Work Flexibility: Hybrid
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. You’ll 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. You’re detail-oriented, organised, and thrive in collaborative environments. You’re 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:
- Bachelor’s 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;
- Solid 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.
Travel Percentage: 10%