Join our team of experts in regulatory and ethics submissions of clinical studies. You will focus on facilitating the start of research projects of novel medicinal products, while taking a step further in your professional career.
Office-based role in Ra'anana , Israel
You will:
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Prepare clinical trial submission dossiers for Regulatory Authorities and Ethics Committees
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Communicate with regulatory authorities, ethics committees, project teams and vendors on regulatory-related matters
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Review translations of essential documents subject to clinical trial submission
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Track the regulatory project documentation flow
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Review documents to greenlight IP release to sites
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Manage safety reporting to authorities
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Deliver regulatory training to project teams
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Assist with feasibility research and business development requests
- College/University degree or an equivalent combination of education, training and experience. Life science degree is a plus
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Prior experience of at least one year with clinical trial submissions in Israel within the CRO or Pharmaceutical industries
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Full working proficiency in English and Hebrew
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Proficiency in MS Office applications and `Matarot’ software
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Detail-oriented
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Ability to learn, plan and work in a dynamic team environment
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Communication, collaboration, and problem-solving skills
- Please send your CV in English
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.
We offer:
- Excellent working conditions
- Extensive training and friendly team
- Competitive salary and benefits package
- Opportunities for personal and professional growth
Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.