
Responsibilities:
· Participate and complete Junior CRA training Curriculum
· Schedules, plans, and performs site visits according to the monitoring plan and SOPs to ensure appropriate site visit activities are completed at each onsite or remote visit with the close supervision of the Clinical Operations Manager
· Under Clinical Operations Manager supervision, supports on assigned trials by tracking Submission, approvals, recruitment and data cleaning activities.
· Under Clinical Operations Manager supervision, communicates with sites on assigned trials to manage trial milestones and issues.
· Under Clinical Operations Manager supervision, assures adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures
· Maintains Investigator Site File (ISF) up to date as well as all other clinical trial documents
Requirements:
· Holds a Bachelor Degree, or equivalent, in a scientific/medical discipline
· Minimum 2 years of experience
· Enthusiastic, motivated and able to work independently and communicate with a variety of healthcare professionals at monitoring sites
· Deals with confidential information and/or issues using discretion and judgment
· Basic good knowledge and ability to apply ICH/GCP and any other applicable international guidelines, applicable local regulatory guidelines and Standard Operating Procedures
· Valid Driver’s License where applicable
· Strong attention to detail
· Effective time management skills
· Proven flexibility and adaptability
· Effective verbal and written communication skills, with the ability to communicate effectively with medical personnel
· Good computer skills: good knowledge of Microsoft Office
· Proficiency in English and French
· Flexibility to travel
[email protected] |***********| 
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