Submission Specialist Assistant Regulatory Department
Posted on :
22-01-2025
Employer Active
1 Vacancy
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Job Description
Join our international team and support regulatory aspects of clinical research projects streamlining communication maintaining electronic systems and managing documents.
OfficeBased in Raanana
You will:
- Be the point of contact for clinical project teams and support services on regulatory matters
- Prepare draft regulatory/ethics submission dossier
- Be responsible for document management such as filing processing translation quality control
- Update and maintain (automated) tracking systems working files and schedules
- Organize meetings prepare agendas and minutes
Qualifications :
- College/University degree or an equivalent combination of education training & experience
- Life Science degree is a plus
- Administrative work experience preferably in an international setting
- Prior experience in Clinical Research is a plus ideally as a Site Coordinator or Submission Assistant/Clinical Trial Administrator at a CRO
- Full working proficiency in English and Hebrew
- Proficiency in MS Office applications
- Ability to plan multitask and work in a dynamic team environment
- Communication and collaboration skills
Additional Information :
Advance your career in clinical research coordinating a variety of tasks and learning new things while growing with the company.
Remote Work :
No
Employment Type :
Fulltime
Employment Type
Full-time
Key Skills
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