Research Coordinator

3 weeks ago


Toronto, Canada Women’s College Hospital Full time

Research Coordinator - Violence and Health ResearchWomen's College Hospital, 76 Grenville Street, Toronto, Ontario, CanadaJob DescriptionWomen's College Hospital (WCH) is an academic, ambulatory care hospital in Ontario with a focus on health for women, health equity and health system solutions. If you're ready to be part of a team that is revolutionizing the future of healthcare, then you will want to join an institution where the possibilities for innovation, new discovery and system thinking are limitless. Women's College Hospital is committed to equity, quality and patient safety as key professional values and essential components of daily practice. Healthcare Revolutionized 2030 is our roadmap to the future. Our strategy is built on the pledge that the founders of our hospital made 140 years ago and reaffirms our commitment to providing equitable, accessible, best-in-class healthcare for everyone – meeting people where they are on their healthcare journey and partnering with them to reach their goals of living their healthiest lives possible. The stage has been set for Women’s to accelerate our priorities and capture the momentum to catapult our system forward to revolutionize healthcare for everyone.Applicants must reside and be legally eligible to work in Ontario.This is a Temporary Full-Time opportunity.Type: ReplacementDuration: 12 monthsAn exciting opportunity for a Research Coordinator I exists with the ASTER (Addressing Sex Trafficking through Education and Research) program of research led by Dr. Janice Du Mont. The individual in this role will support the team members and activities associated with the research program.Summary of Duties, but not limited to:Assists with enhancing relationships among existing stakeholders and helps with the development of new partnershipsMonitors the progress and deadlines of research activities, develops and maintains records of research activities, and establishes and maintains operating policies and proceduresCoordinates the day-to-day activities of any staff specifically engaged in the carrying out of research for one or more projects within the research program, as appropriate to their positionPrepares periodic and ad hoc reports, as required by investigators, administrators, funding agencies, and/or regulatory bodiesActs as the primary administrative point of contact for internal research staff and as the primary operational liaison for internal and external collaborators working with the unit (e.g. other research organizations, funding agencies, regulating bodies, etc.)Proactively identifies barriers/threats/risks for project completion and work with team members including Investigators and Research Assistants to develop solutionsResponsible for collaborating with the Investigators and other relevant partners involved in the project both internally and externallyPlans, implements and coordinates all aspects of data collection and source documentation as per the organization’s policy and ICH/GCP guidelinesAids in ensuring the accuracy and integrity of data and investigating missing dataMay be responsible for processing data including statistical analysis, applying theoretical frameworks in accordance with study protocolPrepares, submits, and maintains Research Ethics Board (REB) applications both internally as well as submissions to external organizations (if applicable), tracks ethics approvals, and completes renewals/amendments as neededAssists in drafting related grant application documentsCollaborates with Investigator and/or team members to write and edit presentations, reports, budgets, proposals, publications, conference materials, and manuscripts.Assists with knowledge translation activities (e.g., drafting manuscripts, presentations, infographics, curricula, training tools)Maintains and updates ASTER WebPortal as requiredPlans and coordinates regular meetings for working groups, steering committees, and advisory boardsPerforms aspects of research protocol, as required, in accordance with specified program objectives. (e.g. participant recruitment, data collection, preparing data for analyses, etc.)As a role model and champion, you will work to identify and integrate safe, best practices into daily activities to foster the delivery of safe and exemplary care.The responsibilities described above are representative and are not to be construed as all-inclusive.QualificationsUndergraduate degree in healthcare or social sciences related field, Master’s degree preferredKnowledge of and/or experience working in the field of gender-based violence; knowledge of sex trafficking preferredMinimum three years of progressive experience working in a research environment and/or academic hospitalExcellent verbal and written communications skills, bilingualism an assetWork efficiently under pressure with strong judgement with excellent problem-solving skills and decision-making skillsKnowledge of planning and management processes for research (e.g., experience with the ethics approval process, federal granting agency guidelines, etc.)Familiarity with “Squarespace” an assetDemonstrated ability to take initiative and lead a wide variety of people at different levelsAbility to work independently with a high degree of initiative, discretion and tactExcellent interpersonal, verbal, and written communication skills are essentialAbility to maintain confidentialityComputer competency including familiarity with databases (REDCap, MS Access), EndNote, MS Word, MS Excel, and MS PublisherDemonstrated record of good performance and acceptable attendance will be considered as part of the selection criteriaProfessional behaviour and communication that meets the standards of the professional regulatory college or association, as applicable, and the standards of Women’s College HospitalThis position plays a critical role in acting as an advocate for safety and will demonstrate principles, practices and processes that will optimize a safe environment for allWhy Choose Us?Be part of a dedicated team committed to excellence.Shape the future of healthcare in a supportive environment.Enjoy competitive benefits and an excellent defined benefit pension plan (HOOPP).Women's College Hospital is a fully affiliated teaching hospital of the University of Toronto and is committed to fairness and equity in employment and our recruitment and selection practices. We encourage applications from Indigenous peoples, people with disabilities, members of sexual minority groups, members of racialized groups, women and any others who may contribute to the further diversification of our Hospital community. Accommodation will be provided in all parts of the hiring process as required under our Access for People with Disabilities policy. Applicants need to make their requirements known in advance.Women's College Hospital, 76 Grenville Street, Toronto, Ontario, Canada #J-18808-Ljbffr



