Reg & Start Up Coordinator / Specialist


Under direction of line manager, support the delivery of activities as determined by the appropriate country, regional lead or global lead. May conduct specific tasks under guidance of senior staff. Responsibilities may include all or some of the activities listed at any one time.


Assist the team in the preparation, handling, distribution, filing and archiving of documentation according to the scope of work and standard operating procedures

Review documents for completeness, consistency and accuracy, under guidance of senior staff

Prepare client deliverable documents using appropriate tools and may draft text for straightforward documents, under guidance of senior staff

Assist with completion of relevant Clinical Trial Management System (CTMS) fields, databases, tracking tools, timelines and project plans with project specific information

Provide support for administrative tasks, e.g. meeting coordination, minute taking, travel arrangements, faxing, copying, couriers

Interact with internal and external clients, under guidance of senior staff

May perform IP release activities on small, straightforward projects or support reviews for larger projects


CRA course, with profound knowledge in ICH-GCP

At least few months experience as Study Coordinator

Experience with Ethic Committee submission preparations

Individual learning ability, ability to work independently and also within a team

Very high level of English and Hebrew

Excellent interpersonal skills

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