Research Assistant at Hamilton Health Sciences Corporation

Hamilton, Ontario, Canada -

Full Time

Start Date

Immediate

Expiry Date

21 Sep, 26

Salary

0.0

Posted On

23 Jun, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Good Clinical Practice, Project Management, Regulatory Submissions, Data Management, Clinical Trial Coordination, Microsoft Office Suite, REDCap, Communication Skills, Time Management, Teamwork, Medical Chart Review, Participant Enrollment

Industry

Hospitals and Health Care

Description

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 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 Attend regular meetings prepare minutes and lines of actions. Other working conditions may involve field work and irregular hours, such as weekend and evening work. Enrolling participants via telephone, completing and tracking follow-up, medical chart reviews, and ongoing communication with project teams. Bachelor's degree in a relevant field of study. Requires 2 years of relevant experience. Proficient working knowledge of the Microsoft Office Suite and research-specific databases, specifically Word, Excel, and REDCap. Full working knowledge of safety regulations and government legislation is an asset Excellent written and oral communication skills Ability to manage time and determine priorities Effective project management, personal initiative and teamwork necessary Assets Clinical Trial experience. GCP, TCPS2 training

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Responsibilities

Support the Research Coordinator in managing research projects, ensuring adherence to GCP and regulatory requirements. Coordinate logistics, manage study documentation, and liaise with internal and external collaborators to ensure project milestones are met.