Clinical Research Coordinator - CVIS & IDIGH (Research Institute)
Top Benefits
About the role
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 We are currently seeking a highly motivated, organized, enthusiastic individual to join our dynamic team. Under the direct supervision of the principal investigator, the incumbent will participate in the recruitment and follow-up of participants for patient-centered studies focused on HIV care:
- Evaluate a model for rapid initiation of antiretroviral therapy at the Chronic Viral Illness Service of the McGill University Health Center,
- Implementation of a mobile application to monitor people living with HIV in the Chronic Viral Illness Service.
- Preparation and implementation of projects aimed at assessing needs and deploying technological tools to reduce barriers to preventive and therapeutic HIV care for individuals from key communities (e.g., migrant populations, gbMSM men, etc.).
The incumbent will be part of a multidisciplinary clinical research team with a variety of expertise and will thus be able to train in a wide variety of tasks.
General Duties Responsibilities May Include But Are Not Necessarily Limited To
- Coordinate patient recruitment and study procedures for 3 studies:
- Identifying eligible participants,
- Scheduling study visits,
- Explaining and reviewing informed consent form with participants,
- Performing chart review,
- Completing case report forms and questionnaires with participants,
- Organizing biological specimen collection,
- Timely completion of all study documentation forms, including case report forms (CRFs), queries and other study specific documents,
- Coordinating and collaborating with the many team members of the Chronic Viral Illness Service at the MUHC, laboratory team at Jewish General Hospital, SIDEP+ and the two satellite sites,
- Attending relevant departmental meetings or rounds in order to increase knowledge and understanding.
- Assist the investigator with administrative tasks:
- Assisting in the development of ICFs, questionnaires, and editing protocols for studies and ethics submission.
- Performing miscellaneous job-related duties as assigned by supervisor, including support to other coordinators, students, and research staff members.
- Communications and knowledge translation and dissemination:
- Managing study site supervision including correspondence, training, queries and general site support,
- Engaging with the different stakeholders of the ASAP project which can include nurses, pharmacists, physicians, lawyers, and laboratory scientists,
- Valuing multidisciplinary clinical research methods of study with a team of healthcare professionals dedicated to serving vulnerable HIV populations,
- Supporting the challenges faced by vulnerable populations such as culture diversities, sexualities, generational gaps, and socioeconomics,
- Assisting in the preparation and submission of abstracts and manuscripts,
- You may be asked to assist with design/development of promotional materials/newsletters,
- Grant and publication reviewing/writing.
Website of the organization
Education / Experience
Education: Diploma of College Studies (DEC)
Field of Study: Science, preferably in a field related to health
Other education considered an asset for this position: Candidates with a Bachelor’s degree and significant relevant experience or with a Master’s degree will also be considered.
Work Experience: 1 year of experience recruiting and following participants participating in research protocols.
Required Skills
- Excellent command of English and French, both spoken and written,
- High level of initiative and organization,
- Ability to prioritize and to multitask,
- Ability to acquire new skills of overlapping disciplines in health and social sciences, while adapting to new situations,
- Sensitivity to the challenges of cultural, sexual, generational and gender diversity,
- Demonstrated ability to work independently as well as within a team,
- Ability to exercise tact and discretion with vulnerable populations and maintain confidentiality,
- Computer skills, including Microsoft Word, Excel, PowerPoint and Access,
- Experience with REBs, HIV and/or Hepatitis C would also be an asset.
Additional information
Status: Temporary, full time (35-hour workweek)
Pay Scale: $44,408.00- $82,427.80. Commensurate with education and experience
Work Shift: Monday to Friday 8:30am to 4:30pm.
Work Site: 5252 boul. de Maisonneuve
If other, please specify: and MUHC Glen site.
*** If you wish to include a cover letter, please attach it with your resume in one document. ***
Why work with us?
- 4-week vacation, 5th week after 5 years,
- Bank of 12 paid days (personal days and days for sickness or family obligations),
- 13 paid statutory holidays,
- Modular group insurance plan (including gender affirmation coverage),
- Telemedicine,
- RREGOP (defined benefit government pension plan),
- Training and professional development opportunities,
- Child Care Centres,
- Corporate Discounts (OPUS + Perkopolis),
- Competitive monthly parking rate,
- Employee Assistance Program,
- Recognition Program,
- Flex work options and much more!
To learn more about our benefits, please visit http://rimuhc.ca/en/compensation-and-benefits
THIS IS NOT A HOSPITAL POSITION. Equal Opportunity Employment Program
The Research Institute of the McGill University Health Centre hires on the basis of merit and is strongly committed to equity, diversity and inclusion within its community. We welcome applications from all qualified candidates who self-identify as members of racialized groups/visible minorities, women, Indigenous persons, persons with disabilities, ethnic minorities, and 2SLGBTQIA+ persons. We also welcome candidates with the skills and knowledge to productively engage with diverse communities. Persons with disabilities who anticipate needing accommodations for any part of the application process may confidentially contact, research.talent@muhc.mcgill.ca
About RI-MUHC | Research Institute of the MUHC | #rimuhc
The Research Institute of the McGill University Health Centre (The Institute) brings together pediatric and adult research programs, accelerating the translation of biomedical research to improve human health.
