Clinical Research Associate - Medical Imaging - SaMD - AU
Job details
Why join us? Do work that matters. We’re pioneering AI software that will help diagnose medical images and raise the standard of healthcare for millions of people every day. Well-funded and global. annalise.ai has a global presence across APAC, EU and US regions. We’re backed by I-MED radiology and harrison.ai (raised Australia’s largest Series B of $129m in 2021). Work with a bunch of awesome, genuine people who are passionate about what they do. Flexible and remote-friendly working Make an impact . You won’t be another ‘cog in the wheel’ here. We give full trust and autonomy for you to be heard, to work on big & complex projects – and to make a real difference. Grow your career with us. We’re big believers in lifelong learning. You’ll be given a $1000 personal L&D budget, access to LinkedIn Learning, plus opportunities for internal mobility and leadership training to fast-track your career. Generous parental support including 16 weeks gender-neutral paid parental leave and $10,000 support for egg or sperm freezing. Do your best work and have fun doing it with unlimited well-being leave, monthly meditations, inclusive team events, and lots more! As a Clinical Research Associate, at Annalise.ai , you will play a vital role supporting the clinical evaluation of software as medical device (SaMD) artificial intelligence (AI) products used in diagnostic medical imaging. This role is an exciting opportunity for a highly motivated, experienced Clinical Research Associate to join a uniquely talented Clinical Research and Medical Affairs team, who’s primary department focus is to conduct clinical studies in accordance with applicable standards and regulations, and generate high quality clinical documentation supporting the regulatory and marketing strategy for Annalise.ai products. Reporting to the Clinical Operations Manager, you will be responsible for the planning and generation of a wide range of documentation supporting the evaluation of Annalise.ai SAMD, including state of the art reviews, clinical evaluation plans and reports, and other post-market documentation to support regulatory submissions. You will also have opportunity to contribute to the dissemination and publication of clinical evidence for Annalise.ai devices. This role will see you coordinate interactions between a range of internal and/or external stakeholders and Subject Matter Experts (SMEs), so you will need strong written and verbal communication skills. You will have experience writing clinical documents in accordance with applicable standards and regulations within a medical device setting. As we pioneer new ways of improving health delivery at scale using the most cutting-edge AI technologies, we invite you to consider an exciting, meaningful role with the Clinical Research and Medical Affairs team here at Annalise.ai . What you'll do:
- Develop and maintain scientific knowledge in the state of the art for AI-based radiology SaMD by conducting systematic literature reviews.
- Establishing clinical evidence database for Annalise.ai products and identifying the competitor landscape.
- Assist with the development and maintenance of clinical evaluation plans and reports, and other relevant post-market documentation supporting the regulatory submissions for SaMD.
- Contribute to the evidence dissemination strategy by preparing conference abstracts and/or high-quality manuscripts for peer-reviewed publication.
- Effectively manage liaisons between internal and external stakeholders from cross-functional teams.
- Perform quality assurance and manage document reviews, ensuring all documents are well organized, scientifically accurate, consistent, and in compliance with applicable Standard Operating Procedures (SOPs), guidelines and regulations.
- Contribute to the development or updating of relevant SOPs in line with relevant guidelines and regulations.
- Complete documents within a period that supports the product roadmap and deadlines.
- Bachelor’s degree in a scientific or related field (e.g., medical sciences, pharmacology, engineering).
- 1-3 years of experience in clinical research, medical affairs or a related function within the pharmaceutical, biotechnology, or medical device industry.
- Proficiency in conducting systematic and efficient literature searches to identify relevant scientific and technical literature.
- Ability to comprehend, critique, analyse and synthesise large amounts of scientific and clinical data.
- Excellent oral communication and technical writing skills.
- Able to work independently as well as collaborate within a larger team.
- Strong interpersonal skills and experience managing stakeholders from cross-functional teams.
- Detail-oriented, organised with the ability to manage multiple projects simultaneously.
- Masters/PhD or post-graduate qualification in a relevant area of medical science.
- Experience working in research involving artificial intelligence, SaMD, radiology or related medical imaging field.
- Knowledge of Good Clinical Practice or other harmonised standards.
- Familiarity with clinical evaluation processes and other regulatory compliance requirements in major markets (EU, US and Australian Medical Device Regulations).
- Established publication record.
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