EPM Scientific is partnering with a global medical device organisation seeking experienced freelance Clinical Research Associates to support clinical studies across Australia.

Key Requirements

- Solid background in clinical research within medical devices

- Experience supporting and/or monitoring clinical trials from start-up through close-out, including site activation, regulatory submissions, and study maintenance activities

- Knowledge of ICH-GCP, ISO 14155, and applicable local regulatory requirements

- Experience working with clinical sites, Ethics Committees, and study documentation (eTMF, CTMS, regulatory files)

- Strong stakeholder management and communication skills

- Fluent in English

Responsibilities

- Support site start-up, regulatory submissions, site activation, enrollment, follow-up, and close-out activities

- Ensure study documentation is accurate, complete,



and inspection-ready throughout the study lifecycle

- Act as the primary liaison between study teams, sites, and cross-functional stakeholders

- Monitor study progress, identify risks, and support successful trial delivery

- Maintain compliance with ICH-GCP, ISO 14155, SOPs, and local regulations

Contract Details

- Start Date: Jan 2027

- Location: Australia (Remote)

- Contract Type: Freelance

- Commitment: 1.0 FTE

- Duration: Initial 12-month contract with strong possibility of extension

- Rate: Competitive hourly rate, dependent on experience

If you're interested, please apply with your CV. If this opportunity isn't suitable for you, feel free to share it with your network.

📌 Freelance Clinical Research Associate (m/f/d) (Australia)
🏢 Epm Scientific
📍 Australia