  • Toronto, Canada Centricity Research Full time

    Position Title: Clinical Research Coordinator I (CRCI) Department: Clinical Operations Reports To: Operations Manager, Assistant Operations Manager Direct Reports: N/A POSITION FUNCTION The Clinical Research Coordinator I (CRC I) perform a variety of administrative and clinical activities to assist the Investigators in conducting clinical studies. The...


  • Toronto, Canada Headlands Research Full time

    Overview: **The Role** Toronto Memory Program is looking for a Clinical Research Coordinator to manage clinical research protocols. This individual will work directly with the investigators, and other research staff to ensure protocol visits are being conducted according to ICH GCP guidelines. **This Clinical Research Coordinator role will be based in...


  • Toronto, Canada Headlands Research Full time

    **Overview**: **The Role** Toronto Memory Program is looking for a Clinical Research Coordinator to manage clinical research protocols. This individual will work directly with the investigators, and other research staff to ensure protocol visits are being conducted according to ICH GCP guidelines. **This Clinical Research Coordinator role will be based in...


  • Toronto, Canada Clinical Research Full time

    Responsibilities: - Coordinate and oversee clinical research studies from start to finish - Collect and record data accurately and efficiently - Analyze research data and prepare reports for review - Ensure compliance with study protocols, regulations, and ethical guidelines - Collaborate with healthcare professionals, researchers, and study participants -...


  • Toronto, Canada Centricity Research Full time

    LMC Manna Research, IACT Health, and True North Clinical Research have united to become the largest network of fully-owned and integrated clinical research sites in North America, Centricity Research. The sites that were formerly known as LMC Manna bring phase I-IV clinical trial services with specialized focuses on endocrine disorders, real world evidence...


  • Toronto, Ontario, Canada Centricity Research Full time US$60,000 - US$90,000 per year

    Join Us at Centricity ResearchCentricity Research is one of the largest clinical research networks in North America. We are a fully centralized Integrated Research Organization (IRO) specializing in conducting Phase I-IV clinical trials in over 35 therapeutic areas: inpatient and outpatient; pharmaceutical, biotechnology, and medical device trials.About The...


  • Toronto, Canada Think Research Full time

    . ***ONSITE ROLE** **The Company** BioPharma Services Inc. is a subsidiary of Think Research. BioPharma Services was founded by two surgeons dedicated to advancing medical science to improve the life and spirit of their patients. With this same dedication and vision in mind, these physicians brought life to BioPharma. Through each success, and even some...


  • Toronto, Canada Psychedelic Research Consultants Inc. Full time

    Clinical Research Coordinator Psychedelic Research Consultants is a Canadian based consulting firm dedicated to the advancement of psychedelic science and therapeutics. We are looking for an experienced full-time Toronto based Clinical Research Coordinator (CRC) to work directly with the Principle Investigator (PI) and Research Director on assigned...

  • Research Assistant

    1 week ago


    Toronto, Canada Centricity Research Full time

    LMC Manna Research, IACT Health, and True North Clinical Research have united to become the largest network of fully-owned and integrated clinical research sites in North America, Centricity Research. The sites that were formerly known as LMC Manna bring phase I-IV clinical trial services with specialized focuses on endocrine disorders, real world evidence...

  • Research Assistant

    1 week ago


    Toronto, Canada Centricity Research Full time

    LMC Manna Research, IACT Health, and True North Clinical Research have united to become the largest network of fully-owned and integrated clinical research sites in North America, Centricity Research. The sites that were formerly known as LMC Manna bring phase I-IV clinical trial services with specialized focuses on endocrine disorders, real world evidence...