Job Description

1. Responsibilities include overseeing the collection, entry, verification, management, tracking, and reporting of data and other documents related to study management
2. Create data collection forms, error checking methods and related programmes for efficient collection, analysis and reporting;
3. Troubleshoot computer problems;
4. Prepare required study documentation/updates and other required tools for the project;
5. Liaise with study centre personnel, study committee members and other related study personnel;
6. Ensure relevant clinical and research methodology is applied, and proper handling of all clinical research material is used;
7. Train and supervise data clerks and other study staff in the processing of study data (i.e. data entry);
8. Assist with preparations of scientific papers, abstracts and graphs;
9. Perform literature searches.Qualifications1. Bachelor Degree or higher in health related field or previous clinical trial experience in a similar capacity
2. Ability to work independently, excellent communication (both oral and written) and problem solving skills, and ability to work flexible hours .
3. Proficiency in MS Access, Excel, Word, Powerpoint.
4. Previous experience in cardiovascular clinical trials an asset.
5. Experience with Framemaker and DataFax or similar data management software an assetAs a condition of employment, you are required to submit proof of full COVID-19 vaccination to Employee Health Services.

Hamilton Health Sciences