Administrative Support III
- AB, Canada
- Edmonton, AB, Canada
Classification: Administrative Support III Union: AUPE GSS Unit and Program: Clinical Trial Unit Primary Location: U of A Hospital Location Details: As Per Location Multi-Site: Not Applicable FTE: 1.00 Posting End Date: 09-NOV-2026 Temporary Employee Class: Temp F/T Benefits Date Available: 07-DEC-2026 Temporary End Date: 03-DEC-2027 Hours per Shift: 7.75 Length of Shift in weeks: 2 Shifts per cycle: 10 Shift Pattern: Days Days Off: Saturday/Sunday Minimum Salary: $25.72 Maximum Salary: $31.25 Vehicle Requirement: Not Applicable · Temporary
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Job details
- Pay
- Classification: Administrative Support III Union: AUPE GSS Unit and Program: Clinical Trial Unit Primary Location: U of A Hospital Location Details: As Per Location Multi-Site: Not Applicable FTE: 1.00 Posting End Date: 09-NOV-2026 Temporary Employee Class: Temp F/T Benefits Date Available: 07-DEC-2026 Temporary End Date: 03-DEC-2027 Hours per Shift: 7.75 Length of Shift in weeks: 2 Shifts per cycle: 10 Shift Pattern: Days Days Off: Saturday/Sunday Minimum Salary: $25.72 Maximum Salary: $31.25 Vehicle Requirement: Not Applicable
- Job type
- Temporary
- Apply by
- Experience
- Proficient in Microsoft Office and Excel. 1-2 years experience working in a gastroenterology clinical trial environment.
- Posting language
- English
- Posted
Original job description
The Clinical Trial Unit is recruiting an Administrative Support III to join our research team, you will be assigned to the Gastrointestinal and Liver Research Group (GILDR) located at the Zeidler Ledcor Centre. In this Administrative position, you will utilize clinical research knowledge and skills to perform varied and specialized duties associated with the initiation, organization, and documentation of clinical and research trials. The ability to prioritize your daily workload and work under minimal guidance is important to be successful in this role. Some specific assignments may include assisting with the preparation of mandatory Health Canada regulatory documents, circulating and tracking protocol training documents and study amendments, Process, printing and filing of IND reports, assist with updating processes and SOP’s. Additionally, you may be required to prepare central lab kits, transport blood and/or specimens to the lab and discarding trial specific supplies. Clerical duties in this position may include but not limited to; document filing, scheduling site initiation visits, monitoring visits and other meetings as required, data entry, assist with creation of participant source documents, printing & scanning, and ordering of clinical/office supplies. Archiving of study documents at the end of the study.
Description:
As an Administrative Support III, you will require advanced administrative or specialized skills and knowledge to support complex procedures, practices and initiatives within a department or program.
Classification: Administrative Support III Union: AUPE GSS Unit and Program: Clinical Trial Unit Primary Location: U of A Hospital Location Details: As Per Location Multi-Site: Not Applicable FTE: 1.00 Posting End Date: 09-NOV-2026 Temporary Employee Class: Temp F/T Benefits Date Available: 07-DEC-2026 Temporary End Date: 03-DEC-2027 Hours per Shift: 7.75 Length of Shift in weeks: 2 Shifts per cycle: 10 Shift Pattern: Days Days Off: Saturday/Sunday Minimum Salary: $25.72 Maximum Salary: $31.25 Vehicle Requirement: Not Applicable
Required Qualifications:
Completion of Grade 12 or equivalent.
Additional Required Qualifications:
Proficient in Microsoft Office and Excel. 1-2 years experience working in a gastroenterology clinical trial environment. Knowledge of Electronic Data Capture systems specifically Medidata Rave. Experience in preparation of Regulatory Documents, Investigator File Set up and archiving study documents. Connect Care experience to upload ICFs and other research related documents. Knowledge of Investigational Product Storage requirements. Current GCP and Health Canada Division 5 Certificate. Strong communication and interpersonal skills. Ability to multi-task effectively. Must be able to lift and transport large volumes of charts, binders, lab kits, boxes etc. to various areas on a regular basis, and push/pull loaded carts. Physical demands of the job include sitting for extended periods, lifting and transporting office/medical supplies and equipment weighing up to 40 lbs., and using repetitive motions, lifting, bending, reaching and standing for prolonged periods.
Preferred Qualifications:
As Required.
More about this job
Responsibilities
Support the initiation, organization, and documentation of clinical and research trials, including preparing regulatory documents, tracking training and amendments, processing reports, and maintaining study files. Perform clerical and operational tasks such as scheduling visits, data entry, preparing lab kits, transporting specimens, ordering supplies, and archiving study documents.
Requirements
Requires Grade 12 or equivalent, proficiency in Microsoft Office and Excel, and 1–2 years of experience in a gastroenterology clinical trial environment. Candidates must have experience with Medidata Rave, regulatory documents, investigator files, archiving, Connect Care, investigational product storage, and current GCP and Health Canada Division 5 certification, along with strong communication and multitasking abilities.
Skills
- Clinical Trial Administration
- Investigator File Setup
- Study Document Archiving
- Microsoft Office
- Microsoft Excel
- Medidata Rave
- Connect Care
- Good Clinical Practice
- Health Canada Division 5
- Protocol Training Tracking
- Data Entry
- Scheduling
- Document Management
- Communication
- Multitasking
Visa sponsorship
Not detected in the job text
Categories
- Administrative
- Healthcare
- Science & Research
Keywords
- Clinical Trials
- Gastroenterology
- Liver Research
- Health Canada
- Regulatory Documents
- Investigator Files
- Study Archiving
- Medidata Rave
- Electronic Data Capture
- Connect Care
- Good Clinical Practice
- Health Canada Division 5
- Investigational Product Storage
- Protocol Amendments
- Protocol Training
- IND Reports
- Standard Operating Procedures
- Informed Consent Forms
- Source Documents
- Data Entry
- Central Lab Kits
- Specimen Transport
- Microsoft Office
- Microsoft Excel
- Site Initiation Visits
- Monitoring Visits
- Clinical Research