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microsoft office budget management clinical trial management cro ich-gcpπ Description
- Lead cross-functional teams and oversee complex clinical trials.
- Manage all project-specific services (central labs, shipments, etc.).
- Ensure project development aligns with contracts, SOPs, ICH-GCP, and regulations.
- Monitor timelines, budgets, and sponsor/investigator communications.
- Maintain up-to-date knowledge of scientific, regulatory, and operational aspects.
π― Requirements
- Bachelor's Degree in scientific/medical fields; nursing or related degree preferred.
- Eight+ years of clinical research experience in project management.
- Previous CRO experience required; hematology/oncology studies preferred.
- Previous CRA experience is highly desirable.
- Strong knowledge of clinical trial operations, GCP/ICH guidelines.
- Proficiency in MS Office; fluent in English; EDC experience preferred.
π Benefits
- Remote opportunity with potential hybrid arrangement.
- Global team with opportunities across multiple regions.
- Strong work-life balance and collaborative culture.
- Professional development and ongoing training.
- Exposure to hematology/oncology trials across a CRO.
- Join a global CRO focused on delivering high-quality results.
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