Title: Chair Human Research Ethics Committee Location: Gold Coast Australia Job Description: Job details Position status Fixed Term Temporary Position type Part-time Occupational group Research Classification HSO Workplace Location Gold Coast Job ad reference QLD/GC684926 Yearly salary Fortnightly salary Total remuneration Salary Other Job duration 12 months (with the possibility of extension)  Access the National Relay Service The Role An opportunity has become available for a Chair Human Research Ethics Committee to join Gold Coast Health (GCH) where the focus of our 13 000-strong team is on providing world-class health care to people living in the Gold Coast, and northern New South Wales region of Australia. You will - Provide leadership to the Gold Coast Health Human Research Ethics Committee (HREC) on matters concerning research ethics and research review within meetings - Ensure that the HREC functions in accordance with the requirements as set out in the National Statement and in accordance with The Australian Code for the Responsible Conduct of Research (2018) - Chair monthly HREC meetings in an efficient, expeditious and fair manner ensuring that ethical aspects of the research studies submitted are discussed at the meetings - Lead and take responsibility for the provision of ethical decision making in respect of research involving human subjects for all research applications About you To be successful in this position you will require: - Evidence of vaccination, or be able to be vaccinated against and remain vaccinated against - Measles, Mumps, Rubella, Varicella, Pertussis and Hepatitis B - Tuberculosis screening, to identify if the tuberculosis vaccination may be required - Paid Blue Card (Working with Children Check) - Declaration of serious discipline history must be disclosed - Criminal History Screening will be required for new employees (GCH will cover cost) Benefits - Flexible work options - Career Development - Salary Packaging - Modern Facilities - Diverse Work Culture - Research Opportunities - 12.75% super - 17.5% leave loading Salary - Temporary part time (12 months with the possibility of extension) - Base salary ranging from $87.93 - $94.85 per hour About Gold Coast Health - Nationally and internationally recognised location for innovative medical research and health care - Annual operating budget exceeding $1.5 billion - More than 1100 beds across three hospitals - Gold Coast University Hospital, Robina Hospital, Varsity Lakes Hospital and Robina and Southport Health Precincts - Secondary and tertiary health services across more than 20 facilities - Opportunity to combine professional advancement, job satisfaction and relaxation into one fulfilling lifestyle - A workplace culture that encourages people to bring their whole selves to work so that they can perform at their best - Committed to reflecting the diversity of the Gold Coast community and ensuring each staff member is included and feels like they belong

Role Description We're looking for a Property Research Analyst (PRA) to join our fast-growing team. This is a full-time, offshore position that plays a critical behind-the-scenes role in enabling our sales team by qualifying leads and evaluating property suitability for Backyard installations. This is not a customer-facing role. Instead, you’ll serve as a research and operations partner to our Sales Team, helping them focus on what they do best, building client relationships and closing deals. What You’ll Do - Evaluate Properties - Analyze properties across California for ADU feasibility based on delivery feasibility, zoning, lot size, setbacks, and local permitting requirements. - Use GIS tools, property data platforms, and internal checklists to determine site compatibility. - Collaborate with Project Specialists to prioritize high-potential opportunities. - Support Lead Qualification - Review and validate inbound leads for completeness and basic eligibility. - Research ownership records, permitting history, and other relevant data to support Project Specialist decision-making. - Organize and maintain accurate lead information in our CRM system (Salesforce). - Streamline Sales Operations - Tag and categorize leads to improve pipeline visibility. - Flag duplicate or unqualified entries to maintain CRM hygiene. - Help build a system of scalable, repeatable qualification workflows. - Collaborate with Sales Team - Serve as the first point of analysis before a lead is passed to a Project Specialist. - Communicate findings clearly and concisely to the Sales Team. - Participate in occasional alignment meetings with Project Specialists to continuously improve qualification processes. Qualifications - Highly organized with great attention to detail. - Analytical thinker who enjoys solving operational challenges. - Tech-savvy, with comfort navigating CRMs, spreadsheets, and online research tools. - Proactive and able to manage your own workload with minimal supervision. - Strong written and spoken English skills to clearly document findings and communicate with internal stakeholders. - Experience in real estate, proptech, urban planning, GIS, or construction is a plus, but not required. Benefits - This is a unique opportunity to be part of a mission-driven company building beautiful, functional housing solutions. - As an early member of our global research team, you’ll help define the operational backbone of our Sales function. - You’ll work with a team that values curiosity, collaboration, and continuous learning - all while making a real impact in the housing space. Job Details - Position: Full-time - Location: Remote, Offshore - Time Zone Coverage: Must be available for some overlap with US Pacific Time hours

• Analyze properties across California for ADU feasibility based on delivery feasibility, zoning, lot size, setbacks, and local permitting requirements. • Use GIS tools, property data platforms, and internal checklists to determine site compatibility. • Collaborate with Project Specialists to prioritize high-potential opportunities. • Review and validate inbound leads for completeness and basic eligibility. • Research ownership records, permitting history, and other relevant data to support Project Specialist decision-making. • Organize and maintain accurate lead information in our CRM system (Salesforce). • Tag and categorize leads to improve pipeline visibility. • Flag duplicate or unqualified entries to maintain CRM hygiene. • Help build a system of scalable, repeatable qualification workflows. • Serve as the first point of analysis before a lead is passed to a Project Specialist. • Communicate findings clearly and concisely to the Sales Team. • Participate in occasional alignment meetings with Project Specialists to continuously improve qualification processes.

• Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance • Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicates/escalates serious issues to the project team and develops action plans • Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes • Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate • Demonstrates diligence in protecting the confidentiality of each subject/patient • Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues • Assesses site processes as per the Clinical Monitoring/Site Management Plan (CMP/SMP) • Conducts Source Document Review of appropriate site source documents and medical records • Verifies required clinical data entered in the case report form (CRF) is accurate and complete • Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines • Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture • Verifies site compliance with electronic data capture requirements • May perform investigational product (IP) inventory, reconciliation and reviews storage and security • Verifies the IP has been dispensed and administered to subjects/patients according to the protocol • Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations • Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan • Supports subject/patient recruitment, retention and awareness strategies • For assigned activities, understands project scope, budgets, and timelines; manages site-level activities / communication to ensure project objectives, deliverables and timelines are met