At a Glance
- Tasks: Manage regulatory submissions and site activation activities across various sites.
- Company: Join Precision Medicine Group, a leader in innovative healthcare solutions.
- Benefits: Competitive salary, flexible work options, and opportunities for professional growth.
- Other info: Exciting role with potential for career advancement in a fast-paced environment.
- Why this job: Make a real difference in the healthcare industry while working with a dynamic team.
- Qualifications: Experience in regulatory submissions and strong organisational skills required.
The predicted salary is between 82800 - 101200 $ per year.
Precision Medicine Group seeks a Regulatory and Site Start Up Specialist in Australia to manage regulatory submissions and site activation activities across assigned sites.
You will prepare CTAs and dossiers for competent authorities and ethics committees, maintain essential documents, and collaborate with CRAs to ensure timely site activation.
You will support feasibility, budgeting, and guidance to in-country teams while staying compliant with local and international regulations.
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Global Regulatory & Site Start-Up Expert in Sydney employer: Precision Medicine Group
At Precision for Medicine, we pride ourselves on being an exceptional employer that fosters a collaborative and innovative work culture. Our commitment to employee growth is evident through ongoing training and development opportunities, particularly in the dynamic fields of Oncology and Rare Disease. Located in a vibrant area, we offer a supportive environment where team members can thrive while making a meaningful impact on the future of life sciences.
