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.
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:
Clinical Trials and Regulatory Affairs Specialist with over 20 years of diverse experience across clinical research, regulatory submissions, and project management. Proven ability to lead complex, multi-center clinical trials from start-up to close-out, with a therapeutic focus spanning Ophthalmology, Oncology, Neurology, Gastroenterology, Cardiology, Psychiatry, Gynecology, Infectious Diseases, and wound care.
Experienced in a variety of roles, including Start-Up Specialist, Senior Clinical Research Associate (CRA), Clinical Oversight Manager, Associate Director of Clinical Research, and Freelance Project Manager. Successfully collaborated with global pharmaceutical companies, biotech firms, and CROs.
Highly skilled in managing Ministry of Health (MOH) and Ethics Committee (EC) submissions in Israel, with strong knowledge of European regulatory environments and international guidelines. Known for ensuring regulatory compliance, conducting clinical monitoring, managing vendor and site relationships, and maintaining subject safety and data integrity.
Proficient in developing training materials, overseeing clinical documentation, supporting audit readiness, and facilitating collaboration between study teams and stakeholders. Experienced in both remote and on-site environments, bringing flexibility, precision, and strong organizational skills to every project.
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