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

Clinical Trial Management, Good Clinical Practice, Regulatory Compliance, Data Management, Participant Interviewing, Sample Collection, Document Filing, Communication, Project Coordination, Report Generation

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 (sponsor/CRO/clinical team) on a regular basis through communication. Compile, review, and file essential documents Help develop Manual of Operations and other study support tools, reports, and trackers Conduct structured project participant interviews, support facilitating research related participant visits Prepare and maintain study materials related to central laboratory sample collection Ensure that the relevant research methodology is applied and all research material is handled in accordance with established protocols, policies, and procedures 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, and study worksheets applicable to the relevant study protocol Regular communication with internal and external parties Help provide training to staff Attend regular meetings prepare minutes and lines of actions Qualifications/Requirements: Bachelor's degree in a relevant field of study, or related experience equivalent. Requires 2 years of relevant clinical trial experience. GCP Certificate. Excellent oral and written communication skills. Assets Clinical Trial experience. GCP, TCPS2 training

How To Apply:

Incase you would like to apply to this job directly from the source, please click here

Responsibilities

Support the Research Coordinator in managing clinical research projects from startup to closeout while adhering to GCP and regulatory requirements. Responsibilities include coordinating participant visits, managing study materials, and handling data reports and communications with sponsors.