Work History

Solutions Engineer

  • Organisation: OpenClinica LLC
  • Department: Product and Service Development / Customer Support
  • Reporting to: OpenClinica CEO
  • Duration: 2017-08 to present (11 months)

Responsibilities

  • Develop a new, enhanced ETL and self-serve capable reporting and analytics solution
  • Potential customer demonstrations of the reporting module
  • Technical support

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 and vendor management for SRI data systems, including the Clinical Trials portal and Grants Management System
  • Identify and oversee or implement system enhancements, changes or upgrades to SRI data systems
  • Implement tools and processes for reporting to meet diverse stakeholder requirements, leveraging appropriate tools such as SQL, PowerShell, R, Qlik

Solutions Engineer

  • Organisation: OpenClinica LLC
  • Department: Product and Service Development / Customer Support
  • Reporting to: OpenClinica CEO
  • Duration: 2017-01 to 2017-03 (3 months)

Responsibilities

  • Prototype a new, enhanced ETL and self-serve capable reporting and analytics solution

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

  • System support for VHCRP data systems, including OpenClinica and mobile data collection
  • Implement data collection and validation systems for projects from the VHCRP
  • Implement tools and processes for reporting, mobile device preparation and management

Achievements

  • Implemented OpenClinica systems for:
    • NCT02102451 (CEASE): surveillance of hepatitis C treatment
    • NCT02064049 (SToP-C): phase 4 hepatitis C
    • Healthy Liver Campaign (LiverLife): Liver health promotion among injecting drug users
    • NCT01364090 (ACTIVATE): phase 4 hepatitis C
    • NCT01336010 (ATAHC II): phase 4 hepatitis C
    • NCT01743521 (DARE-C): phase 4 hepatitis C
    • NCT02156570 (DARE-C II): phase 4 hepatitis C
  • Implemented ODK Collect systems for:
    • LiverLife (as above)
    • SToP-C (as above)
    • NCT02336139 (SIMPLIFY): phase 2 hepatitis C
  • Implemented a LimeSurvey survey for CEASE (as above)

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 data collection and validation systems for CTC projects
  • Train project staff in data management with OpenClinica and TeleForm
  • User management and system support

Achievements

  • Implemented OpenClinica systems for:
    • ACTRN12611000378921 (SEED): quality of life study for brain cancer
    • ACTRN12610000796088 (PARAGON): phase 2, gynaecological cancer
  • Implemented TeleForm Optical Character Recognition systems for:
    • ACTRN12610000796088 (PARAGON): phase 2, gynaecological cancer
    • ACTRN12605000055606 (BOOST II): phase 3, neonatal health

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

  • Study start-up phase: conduct feasibility surveys, vendor selection, write study documentation, ethics and regulatory applications, data systems specifications;
  • Study conduct phase: collect, distribute and track GCP Essential Documents; data collection, entry, and validation; safety and project progress reporting; coordinate pathology sample collection;
  • Study closure phase: finalise GCP Essential Documents, data cleaning, and distribute final reports;

Achievements

  • Worked on:
    • ACTRN12611000245998 (TACTIC): phase 2, biliary tract cancer
    • ACTRN12609000158268 (LAP07): phase 3, pancreatic cancer
    • ACTRN12609000109202 (ATTAX3): phase 2, oesophago-gastric cancer
    • ACTRN12605000361606 (ESPAC-3): phase 3, pancreatic cancer
    • ACTRN12608000382370 (DECO): phase 2 oesophageal cancer
  • 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

  • Obtain, file and track GCP Essential Documents
  • Quality of Life questionnaire data entry
  • Assist the study coordination team

Achievements

  • Worked on:
    • ACTRN12605000025639 (MAX): phase 2/3, colorectal cancer
    • ACTRN12605000359639 (DaVINCI): phase 2, colorectal cancer
    • ACTRN12607000294459 (Accelerated BEP): phase 1/2, germ cell cancer
    • ACTRN12608000254392 (Aprepitant): phase 2, germ cell cancer
    • ACTRN12609000545268 (Chemo and Cog): quality of life study for testicular cancer