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Research Assistant

Hamilton, ON
  • Number of positions available : 1

  • 27.19 to 34.86 $ according to experience
  • Full time
  • Starting date : 1 position to fill as soon as possible

• Support Research Coordinator to oversee the operation and management of research projects.
• Adhere to Good Clinical Practice and incorporate GCP requirements in all stages of research projects from start up to close up. 
• Adhere to regulatory and local requirements (i.e. annual safety reports, 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 query 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 actions.


Qualifications

Qualifications:

  • Bachelor's degree in a relevant field of study.
  • Requires 2 years of relevant experience. 

Assets:

  • Clinical Trial experience
  • GCP, TCPS2 training 

Requirements

Level of education

undetermined

Work experience (years)

undetermined

Written languages

undetermined

Spoken languages

undetermined