At a Glance
- Tasks: Plan and review regulatory submissions for clinical trials, ensuring compliance and timely approvals.
- Company: Join Novotech, a leader in clinical trial services with a focus on innovation.
- Benefits: Enjoy competitive pay, flexible work options, and opportunities for professional growth.
- Other info: Be part of a dynamic team driving impactful projects in the clinical research field.
- Why this job: Make a difference in healthcare by facilitating crucial clinical trial approvals.
- Qualifications: Experience in regulatory submissions and strong organisational skills are essential.
The predicted salary is between 67500 - 82500 $ per year.
Novotech is seeking a Regulatory Start-Up Associate II to plan, prepare, and review country- and site-level ethics and regulatory submissions during the start-up phase of clinical trials. The role ensures compliance with ICH-GCP and local regulations while coordinating with the Regulatory Start Up Manager (RSM), Project Manager, and sites to drive timely approvals.
You will manage submission deadlines, provide local regulatory insights, and uphold submission timelines across country and site.
Regulatory Start-Up Associate II in Sydney employer: Novotech
Novotech is an exceptional employer that fosters a dynamic and collaborative work culture, perfect for those passionate about advancing their careers in toxicology and regulatory affairs. Located in Australia, we offer our employees comprehensive growth opportunities, competitive benefits, and the chance to work alongside industry experts on cutting-edge projects in clinical trials. Join us to make a meaningful impact in the field while enjoying a supportive environment that values innovation and professional development.
