Job Description

The Research Coordinator\xe2\x80\x99s purpose is to help lead a team in the conduct of one or more research studies. The Research Coordinator is accountable to the Principal Investigator (PI) and or Senior Research Coordinator and is responsible for all aspects of research projects highlighted below.

• Identify and recruit study participants including informed consent process, randomization and implementation of study protocol procedures.
• Completion of participant assessments
• Review of Quality Control Reports and resolution of queries.
• Serious adverse event reporting.
• Schedule follow up with study participants as per study protocol.
• Act as a contact for internal support departments and external stakeholders.
• Participate in the education of front line health care staff re: study protocol and procedures
• Assist with the development and monitoring of study timelines.
• Provide coordination and direction or support the development of data management methodologies for multiple studies; including key data management methods.
• Provide coordination and direction or support in the development of site management practices for multiple studies; including data collection, cleaning and analysis and maintenance of essential site documentation per ICH-GCP guidelines, management and preparation of regulatory and health authority documentation, research ethics board documents and study contact information.
• Engage in ongoing communication and coordinate regular meetings with supervisor and key study specific stakeholders.
• Prepare presentations for external and/or internal meetings.
• Adhere to all related compliance, safety and monitoring.
• Coordinate communication with all internal and external collaborators.
• Assist with preparations of scientific papers, abstracts and graphs.
• Support Senior Research Coordinator in preparation of proposals, grant budgeting and writing.

Qualifications

Qualifications:

• Bachelor\'s degree in a relevant field of study
• Minimum 3 years previous experience in research studies/clinical trials or other research projects.
• Experience with the management of large clinical research studies and or databases.
• Working knowledge of ICH-GCP Guidelines and international research requirements.
• Highly efficient computer skills, extensive experience with the Microsoft office suite, REDCap and statistical software
• Ability to work independently

Assets:

• Highly developed and problem solving and critical thinking skills.
• Excellent verbal and written communication skills.

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

Hamilton Health Sciences