Clinical Research Coordinator - Ottawa, Canada - OHRI

OHRI

Verified Company

Ottawa, Canada

2 weeks ago

Posted by:

Sophia Lee

beBee Recruiter

Description

Dr. Cheung is also keenly interested in leveraging artificial intelligence to improve patient care.

Finally, our team works closely with patient and caregiver partners to ensure that research design, implementation and translation meet the needs of the ultimate beneficiaries of our research.

There will thus be an opportunity to work with a wide range of individuals from different scientific and community groups.

The prospective Research Coordinator will support Dr. Angela Cheung and the researchers and clinicians within the Centre for Liver of Eastern Ontario (CLEO). Activities will include coordinating prospective investigator-initiated studies as well as industry sponsored trials.

Expected Responsibilities:

Work under the general direction of the Senior Scientist to coordinate several investigator-initiated studies as well as industry sponsored trials.

Basic Requirements (Education/Experience):

Mandatory minimum of 3 years of experience in a clinical research environment and a postsecondary degree or diploma
Evidence of training certification in Tri-Council Policy Statement 2 (TCPS2), the International Conference on Harmonization
Good Clinical Practice Guidelines (ICH-GCP) and Health Canada Division
Previous experience managing investigatorinitiated, multicenter trials including communication with potential new sites, aiding new sites with study startup activities, conducting site initiation, and training visits and ensuring sites are conducting trial in accordance with protocol and governing regulations through regular site monitoring.
Experience drafting study protocols and study documents.
Experience submitting and managing REBs.
Experience managing large data sets, issuing queries and resolution.
Experience organizing and running Steering Committees, DSMB meetings and Adjudication Committee meetings.
Strong computer literacy and experience using Microsoft Word, Teams, Outlook, Excel, and PowerPoint software.
Great interpersonal skills and ability to communicate scientific research to study teams, patients and to the public (inperson and virtual)
Strong ability to work in a fastpaced environment, with excellent communication and organizational skills.
Able to work collaboratively and effectively as both part of an interdisciplinary team and independently.
Attention to detail to ensure the accuracy of data and protocol requirements.

Preferred Qualifications:

Proficiency in English and basic knowledge of French
Experience in clinical medicine and/or hepatology
Experience in running international, multicenter clinical research trials.
Experience submitting to Health Canada
Experience in project management
SOCRA CCRP Certified

Contract Details:

This is a 1-year full-time contract with the possibility of renewal.

This position is hybrid and requires 3 in person days weekly.

Salary:
Min: $ 32.964/hr - Max: $47.531/hr

Comments to Applicant:

Please submit a focused cover letter and curriculum vitae, in a single PDF using the naming convention "Last Name, First Name.

"

Contact Info:

Name:
Jennifer Brownrigg

Title:
Research Administrative Assistant

Program:
Clinical Epidemiology

Ottawa Hospital Research Institute

The Ottawa Hospital Research Institute is committed to building and sustaining a welcoming and supportive culture that promotes equity, diversity and inclusion for trainees, researchers, and staff. We are devoted to identifying and removing barriers that limit equitable access to opportunities within our organization. The Ottawa Hospital Research Institute strongly supports initiatives that encourage the participation of all groups, in particular the four groups defined in the Employment Equity Act (women, Indigenous peoples, persons with disabilities and members of visible minorities)._
We thank all applicants for their interest. However, only those invited for an interview will be contacted. The Ottawa Hospital Research Institute is an equalopportunity employer. Upon request, accommodations due to a disability are available throughout the selection process._