research-analyst

Australiance is a strategic growth partner specializing in recruitment and internationalization services for innovative startups and SMEs. They offer a wide range of recruitment services to help attract, hire, and retain top talents, both local and international, while providing integrated HR programs and mobility services. Australiance also assists in developing innovation projects by making connections for fundraising and public funding, and offers expertise in expanding internationally, including implementation strategies and networking within a global community. Their joint venture, InAuTalent, combines expertise in internationalization with innovation funding to precisely meet client needs through consulting and recruitment services.

Australiance is a consulting & talent acquisition firm supporting entrepreneurs & professionals to realize their potential in Asia Pacific.With a passion for people and a drive for outstanding connections, Australiance has enabled more than 1000 Startups, SME’s and innovative blue-chip companies to connect with top talents ranging from C-level to young guns. Our business pillars:- Business Consulting: assist international companies with their market entry strategies including local representation, business setup and subsidiary management.- Talent Acquisition: recruit talents, manage the entire hiring employee onboarding and payroll process including payroll, superannuation, tax, etc.- Empower startup community through Startup&Angels: connect promising early stage startups with their next talents, clients and investors.To contact us, please fill in our contact form https://www.australiance.com/contact-us/ Check out our latest job and internship opportunities here: https://australiancetalent.com/job-board/

Australiance

• Conduct research on venture capital funds, managers, and market trends
• Gather and summarise data on fund strategies, performance, and portfolios
• Prepare research notes and comparison materials across funds and managers
• Support internal research across the venture and investment landscape
• Build and maintain Excel-based analysis and comparison models
• Work with quantitative data sets and financial information
• Assist in preparing numerical and research-based internal reports
• Organise and maintain research and due diligence materials
• Assist with collecting and reviewing information from fund managers
• Support internal investment and portfolio reporting
• Contribute to ad-hoc analytical and research tasks as required

Research Analyst Internship

Research Analyst Intern supporting investment research for a growing venture platform. Conducting data analysis and assisting with investment team support in a hybrid working model.

ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.

Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times.

We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.

ICON plc

• Coordinate activities to set up and monitor a study
• Complete accurate study status reports and maintain study documentation
• Submission of protocol, consent documents for ethics/IRB approval
• Assist in preparing regulatory submissions as requested
• Participate in preparing and reviewing study documentation and feasibility studies for new proposals
• Balance sponsor generated queries efficiently and responsible for study cost-effectiveness
• Assist in training and mentoring less expert CRA's and/or lead CRA's working on international projects

Senior Clinical Research Associate

Senior Clinical Research Associate coordinating activities for clinical trials at ICON. Working independently to ensure accurate study documentation and protocol submissions.

Aurora Energy Research is a company based in Oxford that specializes in critical energy market analytics. They provide data-driven intelligence to clients for strategic planning, portfolio management, and investment decisions in the context of the global energy transformation. Their offerings include comprehensive market outlook packages, specialized software tools for assessing wind and battery projects, and bespoke advisory services. Aurora also hosts events and webinars aimed at fostering discussions on vital energy issues while delivering fresh insights through reports and podcasts.

From its academic roots, Aurora Energy Research has grown to become the largest dedicated power market analytics company in Europe, providing data-driven intelligence for strategic decisions in the global energy transformation. We are a diverse team of over 600 experts with vast energy, financial and consulting backgrounds, covering power, hydrogen, carbon and fossil commodities. We are active in Europe, APAC and the US, working with world-leading organisations to provide comprehensive market intelligence, bespoke analytic and advisory services, and cutting-edge software.

Aurora Energy Research

• Lead research reports, from the idea to the presentation to clients and press, under the supervision of the senior leadership in the APAC team
• Keep abreast of developments in policy, markets, and technology, and then use this to develop and provide data-driven insights to clients on how energy markets could develop
• Monitor and provide insights to clients on pathways to procure power in Australia
• Represent the firm at external events as an expert in this rapidly evolving market, and develop our thought leadership, analysis, and subscription product offering
• Play a critical role in product delivery and development, as well as client engagement – identifying client needs, and continuously enhancing the service we provide
• Develop analysis into the energy transition for both public and private sector clients; and present these insights in client meetings and presentations
• Work towards the development of fully integrated Research + Advisory + Software services across the entire company. This means working with other teams and offices in Aurora as well as independently
• You will report to the Research Lead and work within Aurora’s larger Subscription Analytics team


Research Associate – Offtake Product

Research Associate delivering cutting-edge energy analytics and strategic insights in Australia’s energy sector. Engaging with clients and contributing to the global research team’s efforts.

• 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

Senior Clinical Research Associate / Clinical Research Associate II

Experienced Clinical Research Associate at ICON managing clinical trials and collaborating with investigators in Australia. Ensuring compliance and data integrity while contributing to innovative treatments.

Fortrea is a global clinical research organization (CRO) specializing in providing comprehensive clinical development services to biopharma and MedTech companies. With over 30 years of experience, Fortrea offers a range of services including clinical pharmacology, phase I-IV study management, regulatory strategy, market access, and more. They focus on advancing healthcare innovation by integrating data and scientific expertise to deliver tailored solutions that enable faster decision-making and improve patient outcomes, especially in the realm of cell and gene therapy programs, as well as various therapeutic areas like oncology, cardiovascular, and infectious diseases.

Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. 

Our talented and diverse team of approximately 19,000 people working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.

Fortrea

• Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned
• Responsible for all aspects of site management as prescribed in the project plans
• Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study
• Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
• Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review
• Ensure the resources of the Sponsor and Fortrea are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines, including managing travel expenses in an economical fashion according to Fortrea travel policy
• Ensure audit readiness at the site level
• Prepare accurate and timely trip reports
• Participate in and follow-up on Quality Control Visits (QC) when requested
• Track and follow-up on Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs

Clinical Research Associate II

Clinical Research Associate at Fortrea monitoring global clinical trials. Collaborating with stakeholders to ensure patient safety and data integrity while adhering to regulatory guidelines.

IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.

IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. IQVIA Connected Intelligence™ delivers powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 86,000 employees, IQVIA conducts operations in more than 100 countries.

IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific advances, in an effort to advance their path toward cures. To learn more, visit www.iqvia.com.

IQVIA

Join a dynamic team driving cutting-edge clinical trials! As a CRA, you'll be the key link between sponsors and trial sites—ensuring studies run smoothly, data is accurate, and compliance is top-notch. This role is Perth or Brisbane based. Minimum of 18 months monitoring experience is required. Key Responsibilities include leading site visits (selection, initiation, monitoring, close-out), driving subject recruitment and site engagement to meet study goals, delivering protocol training and maintaining strong site communication, monitoring site performance, escalating quality issues, tracking study progress, maintaining Trial Master File (TMF) and Investigator Site File (ISF), documenting findings and collaborating with cross-functional teams to support project execution, and managing site budgets and invoicing.

Clinical Research Associate 2

CRA role overseeing clinical trial execution, ensuring compliance and communication between sponsors and sites. Focused on site performance and data accuracy while based in Brisbane or Perth.

Hybrid Research Analysts roles in Australia

Browse 6 hybrid research analysts roles hiring in Australia plus related opportunities such as data analyst, business analyst, financial analyst, clinical research and analyst.

6 jobs found

Research Analyst Internship

Australiance

Senior Clinical Research Associate

ICON plc

Research Associate – Offtake Product

Aurora Energy Research

Senior Clinical Research Associate / Clinical Research Associate II

ICON plc

Clinical Research Associate II

Fortrea

Clinical Research Associate 2

IQVIA