Research Coordinator
Hamilton, ON · On-site
Provide coordination and direction in the development of data management methodologies for multiple ... and REDCap * Supervisory experience and team coordination. * Experience performing systematic ...
Hamilton, ON · On-site
Provide coordination and direction in the development of data management methodologies for multiple ... and REDCap * Supervisory experience and team coordination. * Experience performing systematic ...
Hamilton, ON · On-site
Provide coordination and direction in the development of data management methodologies for multiple ... and REDCap * Supervisory experience and team coordination. * Experience performing systematic ...
Design, develop, and maintain surveys and data collection instruments in REDCap, including using ... Prepare and manage Research Ethics Board (REB) applications, amendments, and continuing review ...
Quick apply
Design, develop, and maintain surveys and data collection instruments in REDCap, including using ... Prepare and manage Research Ethics Board (REB) applications, amendments, and continuing review ...
CA$39K - CA$54K/yr
Strong organizational and time-management skills; able to manage multiple participants, visits, and ... data entry systems (e.g., REDCap, LORIS) is an asset. * Prior experience with Alzheimer's or ...
New
CA$39K - CA$54K/yr
Strong organizational and time-management skills; able to manage multiple participants, visits, and ... data entry systems (e.g., REDCap, LORIS) is an asset. * Prior experience with Alzheimer's or ...
New
CA$58K - CA$72K/yr
Experience with data capture applications (e.g. REDCap) * Ability to function independently and as part of a team * Excellent interpersonal, time management, and organizational skills Compensation At ...
CA$58K - CA$72K/yr
Experience with data capture applications (e.g. REDCap) * Ability to function independently and as part of a team * Excellent interpersonal, time management, and organizational skills Compensation At ...
Full-time
Re-posted 24 days ago
The Research Coordinator's purpose is to lead a team in the conduct of one or more research studies. The Research Coordinator is accountable to the Principal Investigator (PI) and or Program Manager (PM) and is responsible for all aspects of research projects highlighted below.
Act as the primary contact for internal support departments and external stakeholders.
Development and monitoring of study timelines.
Provide coordination and direction in the development of data management methodologies for multiple studies; including key data management methods.
Provide coordination and direction in the development of site management practices for multiple studies; including collection 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 key study specific stakeholders.
Prepare presentations for external and/or internal meetings.
Adhere to all related compliance, safety and monitoring.
Prepare all ethics and regulatory documents in accordance with the institution and regulatory and GCP guidelines.
Coordinate communication with all internal and external collaborators.
Coordinate training of study teams/centers on all aspects of clinical study procedures.
Coordinate /perform site monitoring and site visits to confirm adherence to study protocol, procedures, ICH-GCP guidelines, local and national regulations and guidelines.
Help develop research study budgets, in collaboration with PI's and other collaborators.
Help administer multiple study and sub-study accounts.
Negotiate budgets with vendors, sites and other collaborators.
Support Principal Investigator(s) in preparation of proposals, grant budgeting and writing, and writing of study manuscripts
Manage day to day study finance and study budgeting.
Screen, recruit, consent, and follow participants from studies
Develop study-related materials (print, web-based, etc.)
Oversee data collection and management, including the development and implementation of data quality rules, followed by query-sending and resolution
Bachelor's degree in a relevant field of study.
Minimum 3 years previous experience in multi-center research studies/clinical trials or other research projects.
Documented experience working on randomized trials for at least 2 years
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, Covidence, and REDCap
Supervisory experience and team coordination.
Experience performing systematic reviews