OverviewCHEO RESEARCH COORDINATOR Full Time in Ontario
Branch ON CA
§ May be responsible for patient recruitment including screening and obtaining informed consents. Research including Personal Health Information Protection Act…
The Research Coordinator coordinates one or more studies/clinical trial or a large multi-site trial for one or more Principal Investigators. This would include administration of the study/clinical trial, management of data collection, budgetary monitoring and training and supervision of study personnel.
MAIN RESPONSIBILITIES (This is not an exhaustive list)
§ Responsible for the administration of the study or clinical trial.
§ May be responsible for patient recruitment including screening and obtaining informed consents.
§ Responsible for the creation of data forms and study procedure manuals.
§ Acts as key communicator between study personnel, sites and investigators.
§ Responsible for supervision of the collection, scoring, and coding of research information.
§ Will assist in the grants manship process including REB submissions.
§ Perform basic statistics and prepare summary data results.
§ Contribute to the preparation of manuscripts.
§ Training and supervision of study personnel.
§ Budgetary monitoring.
§ Coordinate, organize and chair relevant research meetings.
§ Perform work in accordance with the provisions of the Occupational Health and Safety Act and Regulations and all CHEO corporate/departmental policies and procedures related to Occupational Health and Safety.
§ Perform other related duties as assigned by supervisor.
§ Police Record Check (PRC) (Essential)
§ Current Certification of Registration with the College of Nurses of Ontario (Essential)
§ University undergraduate degree (BScN, B.A, BSc.) (preferredl)
§ Minimum 1 years research experience (Essential)
§ Understanding of research design, procedures, guidelines and standards governing clinical
research including Personal Health Information Protection Act (Essential)
§ Experience with Health Canada procedures, Good Clinical Practice Guidelines (Preferred)
§ Experience with clinical trials registration (Preferred)
§ Demonstrated management and organizational skills (Essential)
§ Data management experience (Essential)
§ Proficiency in computer skills (Microsoft Office) (Essential)
§ Strong Analytical skills (Essential)
§ Excellent communication (verbal and written), interpersonal and organizational skills (Essential)
§ Bilingual (French and English) (Preferred)
· Able to work in a dynamic, often hectic environment and be able to multi-task
· Able to be flexible with working hours in order to meet deadlines
· Able to work under tight deadlines
· Able to work in a team as well as independently under sometimes minimal supervision
Interested candidates should submit a cover letter of interest and curriculum vitae to [email protected] .
Should the applicant require any accommodations during the application process please notify CHEO RI Human Resources as per the Accessibility for Ontarians with Disabilities Act.
We thank all applicants for their interest. However, only those invited for an interview will be contacted.
Employment Type: Full Time
Location: Ontario, CA, US
Posted on: 2016-10-31