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.
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📌 Regulatory Start Up Specialist Ii: Accelerate Trial Approvals Melbourne (Australia)
🏢 Novotech
📍 Australia
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