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 Quebec - Sante (FRQS).
Position summary
Under the supervision of the Manager of the Centre for Innovative Medicine (CIM) Oncology Research Program as well as following established governmental guidelines and regulations, the incumbent is responsible for the supervision of the clinical research staff (Oncology).
General Duties

• Supervises clinical research staff,
• Participates in the start-up of new studies (from the Confidential Disclosure agreement until the conduct of the initiation visit),
• Assigns staff to studies and maintain a balanced staff/study ratio,
• Ensures that the research team meets the study recruitment objectives and implements solutions to meet the required objectives,
• Responsible for monitoring patient research charts ensuring compliance with working instructions, SOPs, ALCOA and more.
• Holds regular meetings with the staff to ensure that they meet quality standards and regulations,
• Provides the manager with bi-weekly reports on the status of the studies,
• Works closely with investigators including regular communications and troubleshoot when needed,
• Responsible for the training of new staff and ensuring that all internal and external training are up-to-date GCP, SOP, Health Canada Div 5, IATA, Code Blue/Crash cart, CPR, etc...,
• Responsible to put in place a back-up plan for all research projects to ensure studies are not interrupted,
• Responsible for staffsaEUR(TM) performance and conduct annual performance reviews,
• Participates in the interviews of new staff,
• Meets employees weekly or biweekly,
• Meets with his/her manager biweekly,
• Daily troubleshooting,
• Any other tasks requested by the Manager.

Website of the organization
https://rimuhc.ca/en
Education / Experience
o UndergraduateaEUR(TM)s Degree in a health-related field
o Minimum of 7 years of experience conducting clinical research studies in a hospital environment,
o Experience in the pharmaceutical industry,
o Clinical research accreditation (SoCRA) is required,
o Bilingual (French and English, verbal and written),
o Ability to work under pressure,
o Excellent organizational skills, ability to multi-task and prioritizing time-sensitive issues,
o Experience working with electronic data management systems, tools and technologies (EDC),
o Experience working with Clinical Trial Management System (CTMS),
o Excellent knowledge of international, federal and provincial laws and regulations governing clinical research (ICH-GCP),
o Self-directed and organized.
o Able to work as part of a team,
o Excellent interpersonal skills.
Additional information
Status : Full-time
Pay Scale : commensurate with qualifications and experience
Work Shift : 8:30 a.m. to 4:30 p.m. (Mondays-Fridays). Must be available to work outside office hours.
Work Site : Glen site (1001 Decarie)
This position requires adequate protection against COVID-19 in light of work site and as per the Government of Quebec decree # 1276-2021 dated September 24, 2021
https://rimuhc.ca/careers
To learn more about our benefits, please visit http://rimuhc.ca/en/compensation-and-benefits
THIS IS NOT A HOSPITAL POSITION.
NOTE: The masculine gender has been used for brevity and includes the feminine gender.
Equal Opportunity Employment Program
Le CUSM applique un programme daEUR(TM)accas a laEUR(TM)egalite en emploi et invite les femmes, les Autochtones, les minorites visibles, les minorites ethniques et les personnes handicapees a presenter leur candidature. Des mesures daEUR(TM)adaptation peuvent atre offertes aux personnes handicapees qui en font la demande en fonction de leurs besoins.