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运动公司 Data Manager
Job in
Richmond Hill, Ontario, Canada
Listed on 2026-07-07
Listing for:
Intscanada
Full Time
position Listed on 2026-07-07
Job specializations:
-
IT/Tech
Data Analyst, Data Engineering
Job Description & How to Apply Below
RESPONSIBILITIES RELATED TO PROJECT INITIATION
Effective management of all data and reports (management reports and/or clinical data reports) based on project protocol and overall information objectives
Assist with implementation and testing of eCRF and reports into Axiom Aware or Axiom Go Cubed Data Capture & Reporting Tools
Develop key Data Management documents for presentation to and review by the sponsor
Assist where applicable in the development and implementation of site training and ongoing data management related support plans
RESPONSIBILITIES RELATED TO PROJECT MAINTENANCE
Responsibility for all aspects of data management for each study, including issue and resolution of queries where applicable
Responsible for ensuring data integrity, the performance of edit checks, and recommending applicable changes/updates to the Data Integrity Plan as per Sponsor request/Protocol amendments and/or eCRF updates
Follow up on eCRF and query completion with sites
Evaluate and add queries to data where applicable based on edit check output
Responsible for data transfer configuration and quality assurance of data transfer validation activities
Remote site training, support, and communications from a data management perspective
Ongoing support for the management of the project and associated ancillary initiatives (e.g. newsletters, data abstracts/manuscripts/presentations, public awareness activities, project expansion, assisting with interim analyses, database lock and coding, etc)
Assist, where applicable, with the maintenance of the Axiom Aware or Axiom Go Cubed Clinical Trial Suite application in conjunction with the Project Manager
RESPONSIBILITIES THROUGHOUT LIFECYCLE OF A PROJECT
Data management and data quality assurance
Close, ongoing collaboration with members of the project team to ensure the project runs smoothly and efficiently and that overall strategic objectives are realized
Qualifications
3–5 years’ experience in CRO, Biotech, or Pharmaceuticals
Working knowledge of clinical, medical, and biology domains
Proficiency in Microsoft Word, Excel, PowerPoint, Project, and Outlook
Knowledge of ICH-GCP
Experience with EDC systems (data entry and/or configuration)
Enthusiastic, smart, resourceful, analytical
Well‑developed written and communication skills
Perceptive listening skills
Strong attention to detail
Time management skills
Ability to work independently within a team environment
Adept at multi‑tasking
Basic understanding of web‑based technologies and browsers
or recognized equivalent in a Health or Science related field
Benefits
Dental care
Extended health care
Life insurance
Paid time off
Vision care
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