data management systems for clinical research projects.
  • Implement and support tools and processes for data integration, reporting, mobile device management.

Achievements

  • Implemented OpenClinica data collection systems for 7 phase 4+ hepatitis C studies
  • Implemented ODK Collect mobile PRO data systems for 3 phase 3+ hepatitis C studies
  • Implemented LimeSurvey web PRO data systems for 1 phase 4+ hepatitis C study

Clinical Data Coordinator

  • Organisation: University of Sydney
  • Department: NHMRC Clinical Trials Centre (CTC), Data Management
  • Reporting To: Head of Data Management
  • Duration: 2012-05 to 2013-06 (1 year 1 month)

Responsibilities

  • Implement and support data management systems for clinical research projects.
  • Implement and support tools and processes for data integration and reporting.

Achievements

  • Implemented OpenClinica systems 2 oncology phase 2+ studies.
  • Implemented TeleForm OCR systems for 2 phase 2+ oncology/neonatal studies.

Trial Coordinator / Data Manager

  • Organisation: University of Sydney
  • Department: NHMRC Clinical Trials Centre (CTC), Oncology Trials Program
  • Reporting To: Associate Oncology Program Manager
  • Duration: 2010-07 to 2012-05 (1 year 10 months)

Responsibilities

  • Clinical research project management in accordance with GCP
  • Data management, monitoring, and internal or regulatory reporting
  • Familiarity with start-up, conduct and close-out phases of large, multi-centre projects

Achievements

  • Coordinated or managed (as part of a team) 5 phase 2+ oncology studies
  • Prepared specifications for a clinical trials management system for the centre

Clinical Trials Assistant / Data Manager

  • Organisation: University of Sydney
  • Department: NHMRC Clinical Trials Centre, Oncology Trials Program
  • Reporting To: Associate Oncology Program Manager
  • Duration: 2008-07 to 2010-07 (2 years)

Responsibilities

  • Assist the research project team with project and data management.
  • Data entry, filing, preparation of study binders or other materials.

Achievements

  • Contributed to the coordination or management of 5 phase 2+ oncology studies