Reports Submissions Supervisor


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:


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