Clinical Research Coordinator - CVIS & IDIGH (Research Institute)
Top Benefits
About the role
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 We are currently seeking a highly motivated, organized, enthusiastic individual to join our dynamic team. Under the direct supervision of the principal investigator, the incumbent will participate in the recruitment and follow-up of participants for patient-centered studies focused on HIV care:
- Evaluate a model for rapid initiation of antiretroviral therapy at the Chronic Viral Illness Service of the McGill University Health Center,
- Implementation of a mobile application to monitor people living with HIV in the Chronic Viral Illness Service.
- Preparation and implementation of projects aimed at assessing needs and deploying technological tools to reduce barriers to preventive and therapeutic HIV care for individuals from key communities (e.g., migrant populations, gbMSM men, etc.).
The incumbent will be part of a multidisciplinary clinical research team with a variety of expertise and will thus be able to train in a wide variety of tasks.
General Duties Responsibilities May Include But Are Not Necessarily Limited To
- Coordinate patient recruitment and study procedures for 3 studies:
- Identifying eligible participants,
- Scheduling study visits,
- Explaining and reviewing informed consent form with participants,
- Performing chart review,
- Completing case report forms and questionnaires with participants,
- Organizing biological specimen collection,
- Timely completion of all study documentation forms, including case report forms (CRFs), queries and other study specific documents,
- Coordinating and collaborating with the many team members of the Chronic Viral Illness Service at the MUHC, laboratory team at Jewish General Hospital, SIDEP+ and the two satellite sites,
- Attending relevant departmental meetings or rounds in order to increase knowledge and understanding.
- Assist the investigator with administrative tasks:
- Assisting in the development of ICFs, questionnaires, and editing protocols for studies and ethics submission.
- Performing miscellaneous job-related duties as assigned by supervisor, including support to other coordinators, students, and research staff members.
- Communications and knowledge translation and dissemination:
- Managing study site supervision including correspondence, training, queries and general site support,
- Engaging with the different stakeholders of the ASAP project which can include nurses, pharmacists, physicians, lawyers, and laboratory scientists,
- Valuing multidisciplinary clinical research methods of study with a team of healthcare professionals dedicated to serving vulnerable HIV populations,
- Supporting the challenges faced by vulnerable populations such as culture diversities, sexualities, generational gaps, and socioeconomics,
- Assisting in the preparation and submission of abstracts and manuscripts,
- You may be asked to assist with design/development of promotional materials/newsletters,
- Grant and publication reviewing/writing.
Website of the organization
Education / Experience
Education: Diploma of College Studies (DEC)
Field of Study: Science, preferably in a field related to health
Other education considered an asset for this position: Candidates with a Bachelor’s degree and significant relevant experience or with a Master’s degree will also be considered.
Work Experience: 1 year of experience recruiting and following participants participating in research protocols.
Required Skills
- Excellent command of English and French, both spoken and written,
- High level of initiative and organization,
- Ability to prioritize and to multitask,
- Ability to acquire new skills of overlapping disciplines in health and social sciences, while adapting to new situations,
- Sensitivity to the challenges of cultural, sexual, generational and gender diversity,
- Demonstrated ability to work independently as well as within a team,
- Ability to exercise tact and discretion with vulnerable populations and maintain confidentiality,
- Computer skills, including Microsoft Word, Excel, PowerPoint and Access,
- Experience with REBs, HIV and/or Hepatitis C would also be an asset.
Additional information
Status: Temporary, full time (35-hour workweek)
Pay Scale: $44,408.00- $82,427.80. Commensurate with education and experience
Work Shift: Monday to Friday 8:30am to 4:30pm.
Work Site: 5252 boul. de Maisonneuve
If other, please specify: and MUHC Glen site.
*** If you wish to include a cover letter, please attach it with your resume in one document. ***
Why work with us?
- 4-week vacation, 5th week after 5 years,
- Bank of 12 paid days (personal days and days for sickness or family obligations),
- 13 paid statutory holidays,
- Modular group insurance plan (including gender affirmation coverage),
- Telemedicine,
- RREGOP (defined benefit government pension plan),
- Training and professional development opportunities,
- Child Care Centres,
- Corporate Discounts (OPUS + Perkopolis),
- Competitive monthly parking rate,
- Employee Assistance Program,
- Recognition Program,
- Flex work options and much more!
To learn more about our benefits, please visit http://rimuhc.ca/en/compensation-and-benefits
THIS IS NOT A HOSPITAL POSITION. Equal Opportunity Employment Program
The Research Institute of the McGill University Health Centre hires on the basis of merit and is strongly committed to equity, diversity and inclusion within its community. We welcome applications from all qualified candidates who self-identify as members of racialized groups/visible minorities, women, Indigenous persons, persons with disabilities, ethnic minorities, and 2SLGBTQIA+ persons. We also welcome candidates with the skills and knowledge to productively engage with diverse communities. Persons with disabilities who anticipate needing accommodations for any part of the application process may confidentially contact, research.talent@muhc.mcgill.ca
About RI-MUHC | Research Institute of the MUHC | #rimuhc
The Research Institute of the McGill University Health Centre (The Institute) brings together pediatric and adult research programs, accelerating the translation of biomedical research to improve human health.