Supervise the Report Production activities & staff;
Provide training and support as required to the various departments generating study data and to Report Production staff;
Interact with MIS Personnel in order to create tools to populate standard templates with the data generated by the various sources;
Interact with the Scientific Departments in order to implement the terminology required by the Reports standards and to create standard formatting for the various data sources;
Determine and analyze the source of data required in the reports;
Other elated tasks;
Very analytic and detail oriented person;
Excellent communication skills;
Proven experience establishing positive relationships within the workplace;
Ability to take on a leadership role;
Focused and well-organized;
Proficient in MS Office (Word, Excel, Outlook);
Experience with preclinical data collection systems and practices is an important asset;
In-depth understanding of preclinical data( is an important asset).
Exposure to industry data standards and terminologies (e.g., CDISC data standards) is an important asset;
English is a must, bilingual English and French is an Asset;
Please note that this is a full time 37.5/h a week, one year contract with a possibility of extension & permanency.
Start Date: ASAP
Please send your CV to: firstname.lastname@example.org
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