At a Glance
- Tasks: Support site management and monitor clinical trials while ensuring compliance.
- Company: Emerald Clinical, a leader in clinical research with a focus on innovation.
- Benefits: Hybrid/remote work options, competitive salary, and professional development opportunities.
- Other info: Exciting opportunity for career growth in a supportive environment.
- Why this job: Join a dynamic team and contribute to groundbreaking clinical research projects.
- Qualifications: 2+ years of on-site experience and strong ICH-GCP knowledge required.
The predicted salary is between 66150 - 80850 $ per year.
Emerald Clinical is seeking a Clinical Research Associate 2 in Melbourne.
The role sits within Clinical Operations, supporting site management, monitoring activities, and regulatory package preparation to ensure trial compliance.
You will coordinate investigator and site feasibility, conduct initiation and monitoring visits, and train site staff while maintaining trial documents and TMF integrity.
A strong ICH-GCP background and 2+ years of on-site experience are expected.
Global Clinical Research Associate – Hybrid/Remote in Melbourne employer: Emerald Clinical
Emerald Clinical Trials is an exceptional employer, dedicated to transforming clinical research while prioritising the wellbeing of both patients and employees. With a strong focus on purpose-driven work, competitive compensation, and flexible working arrangements, we foster a collaborative culture that values innovation and diverse perspectives. Join us in making a real impact on global health, with ample opportunities for career growth and development within a supportive environment.
