Research Coordinator Cheo Ri
2 months ago
Compensation Pay Range:
$0.00-$0.00
Summary:
Please send your resume with a cover letter to Brenda Bradley at
Posting # - RI-24-044
Posting Period - October 18 to November 1, 2024
POSITION: Research Coordinator
Endocrinology
TERM: Full-time (1.0 FTE) 1 year contract, with possibility of renewal
SALARY: $35.00/hr - $42.00/hr, will commensurate will skills and experience
REPORTS TO: Dr. Karine Khatchadourian
Children’s Hospital of Eastern Ontario Research Institute (“CHEO RI”) is the research arm of the Children’s Hospital of Eastern Ontario - Ottawa Children’s Treatment Centre (“CHEO”) and an affiliated institute of the University of Ottawa. We acknowledge that Ottawa is built on un-ceded Algonquin Anishinabek territory. The Algonquin Anishinabek Nation have lived on this territory for millennia and we honour them and this land. Their culture and presence have nurtured and continue to nurture this land. CHEO RI also honours all First Nations, Inuit and Métis peoples and their valuable past and present contributions to this land. CHEO is a beloved institution and workplace that is widely recognized for being an anchor in our community. CHEO RI works to create new knowledge and evidence to support CHEO in its provision of world-class care to our children. Our mission at CHEORI is to connect exceptional talent and technology in pursuit of life-changing research for every child, youth and family in our community and beyond.
CHEO RI has an immediate requirement for a Research Coordinator.
Under general supervision, the Research Coordinator provides assistance with diverse clinical research projects related to Endocrinology, including regulated treatment trials (project scheduling, REB submissions and renewals, database management, data entry, patient visit scheduling, invoicing). The Research Coordinator will be responsible for coordinating clinical trials of cutting-edge therapies.
MAIN RESPONSIBILITIES
Under the general supervision of the Dr. Karine Khatchadourian (Endocrinology), the Research Coordinator will:
- Liaise with research team staff, clinicians, patients, families and clinical collaborators
- Ensure efficient day-to-day operation of research data collection protocols and data analysis activities
- Prepare submissions to the REB including consent/assent form and research protocols development
- Be responsible for patient recruitment, including screening and obtaining informed consent/assent
- Be responsible for administering standardized clinical assessments
- Be responsible for the collection and scoring of research information in REDCap
- Track patient progress and coordinate follow-ups
- Ensure data entry of all measures and surveys are done in a timely manner, as well as quality control
- Monitor budget and invoice for study-related expenses
- Negotiate study budgets and prepare contract submissions
- Supervision of research staff (research assistants and medical students)
- Assist with grants, report writing, preparing presentations, posters and publications
- Notify affiliated physicians of any clinical therapy or study protocol concerns
- Organize and facilitate meetings associated with research activities
- Perform other duties as assigned or directed to meet the goals and objectives of the research team
- Responsible for the execution of clinical research studies and programs
- Collect, process, and assist in the compilation and verification of research data, samples, and/or specimens (following strict protocol and detailed instructions)
- Enter data forms and documents into databases and other systems (eCRF)
- Assist with routine data verification and quality control, ensuring data integrity and consistency with study protocol
- Provide overall administrative assistance to the research team
- Invoicing for study-related expenses
QUALIFICATIONS, SKILL AND ABILITIES
- Bachelor’s degree in related field (Essential)
- Minimum 2 years experience as a Clinical Research Coordinator (Essential)
- Minimum 1 year experience working on regulated clinical trials (preferred)
- GCP, ICH, Health Canada Division 5 certifications (Essential)
- Understanding of research design, guidelines and standards governing clinical research (Essential)
- Understanding of the Personal Health Information Protection Act (Essential)
- Excellent computer skills, including advanced knowledge of research related software (Excel, PowerPoint, Outlook, REDCap, literature search engines, Reference Manager or equivalent) (Essential)
- Experience in report writing, publication and communication briefs (preferred)
- Outstanding organizational, accountability and time management skills (Essential)
- Ability to work independently with mínimal supervision and think critically (Essential)
- Ability to work effectively in a multidisciplinary team environment (Essential)
- Excellent written and verbal communication skills (Essential)
- Excellent inter-personnel skills (Essential)
- Bilingualism (English/F
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