Research I

3 weeks ago

Edmonton, Canada Alberta Health Services Full time

Your Opportunity:

The Clinical Trial Unit is a specialty area at the UAH where clinical researchers design, conduct, analyse and publish clinical trials and other health studies. 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 a Research I to provide support for industry funded clinical research trials. You will work in a variety of clinical therapeutic areas at the University of Alberta. The main responsibilities of this position includes , obtaining informed consent, pre-screening, screening and randomizing of eligible participants, follow-up visits, reporting/ documenting of adverse events and serious adverse events, performing study related activities as per the protocol, collecting and reporting clinical trial data, and completing/maintaining regulatory documents as required. As a Research I, you will require exceptional organizational skills that are necessary to ensure trial information is timely, accurate, valid and to the sponsor's satisfaction. A main component of this role is to ensure studies are run according to the protocol and Health Canada regulations. Working under limited supervision, you will perform diversified duties requiring independent judgement and confidentiality. To be successful in this role, you will require excellent critical and problem-solving skills and the ability to work in a team environment. You must be able to handle multiple demands with short timelines while remaining sufficiently flexible to accept new workload as necessary.

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.

Required Qualifications:

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

Additional Required Qualifications: Preferred Qualifications:

Connect Care Research Training.Experience with ARISE applications and processes. Knowledge of medical terminology.Phlebotomy experience.

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