Research Coordinator

2 weeks ago

Edmonton, Canada University of Alberta Full time

**MED Critical Care Medicine**:

- Competition No.

**S100351041**
- Posting Date

**May 08, 2023**
- Closing Date

**May 22, 2023**
- Position Type

**Full Time - Grant Funded**
- Salary Range

**$51,055 to $69,342 per year**
- Grade

**08**
- Hours

**35**

This position is a part of the Non-Academic Staff Association (NASA).

This position has a term length of one year plus a day and offers a comprehensive benefits package which can be viewed on our Benefits Overview page.

**Location**

Work will primarily take place at North Campus Edmonton. This role is in-person.

**Working for the University of Alberta**

The University of Alberta acknowledges that we are located on Treaty 6 territory, and respects the histories, languages and cultures of First Nations, Métis, Inuit and all First Peoples of Canada, whose presence continues to enrich our vibrant community.

The University of Alberta is teeming with change makers, community builders, and world shapers who lead with purpose each and every day. We are home to more than 40,000 students in 200+ undergraduate and 500+ graduate programs, over 13,000 faculty and staff, 260,000 alumni worldwide and have been recognized as one of Canada’s Greenest Employers for over a decade.

Your work will have a meaningful influence on a fascinating cross section of people—from our students and stakeholders, to our renowned researchers and innovators who are quite literally curing diseases, making discoveries and generating solutions that make the world healthier, safer, stronger, and more just.

**Position**

The purpose of this position is to provide support to clinical research in the Department of Critical Care Medicine, ranging from in-house investigator research to industry sponsored research. Under the direction of the Senior Research Coordinator
- lead and the Principal investigator this position is diverse and complex, with some standard procedures and day-to-day research operations, procedures and protocols, as well as the development of new procedures and techniques, and independent problem solving. As this position is responsible for coordinating various Investigator initiated and industry sponsored research studies in the UAH General Systems Intensive Care Unit and the SCH Intensive Care Unit, work is done with an independent schedule and mínimal supervision. Driving between sites is required.

**Duties**
- Participates in protocol management: reviews and adheres to multiple research protocols
- Assists investigators with the preparation of documents for ethics submission (consents, protocols, study progress updates, adverse events reporting)
- Assembles study specific source documents and prepares study binders to ensure regulatory documentation is maintained to meet study requirements
- Conducts screening and recruitment of potential study participants; including obtaining consent, performs study specific assessments pre
- and post-operatively as required/appropriate
- Provides instruction/teaching to study participants regarding study participation, protocol requirements, follow
- up schedule, the use of data collection tools
- Conducts patient follow-up, data collection, case report form (CRF) completion, study monitoring, data query resolution; promotes patient's adherence to the study and monitors patient safety in relation to study protocols
- Provides ongoing written and oral reporting with the University Health Ethics Research Office (ARISE) and Northern Alberta Clinical Trials and Research Centre (NACTRC); investigators and industry sponsors
- Works with investigators to notify departments regarding study termination/compliance; ensures appropriate retention of study files/materials
- Conducts daily aspects of trials according to defined study protocols
- Works with investigators and lead study sites regarding study termination, compliance, ensures appropriate retention of study flies and materials
- Reports adverse events promptly and accurately as described by the research protocol
- Prepares for and assists with site visits by monitors once studies are closed out
- Data collection for quality improvement
- Ensure the GCP guidelines are followed

**Minimum Qualifications
- Post-secondary degree in Biological Science, Epidemiology, Health Sciences; equivalent combination of clinical research experience and education may be considered
- Minimum 2 -3 years experience with clinical trials
- Class 5 Drivers License
- Previous experience recruiting patients and research experience involving patients
- Must be comfortable entering the ICU

**Preferred Qualifications**
- Completion of NACTRAC research coordinator course considered an asset
- Completion of Society of Clinical Research Associate (SOCRA) certification considered an asset

**How to Apply**

**We thank all applicants for their interest; however, only those individuals selected for an interview will be contacted.

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