Clinical Research Associate (CRA)

JOB #

4025

Job Description

Clinical Research Associate (CRA) is responsible for the end-to-end smooth execution of the clinical and preclinical studies that are conducted by and for the company and is an active participant in the local study team(s). The CRA is the main contact with all the relevant stakeholders of the study: site, regulatory, outsource companies, physicians, scientists, patients, installations, committees, etc

Responsibilities

  • end-to-end administration of preclinical and clinical studies
  • developing, tracking and resolving the projects plan and study specific documents and timeline
  • planning and executing the study, including relevant approvals, special needed
  • presenting the company, where appropriate , to regulatory authorities in the context of the study
  • interfacing with relevant stakeholders , inc. external service providers to support effective execution of the study
  • interfacing with patients, physicians and other relevant stakeholders, in accordance to the regulatory demands of the study and familiarity with the relevant and local regulatory demands to conduct a specific study
  • responsibility for the study materials and equipment
  • auditing and regulatory inspecting the work of external service providers and other reassure the execution of the study
  • leading the study-related activity from preparation to end of internal and external meetings and presentations, reports, etc
  • ensuring compliance with ethics and local , national and regional legislation , as applicable

Requirements

  • BSc with 5+ years of experience as a CRA or MSc with 3+ years of experience as a CRA. Degree in related discipline, preferably in life science , or equivalent qualification
  • Ability to process the data acquired in the study and provide comprehensive overview to the company’s management team
  • good knowledge of relevant local regulations in Israel; familiarity with additional regional regulations is a plus
  • languages : English & Hebrew, excellent verbal and written communication
  • good understanding of Clinical Study Management including monitoring and data management
  • excellent attention to details
  • valid driving license \ability to travel nationally

Desirable

  • team oriented and flexible ;ability to respond quickly to shifting demands and opportunities
  • excellent communication skills
  • ability to work in an environment of remote collaborators
  • good analytical and problem solving skills
  • demonstrated ability to prioritize and manage multiple tasks with conflicting deadlines
  • familiarity with current imaging industry assessment criteria standards and techniques - a significant advantage

Send your CV to HR@nanox.vision