About C-search
C-Search Clinical Trials Ltd., established in 2016 by Sima Reuven, who has been working in the field since 2000, is a registered enterprise in Israel specializing in providing regulatory consultancy services to pharmaceutical and biotechnology companies worldwide.
As an overseas representative, our company is crucial in assisting international firms with navigating the intricate local regulations in Israel. We guide companies through the complex landscape of regulatory compliance.
Our range of services includes comprehensive support throughout the planning, organization, and execution phases of clinical trials. Our expertise spans the initial stages of clinical trials, encompassing feasibility studies using Artificial Intelligence, site evaluation visits, submissions to the Ministry of Health (MOH) and Local Ethical Committees, and negotiations for contracts and budgets.
We collaborate closely with local depots to manage the import of ancillary products and Investigational Products into the country, ensuring a smooth and compliant process for our clients.
Sima Reuven | owner
Since starting in the clinical trials industry in 2000, I’ve held various roles, gaining expertise in project management, regulatory compliance, and business development.
My experience spans:
- Comprehensive Drug Development: Understanding the entire lifecycle, from research to regulatory compliance.
- Operational and Strategic Planning: Skilled in project execution, risk assessment, and timeline management.
- Regulatory Compliance: Ensuring adherence to local and international standards.
- Leadership and Business Development: Driving organizational growth and guiding teams through complex projects.
Ofira Moran | PH.D
over two decades of experience in Phase I to IV drug and medical device studies. My expertise spans clinical and regulatory activities with specific focus areas:
- Clinical oversight management
- Monitoring diverse therapeutic areas.
- Managing multi-center trials in the U.S. and Europe.
- Handling study start-ups and regulatory submissions.
- Developing SOPs.
- Preparing safety reports for the FDA.
- Designing CRFs.
- Leading training programs.
My professional roles have included Clinical Oversight Manager, Senior CRA/Project Manager, and Associate Director of Clinical Research.