Clinical Research Coordinator - Ottawa, Canada - OHRI

OHRI

Verified Company

Ottawa, Canada

3 weeks ago

Posted by:

Sophia Lee

beBee Recruiter

Description

technology enhanced (like virtual reality) simulation/medical education and hyperbaric medicine.

Our program relies on a variety of research methods:
qualitative, quantitative and knowledge synthesis

Tasks may include:

Project coordination, including organizational and logístical aspects of studies as well as reporting to granting agencies and arranging funds transfers
Bookkeeping for project cost centers and salary accounts
Assisting with study protocol development and manuscript preparation
Data management and database maintenance for various projects, including Health Canada regulated clinical trials
Quantitative and qualitative data collection and analysis
Upkeep of regulatory documents for health Canada regulated trials
Set up and participate in the training requirements for staff and trainees
Participation in the development and delivery of presentations to internal and external groups

Basic Requirements (Education/Experience):

Education

Graduate degree, in a healthrelated discipline, such as Psychology, Sociology, Epidemiology or Public Health (Master's degree or PhD)
Training in quantitative analysis preferred.
Evidence of training certification in Tri-Council Policy Statement 2 (TCPS2) and the International Council on Harmonisation
Good Clinical Practice Guidelines (ICH-GCP)
Evidence of training in Food and Drug Regulations, Division 5, and/or Device Regulations, as applicable
Previous training/experience as a healthcare professional is considered an asset.

Employment Experience

3 years' experience in a healthrelated research environment.
Demonstrated experience recruiting, screening and enrolling participants into research studies.
Knowledge relevant to the research process, including obtaining informed consent, data collection, data analysis, and manuscript preparation.
Experience coordinating investigatorinitiated multicentre research trials is considered an asset.
Previous experience of healthCanada regulated trials will be considered as an asset

Personal Qualities

Flexible and cooperative spirit with a strong commitment to team efforts.
Outcomedriven selfstarter with the ability to work independently.
Selfdirected learning abilities.
Excellent organizational, prioritization, and timemanagement skills required to coordinate multiple activities to meet tight or changing deadlines.
Attention to detail to ensure accuracy of data and protocol requirements
Strong problemsolving and decisionmaking skills required to deal with unexpected

- situations or issues.

Excellent interpersonal and communication skills (written and oral).
Commitment to quality, excellence, and principles of equity, diversity, and inclusion.

Preferred Qualifications:

Excellent computer skills (MS Word, SharePoint, Excel, PowerPoint and Outlook).
Comfort working remotely and virtually, including using videoconference platforms (e.g., Zoom, Microsoft Teams).
Proficiency with qualitative (e.g., NVivo) and/or quantitative (e.g., SPSS) analysis and systematic review (e.g., Covidence) software is an asset.
Experience in research coordination
Bilingualism (French/English) is considered an asset.
Experience working within OHRI or the University of Ottawa

Contract Details:

This is a 1year fulltime contract with the possibility of renewal

Salary:

Min:
$32.004/hr - Max:$46.

147/hr
Comments to Applicant:

Please send:

A complete CV with description of research experience, AND

Contact Info:

Name:
Drs. Gu and Boet

Title:
Principal Investigators

Program:
Clinical Epidemiology

Ottawa Hospital Research Institute
Address: 1053 Carling Ave, Ottawa Ontario, K1Y 4E9

We thank all applicants for their interest. However, only those invited for an interview will be contacted. The Ottawa Hospital Research Institute is an equal-opportunity employer. Upon request, accommodations due to a disability are available throughout the selection process.