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Biotech
Lead product strategy and development for data management solutions in life sciences, ensuring market relevance and user satisfaction while managing lifecycle and stakeholder alignment.
Biotech
Manage and oversee regulatory authority, IRB/EC, and Third Body submissions for clinical site readiness. Plan submission strategy and timelines, ensure compliance with regulations, support CTIS/EU CTR activities, coordinate with local teams, track milestones, support audits, mentor junior staff, and contribute to process improvements and project financial management.
