iAM Jobs

 

• Assistance in the management and monitoring of clinical studies with the hospital teams
• Routine and on-going monitoring of the clinical data and the study progress
• Writing and updating study documents (e.g protocol, Investigator brochure , informed consent forms, etc.), SOPs, management and progress reports
• Communication and supervision of study vendors

• CRA certification (ICH-GCP course)
• At Least one year experience CRA (priority for pharma and CRO companies)
• At least a bachelor's degree in life sciences, biomedicine or any other relevant field
• Fluent English (reading, writing and speaking)
• Excellent skills in Microsoft Office programs (Excel, Word, PowerPoint)
• knowledge in safety data management and data coding- will be an advantage
• Driving License
• Residence in Haifa area