Related skills
gcp edc cro irt ecoa📋 Description
- Manage global clinical trial programs (Phases I-III).
- Ensure GCP/SOP and regulatory compliance.
- Partner with CROs/vendors for milestones and budgets.
- Ensure data quality for regulatory submissions.
- Communicate project status with stakeholders.
- Identify and mitigate trial risks.
🎯 Requirements
- Bachelor's in life science or equivalent.
- 5+ years in international clinical trial mgmt.
- Prior Phase II/III experience required.
- Knowledge of drug development, ICH, and GCP.
- Proven CRO/vendor oversight experience.
- Strong leadership in fast-paced, cross-functional teams.
🎁 Benefits
- CORE values culture: Caring, Original, Resilient.
- Fast-paced environment with growth opportunities.
- Competitive pay and equity opportunities.
- Generous PTO, company shutdowns, and paid sick leave.
- Professional development resources.
- Regular all-team in-person meetings.
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