Clinical Research Associate In Lebanon

Job Description: Clinical Research Associate (CRA)

Main tasks:

• Participation in the creation of the monitoring documents (monitoring guidelines, tracking tools, working documents…)
• Participation in the regulatory submissions (Competent Authorities and Ethics Committee)
• On-site visits: selection, initiation, monitoring, and close-out
• Serious Adverse Event (SAE) declaration and follow-up
• Management of study drugs: drug accountability, returns, storage conditions, resupplies requests…
• Management of the study material
• Investigators Site files preparation, check and update,
• Trial Master File setup and maintenance,
• Study tracking and follow-up tools update
• Case report forms quality control and handling
• Management of queries,
• Communication with the investigational sites,
• Investigators and hospitals contracts management,
• Management of investigator fees and hospital invoices,
• Participation in investigator’s meetingRespect of quality commitments
• Respect for quality commitments
• Participating in the improvement of the Quality System: non-conformities management, review/creation of standard procedures and documents.

Required skills and qualities and expected level:

• Good level of English (spoken and written)Knowledge of GCP and ICH Guidelines
• Knowledge of GCP and ICH Guidelines
• Good command of office software (excel, word, powerpoint)
• Analytical, rigorous and organized
• Good interpersonal skills
• Good oral and written communication
• Ability to summarize.

Required level of education:

• Scientific diploma 4 years diploma research (DIUFARC, DIUFIEC or other…)

Required work experience in this role

• Training course of minimum 6 months as a clinical research associate.