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Research Coordinator

2 months ago

Edmonton, Alberta, Canada Alberta Health Services Full time

About the Opportunity:

Alberta Health Services is a leading academic health sciences centre with a reputation for clinical research, innovation, education, and patient-centred care. Our Clinical Trial Unit (CTU) is a specialty area where clinical researchers design, conduct, analyze, and publish clinical trials and other health studies. The CTU is currently recruiting for a Lead Clinical Research Coordinator (LCRC); you will be assigned to the Gastrointestinal and Liver Disease Research Group (GILDR). The GILDR Group is an energetic and experienced team of physicians and research nurses. Our team has gained recognition internationally for their excellence in managing and conducting all aspects of clinical trials. The GILDR team focuses on conducting clinical trials and research studies with outcomes that aim to improve the quality of life for those patients who suffer from gastrointestinal or liver disease.

Key Responsibilities:

  • Bring exceptional management skills, including planning, implementation, resource allocation, and oversight of multiple clinical trials from feasibility to close out.
  • Ensure clinical trial activities are on time, within budget, and scope.
  • Provide day-to-day oversight of GILDR, including financial administration, budgets, and contracts.
  • Maintain established operating procedures and working practices that govern the research team's activities.
  • Organize and lead staff meetings, participate in hiring, evaluate staff, participate in site selection visits, site initiation visits, and meet with monitors when on site to resolve any issues or problems.
  • Assist with regulatory applications, drafting informed consents, source documents, and working templates as required.

About the Role:

As a Research II, you will be responsible for coordinating research activities that generate and disseminate new knowledge that assists with advancing the understanding of health disciplines and various health and medical concerns. Working with the principal investigator, you will assist with the study design and development of research protocols, determine appropriate data collection methods and measurement procedures, interpret results, develop recommendations, and coordinate study approvals. You will also contribute to grant submissions and budgeting, conduct literature reviews and environmental scans, and provide day-to-day oversight of research studies/projects.

Required Qualifications:

  • Master's degree in a health or science-related field.
  • Registration with applicable professional association or college where required.

Preferred Qualifications:

  • Experience with electronic data capture and database programs (RAVE).
  • Knowledge of AHS patient care information systems like Connect Care.
  • Experience with developing and reviewing standard operating procedures and working policies.