Site Management Associate (Clinical Trials)
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About the role
Office-based Site Management Associate role in Ra'anana supporting clinical research projects for an international CRO. Responsibilities include site communication, document and Trial Master File management, clinical supplies, regulatory and ethics submissions, safety information flow, audits, payments, and CTMS updates. Requires a college/university degree in Life Sciences, prior clinical research or CRO administrative experience, Hebrew and English proficiency, and Microsoft Office skills.
Key requirements
- • College/University Degree (Life Sciences)
- • Required skills: Prior administrative experience in Clinical Research or a CRO environment, Full working proficiency in Hebrew, Good English skills, Proficiency in Microsoft Word, Excel and PowerPoint, Organizational and planning skills, Problem-solving abilities, Ability to multitask in a fast-paced environment, Teamwork and interpersonal skills
- • Required languages: Hebrew, English
Opportunity details
- • Workplace: On Site
- • Posted: Oct 28, 2026
- • Original advert language: English
Full vacancy
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See original vacancy ↗Employer’s role description
Job title: Site Management Associate (Clinical Trials)
Location: Ra'anana, Center District, Israel
Employment type: Full-time
Company Description
PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.