Regulatory and Start Up Specialist

Precision Medicine Group(1 day ago)

AustraliaOnsiteFull TimeMedior$65,307 - $88,805 (estimated)Regulatory Affairs

About this role

Precision for Medicine is seeking a Regulatory and Start Up Specialist to join their growing team. The role involves managing site activation processes, preparing regulatory submissions, and coordinating with multiple key stakeholders to ensure compliance and timely trial start-up.

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Required Skills

Regulatory Submissions
Clinical Trials
Site Activation
Communication
Regulatory Compliance
Project Management
Document Coordination
Local Regulations
IRT System
Start-up Planning

About Precision Medicine Group

precisionmedicinegrp.com

Precision Medicine Group (PMG) is a consulting and solutions firm that helps pharmaceutical and life‑science companies accelerate drug development and improve patient outcomes by applying the discipline of precision medicine. PMG brings together specialized expertise in data and evidence generation, manufacturing, market access, and stakeholder engagement to unlock insights and speed commercialization. Focused on delivering measurable value, the company partners with innovators to advance development, strengthen access, and "move science closer to health."

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