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Un centre de recherche biomédicale renommé à Montréal recherche un(e) candidat(e) pour effectuer des activités de saisie de données pour des études de recherche clinique. Le poste exige un diplôme DEC, une expérience en milieu clinique, ainsi que la capacité à travailler de manière autonome et en équipe. Les compétences requises comprennent la maîtrise de MS Office et la discrétion dans le traitement des informations confidentielles.
Le Centre universitaire de santé McGill (CUSM) est un centre hospitalier universitaire intégré reconnu à l'échelle internationale pour l'excellence de ses programmes cliniques, de sa recherche et de son enseignement. Le CUSM a pour objectif d'assurer aux patients des soins fondés sur les connaissances les plus avancées dans le domaine de la santé et de contribuer au progrès des connaissances.
RESEARCH INSTITUTE OF THE MUHC
The Research Institute of the McGill University Health Centre (RI-MUHC) is a world-renowned biomedical and hospital research centre. Located in Montreal Quebec the Institute is the research arm of the McGill University Health Centre (MUHC) affiliated with the Faculty of Medicine at McGill University. The RI-MUHC is supported in part by the Fonds de recherche du Québec – Santé (FRQS).
Under the supervision of the Centre for Innovative Medicine (CIM) Manager the incumbent will conduct data entry activities for clinical research studies.
Collects clinical data as well as patient information
Conducts and / or verifies study document information
Performs data entry as required by the protocol
Ensures compliance with protocol guidelines and requirements of regulatory agencies
Identifies problems and / or inconsistencies and provide solutions
Remits weekly updates to his immediate supervisor on the status of the data entry for all studies.
Accomplishes any other administrative tasks as required by the immediate superior or delegate.
/ Experience
DEC diploma
Experience in a hospital / clinical setting is preferred
Experience in oncology is preferred
Experience in clinical research is preferred.
Ability to display a high degree of discretion in dealing with confidential information
Knowledge of international federal and provincial laws and regulations governing clinical research is an asset ICH-GCP HC DIV5
Bilingual (French and English)
Excellent organization ability to multitask and prioritize time-sensitive issues
Excellent interpersonal skills
Solid written and verbal communication skills
Ability to work under minimal supervision
Resourceful and responsible
Highly proficient in MS Office (Word Excel)
Electronic data capture (EDC) system knowledge is an asset
Ability to problem solve
Must be a team player.
Databases,Computer Hardware,Typing,Microsoft Office,Data Entry,Computer Skills,Microsoft Word,Office Experience,10 Key Calculator,Microsoft Excel,Order Entry,Word Processing
Unclear
years
1