לוח אפשרויות קריירה - הדרך החכמה להייטק

a global medical device comany is looking for an experienced clinical project manager to to join our clinical team and take part in planning clinical trials.


Duties and Responsibilities:
"Serve as a liaison between the company and the study site, investigators, study coordinators, and staff members
"Coordinate activities to set up and monitor a study from site initiation to study closeout (including preparation of study plans, budget, clinical sites coordination, etc.)
"Prepare ethical submissions, study documents (protocols and informed consent forms, case report form) and investigator brochures for clinical studies
"Perform monitoring visits as well as remote data monitoring
"Create and review monitoring visit reports
"Perform training visits at clinical sites
דרישות:
BSc/MSc Degree in Life Sciences, Nursing or Biomedical Engineering
CRA certificate
At least 3 years' experience as a CRA in a medical device company
Knowledge of standards and regulation of clinical trials in USA, Europe and Israel
Knowledge of computer systems for managing and reporting clinical studies (eCRF)
Ability to analyze data and write test reports
Strong team player skills
Excellent presentation and communication skills – in Hebrew and English