Sponsor dedicated Site Activation Specialist II - Hybrid Based in Kfar-Saba
Clinical Careers Page(7 days ago)
About this role
This role involves supporting site activation and start-up activities for clinical trials within a biopharmaceutical organization. The position requires coordination with various stakeholders to ensure timely delivery of project milestones at the country level, focusing on document submissions, regulatory compliance, and site readiness.
Required Skills
- Regulatory Submissions
- Clinical Trial Management
- Site Activation
- Documentation
- Project Coordination
- Regulatory Affairs
- Quality Assurance
- Vendor Management
- Trial Master File
- Data Protection
Qualifications
- Bachelor's Degree
- 2+ years of Site Activation experience
About Clinical Careers Page
syneoshealth.comSyneos Health is a biopharma solutions organization and full‑service contract research organization (CRO) that integrates clinical development, regulatory and commercialization services to help life‑science companies bring therapies to market faster. It provides end‑to‑end capabilities — clinical trials across phases and therapeutic areas, real‑world evidence and data analytics, medical affairs, market access, patient engagement and commercial launch services. With a global network of scientific, clinical and commercial experts, Syneos partners with biopharma, biotech and medtech clients to de‑risk development programs and accelerate product adoption.
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