Clinical Research Coordinator - Ottawa, Canada - OHRI
Description
Tasks may include:
- Patient recruitment and followup, data collection, and data entry
- Overseeing study startup activities (approvals, contract, regulatory documents, training) internally for industrysponsored or investigatorinitiated trials
- Maintaining current uptodate regulatory binder/files
- Facilitating physician oversight over study participants following GCP requirements
Basic Requirements (Education/Experience):
- Bachelor's degree in a health sciencerelated field or equivalent
- Three (3) years' experience coordinating clinical trials
- A comprehensive understanding of the clinical research process from study startup to completion
- Experience coordinating industrysponsored malignant hematology research trials
- Evidence of training certification in Tri-Council Policy Statement 2 (TCPS2) and the International Conference on Harmonization
- Good Clinical Practice Guidelines (ICH-GCP)
- Evidence of training in Food and Drug Regulations, Division 5, and/or Device Regulations, as applicable
- Knowledge and recent evidence of training in clinical research standards
- Ability to build and maintain internal and external professional relationships with patients, colleagues, and the multidisciplinary team
- Proven ability to work independently and navigate competing priorities
- Demonstrates initiative and resourcefulness in the development, implementation of projects, and ability to evaluate progress, action areas of improvement
- Commitment to quality and excellence, attention to detail in ensuring compliance with the protocol
- Effective communication skills (written and oral)
- Strong computer and data entry skills: including experience with electronic data capture
- Experience in arranging monitoring activities with the sponsor
Preferred Qualifications:
- Clinical research certification (ACRP or SOCRA)
- Knowledge of EPIC and TOH processes for arranging diagnostic imaging, investigational therapy, and patient followup visits
- Experience in clinical hematology
- Bilingualism is considered an asset
Contract Details:
This is a 1-year full-time contract with the possibility of renewal
Salary:
Min:$32.004/hr - Max:$46.147/hr
Comments to Applicant:
Please send a cover letter outlining your experience in relation to this job posting and your resume to
Contact Info:
Name:
Amanda Pecarckie
Title:
Research Program Manager
Program:
Clinical Epidemiology
Ottawa Hospital Research Institute
Address:
General Campus
- 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._
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