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Clinical Research Coordinator

1 month ago

Toronto, Ontario, Canada LMC Healthcare Full time
Job Title: Clinical Research Coordinator

About the Role:
LMC Healthcare is seeking a highly skilled Clinical Research Coordinator to join our Data Science Team on a temporary full-time basis. As a Clinical Research Coordinator, you will play a crucial role in supporting our research studies by managing day-to-day tracking of patient progress and data. Your responsibilities will include gaining familiarity with protocols and case report forms, supporting accurate and timely data entry, and assisting with medical chart screening and database query reviews. You will also be responsible for preparing research and participant binders, performing receipt, storage, and organization of study materials, and generating automated and ad hoc reports to support data integrity and database maintenance of the LMC Diabetes Registry.

Responsibilities:
  • Manage day-to-day tracking of patient progress and data in ongoing research studies
  • Gain familiarity of protocols and case report forms (CRFs)
  • Support with accurate, complete, and timely data entry into large databases, and electronic or paper CRFs
  • Assist with medical chart screening and database query reviews to support participant recruitment
  • Assist with informed consent activities, and data management queries and follow-up
  • Medical chart review and data extraction
  • Support with the creation and quality control of research source documents
  • Prepare research and participant binders, as required
  • Perform receipt, storage, and organization of study materials, as required
  • Perform other administrative and clerical duties, as required by the Data Science team and Investigators
  • Generate automated and ad hoc reports to support data integrity and database maintenance of the LMC Diabetes Registry
  • Attend regularly scheduled Data Science team meetings and research training and meetings, as required
  • Conduct literature reviews and synthesize the findings in a clear and efficient manner
  • Assist with preparation of written materials: research ethics board applications, ClinicalTrials.gov registration, study protocols, consent forms, education program surveys, research and program reports, and manuscript, abstract and poster submissions
  • Effectively communicate and present results to the Data Science team, Investigators and staff

Requirements:
  • Bachelors of Science degree or equivalent
  • Masters degree preferred
  • 2+ years experience with clinical research
  • Proficiency with MS Word, Excel, PowerPoint and Outlook