Clinical Research Coordinator

Job summary

Coordinate a five-year study to improve access to hepatitis C treatment for people in three Montreal provincial prisons, serving as a liaison among the principal investigator, research team, recruitment sites, and community partners. Support study document development, ethics submissions, logistics, recruitment, data collection, research records, and preparation of abstracts and manuscripts.

Job details

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 Department / Research Program: CVIS / IDIGH We are seeking a highly motivated, organized and enthusiastic individual to join our dynamic team. Under the immediate supervision of the principal investigator, the incumbent will be responsible for supporting the successful conduct and coordination of a 5-year study focused on improving access to hepatitis C treatment for people in 3 provincial prisons in Montreal, Quebec. The incumbent will act as the direct link between the principal investigator, the research team, and the external stakeholders, including study recruitment sites and community partners. General Duties Assisting in the development of study protocols, consent forms, questionnaires, and other study documents, Assisting with ethic submissions and amendments, Assisting with logistics and communication between study partners Assisting with participant recruitment, data collection, and storing of study documents according to the research protocol, Ensuring proper and efficient documentation and research organization in a timely manner, Assisting in the preparation and submission of abstracts and manuscripts, Performing other job-related tasks as assigned by the supervisor, including support to other investigators and research coordinators. Standards of performance Respects policies and procedures , Takes initiative and is resourceful, Ability to multitask, Demonstrates attention to detail. Website of the organization https://rimuhc.ca/en Education / Experience Education: Bachelor's Degree Field of Study: Public Health, Epidemiology, or other related field Other education considered an asset for this position: Master’s Degree Work Experience: Minimum of two years of clinical research experience in an academic environment and/or a clinical research organization is required. Experience working with underserved populations is a strong asset. Experience in the field of sexually transmitted and blood-borne infections (STBBIs) is also considered an asset. Required Skills This position requires an advanced knowledge of oral and written French., An advanced knowledge of oral and written English is required, as the position requires regular and complex contact with patients who are exclusively proficient in English. The position also requires complex writing or in-depth analysis of documents in English related to a research project. Excellent communication and interpersonal skills, Ability to work independently or with teams with minimum supervision, Strong sense of organization and high degree of efficiency, Knowledge of Microsoft Office (Word, Excel, Power Point and Outlook), Programming skills in R or a similar program is an asset. Additional information Status: Temporary, full time (35-hour workweek) Pay Scale: Commensurate with education and experience Work Shift: Monday to Friday 8:00am to 4:00pm Work Site: 5252 de Maisonneuve Blvd. ☒ This position offers the possibility of a hybrid work arrangement (on-site and remote). ☒ This position requires to work on several sites. Additional specifications: Must have access to a vehicle for travel required as part of the position. ***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! 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. 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

What you’ll do

Coordinate a five-year study to improve access to hepatitis C treatment for people in three Montreal provincial prisons, serving as a liaison among the principal investigator, research team, recruitment sites, and community partners. Support study document development, ethics submissions, logistics, recruitment, data collection, research records, and preparation of abstracts and manuscripts.

Requirements

A bachelor's degree in public health, epidemiology, or a related field and at least two years of clinical research experience in an academic environment or clinical research organization are required. Advanced spoken and written French and English, strong communication and organizational skills, and proficiency with Microsoft Office are required; experience with underserved populations or sexually transmitted and blood-borne infections is an asset.

Benefits

• Four Weeks of Vacation
• Paid Personal, Sick, and Family Obligation Days
• Paid Statutory Holidays
• Modular Group Insurance
• Telemedicine
• Defined Benefit Pension Plan
• Training and Professional Development
• Child Care Centres
• Corporate Discounts
• Employee Assistance Program
• Recognition Program
• Flexible Work Options

Listed skills

• Communication · Preferred
• interpersonal skills · Preferred
• Organization · Preferred
• Attention to detail · Preferred
• Multitasking · Preferred
• Microsoft Word · Preferred
• Microsoft Excel · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

• Clinical Research Coordination
• Study Protocol Development
• Ethics Submissions
• Participant Recruitment
• Data Collection
• Research Documentation
• Research Organization
• Scientific Writing
• Communication
• Interpersonal Skills
• Organization
• Attention to Detail
• Multitasking
• Microsoft Word
• Microsoft Excel
• R Programming

Job areas

• Science & Research
• Healthcare
• Data & Analytics

More jobs from RI-MUHC | Research Institute of the MUHC | #rimuhc