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Job Location | Toronto, ON |
Education | Not Mentioned |
Salary | Not Disclosed |
Industry | Not Mentioned |
Functional Area | Not Mentioned |
Job Type | Full Time |
Research Coordinator IThe Department of Obstetrics and Gynaecology works under a centralized research program. At any given time, the dept. has 60-70 active studies running. The research team is responsible to provide support to the PIs and studies. We initiate, coordinate studies including clinical trials. We are the primary point of communication for the REB and internal and external study related queries. The research team is also responsible to make sure that the studies are approved by the REB.The Department of Obstetrics and Gynaecology is currently looking for a Research Coordinator I. This position performs research activities involving project design, collecting, summarizing or analyzing data. Tasks may include but not limited preparing and submitting new study documents to REB ,updating information of existing studies with REB, adhering to research protocol andstudy coordination by carrying out various aspects of conducting a clinical trial, creating case report forms, data extraction and data entry.Duties & Responsibilities:Be the proary source of communication regarding REB and study related queries from PIs,General office duties e.g. filing, faxing, mailings, courier services, photocopying, etc.Collection, transcription and entry of study related dataLimited processing of dataConducting literature searchesInteracting with various departments such as pharmacy, laboratories, medical records, etc.Present research related information, including written study reports when necessaryRepresent St. Michael’s Hospital at protocol development and study initiation meetingsDesign of all source documents, patient education materials, etc.Coordinating studies including ongoing laboratory, pharmacy, etc. activities pertaining to studyAssisting Investigators in the interpretation and implementation of study protocolsAssisting Investigators in the initiation of new researchInteracting with sponsoring agencies regarding requests for clarifications of data and/or assisting monitors during site visitsCollecting data via phone calls, interviewsScreening data for study inclusion according to protocolQualifications:Minimum of Bachelor’s degree in health science field, however Masters preferredExperience in new study submissionExcellent attention to detail and proven ability to learn new skills.Superior organizational skills to manage multiple projects in a timely manner and flexibility to adapt to changing workload.Professionalism and self-motivationGood personal and program time/detail management skillsAble to work independently and as part of a teamAs applicable, knowledge of anatomy, physiology, pharmacology, GCP (HPB, FDA) regulation and guidelines, laboratory and diagnostic testing, health record analysis,Excellent computer skills including Word Perfect, Word, Excel, Powerpoint, Internet, database and statistical softwareAs a condition of employment, all external hires will be required to submit proof of COVID-19 vaccination or documentation unless a valid accommodation under the Ontario Human Rights Code exists. All internal candidates must be in compliance with Unity Health Torontos COVID-19 Vaccination Policy.Quick Apply