Clinical Associate, Digital Health
Clinical Associate, Digital Health
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Job Description
About the role:
The Clinical Associate Digital Health role supports the execution of cutting-edge digital health research projects in collaboration with healthcare partners investigators and internal teams. This role is ideal for someone with a clinical background such as nursing allied health or clinical operations who is looking to pivot into research and innovation. Youll contribute to study documentation participant monitoring and compliance helping generate high-quality evidence for digital health technologies.
Please note this is a Queensland based role
About you:
You may have started your career in a clinical setting and are now ready to apply your hands-on experience to research and development. Youre detail-oriented organised and thrive in collaborative environments. Youre eager to learn more about digital health clinical research standards and regulatory frameworks and you bring a strong understanding of clinical workflows and patient care
Key responsibilities:
Execute and monitor digital health research studies: Ensure compliance with GCP ethics and regulatory standards while supporting pilot and feasibility studies.
Coordinate cross-functional collaboration: Work with internal teams (Compliance Legal Clinical Research) and external partners to align project goals and timelines.
Maintain accurate study documentation: Manage protocols consent forms training logs and regulatory files ensuring secure storage and data integrity.
Support operational logistics: Assist with investigator meetings training sessions cadaver lab procedures and live subject monitoring.
Contribute to data and technical translation: Perform data entry and reporting and help translate clinical workflows into technical requirements for R&D teams.
Must have experience/skills:
Bachelors degree in Life Sciences Nursing Biomedical Engineering or equivalent experience;
Minimum 2 years in clinical research clinical operations or healthcare/medical device R&D with 4-5 years professional experience generally;
Basic understanding of GCP and human subject research regulations;
Proven ability to manage tasks and maintain documentation;
Strong communication interpersonal and organizational skills; and
Proficiency in Microsoft Office and familiarity with electronic data capture system.
Desired but not essential experience/skills:
Experience in medical device digital health or software-enabled clinical studies;
Familiarity with ISO 14155 and SaMD standards;
Prior involvement in investigator meetings or lab-based studies;
Understanding of industry-sponsored research challenges with health system partners;
Awareness of R&D innovation trends and collaboration models; and
Ability to translate clinical workflows into technical specification.
Required Experience:
IC
Employment Type
Full-Time
