Clinical Research Coordinator (Research Institute)

McGill University Health Centre; Montreal; On-site; CAD 60,000 - 80,000; Full time

Job summary

The Research Institute of the McGill University Health Centre is seeking a clinical research coordinator to oversee the integration of gynecologic-oncology clinical data into research platforms. In this role, you'll ensure data accuracy, facilitate audits, and collaborate with research teams to prepare findings for publication.

Qualifications

• Experience in clinical data collection and management.
• Familiarity with ICH/GCP guidelines.
• Ability to coordinate research activities.

Responsibilities

• Coordinate integration of gynecologic-oncology clinical data.
• Review medical charts and ensure timely data collection.
• Prepare research findings for publication.

Skills

Attention to detail

Data management

Communication

Job description

RESEARCH INSTITUTE OF THE MUHC
The Research Institute of the McGill University Health Centre (RI-MUHC) is a world-renowned biomedical and hospital research centre. Located in Montreal, Quebec, the Institute is the research arm of the McGill University Health Centre (MUHC) affiliated with the Faculty of Medicine at McGill University. The RI-MUHC is supported in part by the Fonds de recherche du Québec - Santé (FRQS).

Position summary
Under the supervision of Dr. Lucy Gilbert, the clinical research coordinator is responsible for coordinating the integration of the gynecologic-oncology clinical data into research database platforms at the Women’s Health Research Unit.

General Duties
• Review medical charts, patient lists, OR lists, and pathology reports for potential participants and understand their disease course,
• Ensure the collection of data as per ICH/GCP in a timely manner,
• Enter the relevant clinical information that include laboratory results, pathology reports, treatment plan, and patient clinical course into the data platform,
• Coordinate with the research team to ensure that the data comply with the quality control standards,
• Identify and correct source data errors.
• Participate in meetings related to research data platform,
• Attend meetings with attending staff when potential participants are discussed and flag eligible patients,
• Gather information for publication purposes.
• Help in preparing research findings and data for publication,
• Prepare sites for audits,
• Answer questions and requests from the sponsors,
• Process and ship biological samples.