Novotech in Melbourne is seeking a Regulatory Start-Up Associate II to plan, prepare and review country- and site-level submissions for clinical trials, ensuring alignment with ICH-GCP and local rules. The role emphasizes proactive start-up activities and effective stakeholder coordination.
The RSA II will support RSM/PM and sites, manage submission timelines, and produce accurate regulatory packages for ethical and regulatory authorities.
Regulatory Start-Up Specialist II: Accelerate Trial Approvals in Melbourne 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.
