Clinical Research Coordinator - Nurse

Job summary

Coordinate multiple clinical research studies and support overall patient management in collaboration with investigators and healthcare personnel. Obtain consent, assess eligibility, monitor safety and medication compliance, maintain study documentation, coordinate data collection, respond to study queries, and prepare ethics submissions.

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 Under the supervision of the Manager, Pediatric and Adult Research, Centre for Innovative Medicine (CIM), the Clinical Research Coordinator - Nurse is responsible for supporting the successful conduct of clinical research studies. The incumbent will collaborate with Investigators and health care personnel to assume responsibility for the overall patient management and the coordination of several clinical studies for the Pediatric and Adult Department of the RI-MUHC. The Centre for Innovative Medicine is a hospital which is a unique center in Canada of 5000 m2 dedicated exclusively to clinical research. The CMI is located at the MUHC Glen site. General Duties Obtains informed consent, assesses patients for protocol eligibility through personal interviews and/or medical record review in in-patient and out-patient settings, Maintains and completes concomitant medication, adverse events and questionnaires logs, forms and protocol specific source documentation, Monitors patient safety and medication compliance, Prepares orders for protocol-related requests and procedures, consults, requests for pathology slides and blocks as needed, Coordinates all aspects of data collection and source documentation, Completes all research-related documents and responds to queries and requests for information, Conducts protocol specific and scientific trainings, Responsible for the Research Ethics Board submissions, Conduct other related tasks as assigned by the supervisor. Website of the organization https://rimuhc.ca/en Education / Experience DEC in Nursing is required, Good-standing member of the OIIQ, Minimum four (4) years of nursing experience including two (2) years in a hospital setting, Experience with pediatric patients, Required Skills Bilingual: French and English spoken and written, Solid written and verbal communication skills, Able to work under minimal supervision, Self-directed, flexible, organized and sense of ethics, Clinical research experience is an asset, Knowledge of international, federal and provincial laws and regulations governing clinical research (ICH-GCP) is an asset. Additional information Status : Temporary full time (35 hours/weeks - 12-month contract) Pay Scale: $45,518.20 to $84,484.40/year Commensurate with education and experience Work Shift: Monday to Friday from 8:30 am to 4:30 pm (Flexible) Work Site: Glen site, 1001, de Maisonneuve ***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 multiple clinical research studies and support overall patient management in collaboration with investigators and healthcare personnel. Obtain consent, assess eligibility, monitor safety and medication compliance, maintain study documentation, coordinate data collection, respond to study queries, and prepare ethics submissions.

Requirements

A nursing DEC and good-standing membership with the OIIQ are required, along with at least four years of nursing experience, including two years in a hospital setting, and experience with pediatric patients. French and English fluency in speaking and writing is required; clinical research experience and knowledge of ICH-GCP and applicable research regulations are assets.

Benefits

• Four Weeks of Vacation
• Additional Vacation After Five Years
• 12 Paid Personal, Sick, and Family Obligation Days
• 13 Paid Statutory Holidays
• Modular Group Insurance
• Gender Affirmation Coverage
• Telemedicine
• Defined Benefit Pension Plan
• Training and Professional Development
• Child Care Centres
• Corporate Discounts
• Competitive Monthly Parking
• Employee Assistance Program
• Recognition Program
• Flexible Work Options

Listed skills

• written communication · Preferred
• Organization · Preferred
• self-direction · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

• Informed Consent
• Patient Eligibility Assessment
• Patient Safety Monitoring
• Medication Compliance Monitoring
• Clinical Data Collection
• Source Documentation
• Adverse Event Documentation
• Research Ethics Board Submissions
• Clinical Research Coordination
• Protocol Training
• Written Communication
• Verbal Communication
• Organization
• Self-Direction
• Flexibility
• Ethical Judgment

Job areas

• Healthcare
• Science & Research

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