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Clinical Research Coordinator
1 week ago
The individual will be jointly responsible for the day-to-day operations of a large multi-centered research trial as well as possible involvement in several smaller projects.
For the clinical trial, the individual will be involved with patient follow up. Experience performing venipuncture is a mandatory requirement.In addition, collection of data and entry, as well as image uploading to a central site, working with technologists, and radiologists reporting on the study is required.
Basic Requirements (Education/Experience):
- Bachelor's degree in health sciences or related field. RN preferred.
- A minimum 3 years of previous clinical research experience and multicentre trial coordination
- Evidence of training certification in Tri-Council Policy Statement 2 (TCPS2) and the International Council on Harmonization
- Good Clinical Practice Guidelines (ICH-GCP)
- Evidence of training in Food and Drug Regulations, Division 5, and/or Device Regulations, as applicable
- Familiarity with requirements specific to investigatorinitiated trials
- Phlebotomy skills and experience handling lab samples
- Ability to work independently and as a team member.
- Ability to manage multiple projects at one time.
- Strong computer skills: MS Word, Outlook, and Excel
- Attention to detail to ensure accuracy of data and protocol requirements.
- Possess strong leadership, organizational, time management, problemsolving, and interpersonal skills.
- Effective decision making, organizational and communication skills.
- Demonstrate meticulous attention to detail and knowledge of good documentation practices in clinical research.
- Highly motivated to initiate and complete tasks independently
- Demonstrate flexibility in adapting to changing priorities/workloads and maintain strict confidentiality.
Preferred Qualifications:
- Bilingualism
- Certified Clinical Research Professional is an asset (ACRP OR SOCRA)
Contract Details:
This is a 2-year full-time 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:
Contact Info:
Name:
Dr. Betty Anne Schwarz
Title:
Senior Clinical Research Program Manager
Program:
Department of Medical Imaging
Ottawa Hospital Research Institute
Address: 751 Parkdale Avenue, Suite 50- 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.
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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