Research Coordinator
@ Hamilton Health Sciences

Hamilton, Ontario, Canada
On Site
Part-time
Posted 3 days ago

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Job Details

Overview

The Research Coordinator’s purpose is to lead a team in the conduct of one or more research studies. This role involves working closely with the Principal Investigator (PI) and/or Program Manager (PM) and managing key aspects of research projects.

Key Responsibilities

  • Act as the primary contact for internal support departments and external stakeholders.
  • Develop and monitor study timelines.
  • Coordinate and direct data management methodologies and site management practices.
  • Prepare ethics, regulatory, and health authority documentation per ICH-GCP guidelines.
  • Coordinate training, site monitoring, and regular meetings with study stakeholders.
  • Assist in research study budgets, grant proposals, and finance management.

Requirements

  • Bachelor's degree in a relevant field.
  • Minimum 3 years of experience with multi-center research studies or clinical trials.
  • Experience with managing large clinical research studies and databases.
  • Working knowledge of ICH-GCP Guidelines and international research requirements.
  • Proficient in Microsoft Office and strong computer skills.
  • Supervisory experience and team coordination skills.

Key skills/competency

  • Project Management
  • Data Management
  • Stakeholder Communication
  • Regulatory Documentation
  • Team Coordination
  • Budget Management
  • ICH-GCP
  • Clinical Trials
  • Presentation Skills
  • Microsoft Office

How to Get Hired at Hamilton Health Sciences

🎯 Tips for Getting Hired

  • Research Hamilton Health Sciences culture: Understand their mission, values, and news.
  • Customize your resume: Highlight research coordination and project management skills.
  • Emphasize technical expertise: Include ICH-GCP and clinical trial experience.
  • Prepare for interviews: Be ready to discuss team leadership and study management.
  • Follow up: Connect with the hiring manager via email.

📝 Interview Preparation Advice

Technical Preparation

Review ICH-GCP guidelines.
Practice data management tools.
Study clinical trial documentation.
Familiarize with Microsoft Office.

Behavioral Questions

Describe team conflict resolution.
Explain time management strategies.
Discuss coordination with external stakeholders.
Share supervisory experience examples.

Frequently Asked Questions