At a Glance
- Tasks: Manage regulatory submissions and site interactions for timely study initiation.
- Company: Caidya, a leader in clinical research with a focus on innovation.
- Benefits: Flexible remote work, competitive salary, and opportunities for professional growth.
- Other info: Join a dynamic team dedicated to making a difference in clinical studies.
- Why this job: Be part of impactful research that shapes the future of healthcare.
- Qualifications: Experience in regulatory processes and strong organisational skills.
The predicted salary is between 63000 - 77000 $ per year.
Caidya is seeking a Study Start-Up Country Specialist II (ROW) to support Australia-based country start-up activities.
You will manage regulatory submissions, translations, and site interactions to ensure timely study initiation.
Working with the SSU Manager and project teams, you will coordinate CDA processes, review essential documents, and track submission status across assigned countries in accordance with ICH-GCP and local regulations.
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ROW Study Start-Up Specialist II – Remote in Canberra employer: Caidya
As a Study Start-Up Country Specialist II at our company, you will thrive in a supportive and collaborative work culture that values your expertise and fosters professional growth. With opportunities for mentorship and coaching, you will be part of a dynamic team dedicated to advancing clinical research in Australia, while enjoying the flexibility of a home-based role that promotes work-life balance and personal well-being.
