Research Assistant/Study Coordinator - Jobs in Edmonton, AB

Job Description

MED Medicine DepartmentCompetition No. - S104648972Posting Date - Nov 08, 2022Closing Date - Nov 15, 2022Position Type - Full Time - Grant FundedSalary Range - $46,627 to $62,954 per yearGrade - 07Hours - 35This position is a part of the Non-Academic Staff Association (NASA).This position has a term length of 1 year plus 1 day and offers a comprehensive benefits package which can be viewed on our Benefits Overview page.Working for the University of AlbertaThe 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.PositionUnder the direction of the Principal Investigator (Pl), Dr. Penelope Smyth, the Research Assistant/Study Coordinator (RA/SC) will participate in the general research operations of clinical trials which focuses on MS disease. The incumbent will assist in coordinating observational cohort and intervention studies of participants. Current studies include: Canadian Prospective Cohort Study to Understand Progression in Multiple Sclerosis (CanProCo) and Tomorrow MS: The Alberta Extended Cohort. The incumbent will assist in recruitment, assessment, data collection and management. The incumbent will also manage scheduling of study participants.In this position, the Research Assistant/Study Coordinator must be able to work independently to organize and perform the day-to-day operations of the research studies. This may include but is not limited to: recruiting and consenting subjects; coordinating subject research visits; collecting data via questionnaires, cognitive assessments, and other data-gathering processes as required; recording data in local and shared databases; drafting ethics applications and providing ongoing written and oral communication with the Research Ethics Board, NACTRC. Collection of blood samples - training can be provided and transferring of MRI data.Duties

• Self monitor and self-audit responsibilities
• Screen, recruit (face-to-face, telephone, e-mail), and enroll research participants.
• Coordinate protocol related research procedures, study visits.
• Ensure the smooth and efficient day-to-day operation of research and data collection activities including assisting the Pl
• Administers cognitive tests, study questionnaires, and other data-gathering processes as per project protocol
• Act as a liaison for participants, investigator, REB, sponsor, and healthcare professionals
• Educate participants and family on protocol
• Responsible for all data backup and entry in paper and electronic form, in local and electronic databases and work with data-management center to assure that data is uploaded, accessible, accurate, and available for analysis
• Phlebotomy
• Manage the transfer of MRI data to sponsor
• Facilitate study close out activities
• Retain records/archive documents after study close out
• Understand good clinical practice and regulatory compliance
• Comply with institution policies, standard operating procedures, and guidelines

Minimum Qualifications

• Bachelor of Science or equivalent in a related field
• Project administration or related experience in, managing data and patient assessment
• A clear understanding of the sponsors responsibilities under ICH/GCP requirements and experience in applying ICH/GCP guidelines, research ethics policies and Tri-Council policies for research involving humans
• Knowledge of Albertas health system and Canadas health research environment (including the submission of ethics applications and related AHS research agreement process)
• Experience in clinical research and/or knowledge translation
• Experience with working with online data-entry platforms (e.g., LORIS, REDCap, etc.)
• Strong written and verbal communication, interpersonal, teamwork and organizational skills
• Strong computer skills (MS Office, SPSS, Google Drive, LORIS, REDCap, NAC T RC. ARISE, etc.)
• Training in research study coordination (e.g., CITI Clinical Research Coordinator Course, NEW DIRECTIONS Coordinator Training Program, etc.)

How to ApplyNote: Online applications are accepted until midnight Mountain Standard Time of the closing date.We thank all applicants for their interest; however, only those individuals selected for an interview will be contacted.The University of Alberta is committed to an equitable, diverse, and inclusive workforce. We welcome applications from all qualified persons. We encourage women; First Nations, Métis and Inuit persons; members of visible minority groups; persons with disabilities; persons of any sexual orientation or gender identity and expression; and all those who may contribute to the further diversification of ideas and the University to apply.Quick Apply

• Terms & Conditions
• New Privacy
• Privacy Center
• Accessibility

For Job Seekers

• Browse Jobs
• Advanced Job Search
• Emplois Quebec

For Employers

• Post a Job
• SimplyHired OnDemand

Stay Connected