Clinical Research Coordinator
2 days ago
**Tasks may include**:
- Patient recruitment and follow-up, data collection, and data entry
- Overseeing study start-up activities (approvals, contract, regulatory documents, training) internally for investigator-initiated trials
- Maintaining current up-to-date regulatory binder/files
- Facilitating physician oversight over study participants following GCP requirements
**Basic Requirements (Education/Experience)**:
- Bachelor’s degree in a health science-related field or equivalent
- Three (3) years’ experience coordinating clinical trials
- A comprehensive understanding of the clinical research process from study start-up to completion
- Experience coordinating investigator-initiated multi-center research trials
- Evidence of training certification in Tri-Council Policy Statement -2 (TCPS-2) 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
- Clinical research certification (ACRP or SOCRA)
- 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**:
- Knowledge of EPIC and TOH processes for arranging diagnostic imaging, investigational therapy, and patient follow-up visits
- Experience in clinical hematology
- Bilingualism is considered an asset
**Contract Details**:
This is a full-time 1-year contract position with the possibility of renewal, located at the General Campus of The Ottawa Hospital
**Salary**: Min: $31.687/hr. Max: $45.690/hr.
Comments to Applicant:
Please send a resume to:
**Contact Info**:
Name: Amanda Pecarskie
Title: Senior Research Program Manager
Program: Clinical Epidemiology
Ottawa Hospital Research Institute
Address: 501 Smyth Rd, Ottawa, ON K1H 8L6
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.
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