Clinical Research Coordinator

Found in: Talent CA C2 - 2 weeks ago

Montreal, Canada Research Institute of the McGill University Health Centre Full time

Do you want to work for a world-renowned research institute that pushes the boundaries of biomedical science and health research? Right here in Montreal At the Research Institute of the McGill University Health Centre (RI-MUHC), you can be part of an organization focused on scientific discovery and innovation in patient-centered medicine. Join us today and make a difference

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 with research database platform at the Women’s Health Research Unit.

General Duties

Under the supervision of Dr. Lucy Gilbert, the clinical research coordinator is responsible for coordinating the integration of the gynecologic-oncology clinical data with research database platform 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.

Website of the organization

Education / Experience

• Education: Bachelor's Degree. Preferred to have good medical background, international medical graduates are encouraged to apply,
• Experience in working with electronic patients files,
• Prior experience entering data is an asset,
• Previous oncology experience is an asset.

Required Skills

• Bilingual: English spoken and written, French is an asset,
• Basic computer skills are necessary,
• Independent, flexible, organized and have the ability to work with minimal supervision,
• Ability to work and communicate with a dynamic team,

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