מדעים/ביוטק

Associate Document Specialist

470706

תאריך עדכון

15/10/2020

תיאור המשרה

QUALIFICATIONS:

· bachelor’s degree or nursing qualification is required. Scientific/health care field

preferred, but not required.

· Minimum of 1-year experience in use of eTMF system (e.g. clinical site, CRO, Sponsor or clinical trial

vendor).

· Comfortable with technology and ability to learn new systems quickly.

· Relevant experience in clinical research (clinical operations and/ or QA preferred) or related field.

· Exposure to current regulatory requirements and guidelines governing clinical research and GCP

· Working knowledge of MS Word, Excel, PowerPoint and Outlook.

· Requires attention to detail in composing and proofing materials, establishing priorities, scheduling

and meeting deadlines.

· Must be able to professionally interact and communicate with visitors, vendors and individuals at all

levels of the organization.

Clinical Trial Manager Version 02, 26NOV19

· Must be able to work in a fast-paced environment with demonstrated ability to appropriately

prioritize competing tasks and demands.

· Ability to work proactively and successfully within a cross-functional team.

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