Clinical Research Coordinator Pediatric HematologyOncology (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
The MUHC Pediatric Hematology/Oncology Research Program aims to promote and improve the health of children and young adults diagnosed with cancer or hematological disorders. We support and conduct research and research training in health and illness with the goal of facilitating the development and implementation of clinical trials biobanks cancer control and nurse-initiated studies and protocols. Ongoing efforts to strengthen the interdisciplinary aspects of research are a priority for us.

This position will participate in the execution of Hematology/Oncology research studies and provide operational support to the Clinical Research Unit (CRU). It is an integral role that will work with Clinical Research Coordinators doctors and the multi-disciplinary team of the division of hematology/oncology and the Montreal Childrens Hospital.


General Duties
Actively participates in the execution of ongoing research projects
Developing and implementing of checklists working instructions and any new SOPs of the CRU
Overseeing and executing quality improvement projects to ensure compliance with research regulations including essential document filing management system
Overseeing and executing fundraising for the CRU including budgeting finances logistics committee meetings and event coordination
Creating and maintaining patient tracking systems and producing reports via multiple software applications liaising with the interdisciplinary team
Filing and organizing research documents (paper and electronic)
Tracking and ongoing management of research required certifications training and regulatory documents such as delegation logs membership rosters safety reports reviews etc.
Archiving of research documents and/or creating certified electronic copies for archiving.
Monitoring and submitting ethical approvals amendments renewals and project contracts in a timely manner
Coordinating a variety of studies related to therapeutics biology tissue banking and quality of life (this includes opening new studies applying for contracts patient recruitment enrolment follow-up and data entry case management of protocol participants data organization and storage and being familiar with research protocols in order to advise the research team)
Interacting with patients and families regarding but not limited to recruitment and questionnaire administration
Extracting and entering data with registries
Adhere to ethical guidelines and Good Clinical Practice (GCP)
Participating in audits and monitoring visits when appropriate
Other tasks as required and assigned by the CRU Manager.

Website of the organization

/ Experience

Education: Diploma of College Studies (DEC)
Other education considered an asset for this position:
Bachelors degree
Certified Clinical Research Professional (through SoCRA or ACRP or equivalent organization) preferred.

Work Experience: Minimum of 2 years of related experience with experience in clinical trials or oncology being an asset.

Required Skills

Excellent communication skills in French and English spoken and written
Proactive
Strong team interpersonal and communication
Adept at using measured persistence in order to obtain required documentation to ensure compliance with research regulations
Extremely detail oriented and organized
Demonstrates active critical thinking and flexibility/adaptability to shifting priorities and multiple projects
Comprehensively use computer software and technology.

Additional information

Status: Temporary full time (35-hour workweek)
Pay Scale: Commensurate with education and experience. $44408.00 - $82427.80
Work Shift: Monday to Friday 8:30am to 4:30pm
Work Site: GLEN Site 1001 boul. Decarie

***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!



learn more about our benefits please visit 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