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Research Coordinator

2 months ago

Hamilton, Ontario, Canada Hamilton Health Sciences Full time

Job Summary

The Research Coordinator will provide support to the Research Coordinator to oversee the operation and management of research projects. This includes adhering to Good Clinical Practice and incorporating GCP requirements in all stages of research projects from start-up to close-out.

Key Responsibilities

  • Support the Research Coordinator in overseeing the operation and management of research projects.
  • Adhere to Good Clinical Practice and incorporate GCP requirements in all stages of research projects.
  • Adhere to regulatory and local requirements, including annual safety reports and periodic safety reports.
  • Adhere to timelines and milestones.
  • Provide support to all collaborators (sites/countries) on a regular basis through communication.
  • Liaise with internal and external collaborators involved with research projects to develop study agreements, complete regulatory/ethics submissions, and process payments for sites and other collaborators.
  • Compile, review, and file essential documents.
  • Help with training and orientation of study sites and staff.
  • Help develop Manual of Operations and other study support tools, reports, and trackers.
  • Help create and test data reports, databases, audit case report forms (CRFs), and related programs.
  • Help coordinate the process of transferring prepared study data to the study sponsor.
  • Respond to data-related questions and queries from internal and external partners.
  • Coordinate logistics, review requirements, and confirm accuracy for the shipping and collection of materials and supplies for the main study as well as for sub-studies.
  • Prepare for meetings and teleconferences.
  • Implement all study-related amendments requested by the Principal Investigator.
  • Respond to daily inquiries and facilitate communications on behalf of the central site.
  • Help with publications and other study-related documentations.
  • Perform activities related to major protocol deviations.
  • Creation of data collection forms.
  • Regular communication with external parties.
  • Help provide training to staff.
  • Help provide training to external study staff.
  • Attend regular meetings, prepare minutes, and lines of action.

Requirements

  • Bachelor's degree in a relevant field of study.
  • Requires 2 years of relevant experience.
  • Clinical Trial experience.
  • GCP, TCPS2 training.
  • Cardiology research experience.

Additional Information

As a condition of employment, you are required to submit proof of full COVID-19 vaccination to Employee Health Services.

Hamilton Health Sciences fosters a culture of patient and staff safety, whereby all employees are guided by our Mission, Vision, Values, and Values-Based Code of Conduct.

Hamilton Health Sciences is a teaching hospital and all staff and physicians are expected to support students and other learners.

To be considered for this opportunity, applicants must apply during the posting period. All internal and external applicants may ONLY apply via the Careers website.

Hamilton Health Sciences is an equal opportunity employer and we will accommodate any needs under the Canadian Charter of Rights and Freedom, Accessibility for Ontarians with Disabilities Act, and the Ontario Human Rights Code.