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Clinical Research Associate

2 months ago


Hamilton, Ontario, Canada Hamilton Health Sciences Full time
Job Summary

The Clinical Research Associate will be responsible for the organization, administration, and coordination of assigned clinical research tasks, ensuring the quality and integrity of clinical trial data.

Key Responsibilities
  • Coordinate and manage clinical research studies, including startup procedures, patient screening, and data collection.
  • Monitor study compliance and maintain accurate records.
  • Collaborate with multidisciplinary teams to facilitate patient recruitment and participation in clinical research.
  • Develop and implement effective data flow systems.
  • Provide excellent communication and interpersonal skills to interact with patients, investigators, and other stakeholders.
Requirements
  • Graduate of a Community College Secretarial/Office Administrative Diploma Program or equivalent.
  • Minimum three years of recent experience in an oncology-related environment.
  • Minimum two years of recent clinical research experience or equivalent education.
  • Certification as a Clinical Research Professional or Clinical Research Coordinator is preferred.
  • Strong analytical skills with attention to detail.
  • Excellent organizational skills and ability to prioritize workload.
  • Ability to travel between HHS sites to support off-site investigators.
About Hamilton Health Sciences

Hamilton Health Sciences fosters a culture of patient and staff safety, guided by our Mission, Vision, Values, and Values-Based Code of Conduct. We are a teaching hospital and expect all staff and physicians to support students and other learners.

We are an equal opportunity employer and will accommodate any needs under the Canadian Charter of Rights and Freedom, Accessibility for Ontarians with Disabilities Act, and the Ontario Human Rights Code.