Clinical Research Associate II: Translating Breakthroughs for Global Patient Outcomes
3 days ago
Company Overview
SYD Fortrea Australia Pty Ltd is a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience. We provide pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas.
We have over 19,000 staff conducting operations in more than 90 countries, transforming drug and device development for partners and patients across the globe.
Salary Information
The estimated salary for this role is AUD $120,000 - $150,000 per annum, depending on experience and qualifications.
Job Description
As a Clinical Research Associate II (CRA2) at SYD Fortrea Australia Pty Ltd, you will be at the forefront of global clinical trials, ensuring compliance and maintaining top-tier data integrity.
This role involves:
- Monitoring clinical trials to ensure studies adhere to protocols, amendments, and regulatory requirements;
- Conducting site visits, including pre-study, initiation, routine monitoring, and close-out visits;
- Managing study sites, tracking regulatory submissions, recruitment, CRF completion, and data query resolution;
- Liaising with sponsors, investigators, and stakeholders for smooth trial execution;
- Ensuring accurate data collection, documentation, and report submissions;
- Assisting in creating and reviewing study protocols, CRFs, and informed consent forms;
- Providing training to site staff for compliance with trial protocols and objectives;
- Evaluating and managing risks to ensure trial integrity and participant safety.
Required Skills and Qualifications
To be successful in this role, you will need:
- A Bachelor's degree in a scientific or health-related field (advanced degree preferred);
- Confidence in clinical research site management and monitoring, ideally within a CRO or pharmaceutical setting;
- Strong understanding of ICH-GCP guidelines and clinical trial regulatory requirements;
- Proven success in monitoring Oncology phase I, II, or III global studies;
- Excellent communication, organizational, and time management abilities;
- Willingness to travel as needed for site monitoring.
Benefits
We offer a dynamic and supportive work environment, with opportunities for career growth and professional development.
Why Choose Us?
At SYD Fortrea Australia Pty Ltd, we are committed to revolutionizing healthcare through cutting-edge research, innovation, and an unwavering commitment to excellence.
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Sydney, New South Wales, Australia SYD Fortrea Australia Pty Ltd Full timeAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
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