Description:As a Research I, you will be working with research teams which are generating and disseminating new knowledge that assists with advancing the understanding of health disciplines and various health and medical concerns. Working under the guidance of the principal investigator, you will be responsible for preparing and submitting research documents, collecting and reviewing a variety of information related to the study, and monitoring study compliance. You will also assist with the recruitment of study participants and initiate consenting of study and/or trial participants and may complete lab work to support research activities.
- Transition Company: Cancer Care Alberta
- Classification: Research I
- Union: HSAA Facility PROF/TECH
- Unit and Program: Owerko Center for Clinical Trials
- Primary Location: Arthur Child Cancer Centre
- Location Details: As Per Location
- Multi-Site: Not Applicable
- FTE: 1.00
- Posting End Date: 17-NOV-2026
- Employee Class: Regular Full Time
- Date Available: 27-NOV-2026
- Hours per Shift: 7.75
- Length of Shift in weeks: 2
- Shifts per cycle: 10
- Shift Pattern: Days
- Days Off: Saturday/Sunday
- Minimum Salary: $38.80
- Maximum Salary: $51.16
- Vehicle Requirement: Not Applicable
Required Qualifications: Diploma or degree in a health or science related field. Registration with applicable professional association or college where required.
Additional Required Qualifications: Minimum of 2 years clinical research experience. Previous experience in coordinating complex clinical trials. Prior experience working with pharmaceutical sponsors and CROs. Strong negotiation, multitasking and communication skills. Adaptable and able to coordinate and manage numerous simultaneous projects and meet strict deadlines. Knowledge of oncology medical terminology. ICH-GCP training and familiarity with clinical trial regulatory reporting requirements. Excellent computer skills and experience working with Microsoft Office programs. Able to work well in a team environment and able to complete individual assigned projects or tasks according to strict deadlines.
Preferred Qualifications: Clinical Trial experience (preferably in oncology or complex interventional trials). Society of Clinical Research Associates (SoCRA) or ACRP certification/membership. Oncology experience. Experience in study start up, Research Ethics Board and Health Canada applications, experience using clinical trial (electronic case report form) eCRF software, various databases or electronic medical records (e.g. Connect Care, Netcare). Knowledge of clinical trial regulatory framework.
