Clinical Study Manager


Manages the overall planning, conduct and progress of clinical studies, and clinical operation.  The CSM carry the responsibility for making sure the trial is planned and conducted under strict guidelines according to study protocol and regulation and according to company needs and timelines  REPORTS TO: Director of clinical and regulatory affairs

דרישות

 Eperience as a study manager for medical device company or related field. Academic degree in life sciences. Extensive knowledge of ICH/GCP/ISO14155 regulations and guidelines CRA certificate Full working proficiency in English Experienced with Electronic Data Capture (EDC). Proficient in Microsoft Office including Excel, PowerPoint and MS Project.  Willing to travel abroad 15% of the time


Featured Posts
Recent Posts
Archive
Search By Tags
Follow Us
  • Facebook Basic Square
  • Twitter Basic Square
  • Google+ Basic Square

צור קשר

0544577278

עיקבו אחרינו

כל הזכויות שמורות לדפנה לרמן דביר ,אין לעשות שימוש בתוכן האתר ו/או בתמונות המופיעות בו.