Research I

14 hours ago

St Albert Alberta TN, Calgary, Canada Alberta Health Services Full time

The Clinical Trial Unit supports the Principal Investigators in conducting research studies at AHS/UofA and within the Edmonton zone. Embedding research, innovation and analytic capacity in the healthcare system helps ensure AHS provides patient-focused, quality healthcare to more than four million Albertans. Come be part of exciting leading-edge research and join our team of professionals in the Clinical Trial Unit (CTU). The Clinical Trials Unit is recruiting for a Research Coordinator to provide support for clinical trials and research for the Western Hand & Upper Limb Facility (WULF) at the Sturgeon hospital in St. Albert. The WULF is a specialized upper extremity centre providing care to patients with upper extremity conditions. WULF has a busy and dynamic research program focused on conducting high-quality research projects that have meaningful impacts on the care delivery and outcomes of our patients with various upper extremity conditions. The main responsibilities of this position include: ARISE applications, operational and administrative approval before recruitment commences, screening and consenting of eligible participants, collection and documentation of research data, completing/maintaining regulatory documents as required by the protocols. As a Research Coordinator, you will require exceptional organizational skills that are necessary to manage multiple studies and ensure that study/trial information is timely, accurate, valid according to the study protocol and sponsor and Health Canada regulations, when applicable.

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.

Diploma or degree in a health or science related field. Registration with applicable professional association or college where required.

2-3 years clinical trial research experience. Current experience in consenting and enrolling participants in clinical trials. Current experience in Musculoskeletal assessment skills. Connect Care research training, current experience with REDCap Data Capture and other databases, ARISE applications including creating informed consents, amendments, renewals and closeouts, operational approvals, administrative approvals and AHS processes. Knowledge of medical terminology is essential. Knowledge of clinical trial regulations and guidelines (ICH-GCP training, Health Canada and FDA). Ability to handle multiple demands with short timelines while remaining sufficiently flexible to accept new workload as neccessary. Strong interpersonal and communication skills to effectively manage and communicate with participants on the studies. Demontrated excellent problem solving skills and the ability to work in a team environment. It is vital that you demonstrate the insight of when to escalate/report participants clinical concerns to Nursing staff and/or Investigator. As a Research Coordinator, you shall harness professionalism and strong interpersonal skills to effectively manage and communicate with participants on the studies. It is vital that you demonstrate the insight of when to escalate/report participants clinical concerns to Nursing staff and/or Investigator.

As required.

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