Clinical Research Coordinator – Oncology (Research Institute)

Job title:

Clinical Research Coordinator – Oncology (Research Institute)

Company

McGill University Health Centre

Job description

Job Number:J0524-1499Job Title:Clinical Research Coordinator – Oncology (Research Institute)Organisation:Research Institute of the MUHCWork Location:SITE GLENJob Category:Administration, human ressources and financeJob Type:Full timeSalary:$43,316.00 – $80,425.80 /YearShift:DayOpen Positions:1Le Centre universitaire de santé McGill (CUSM) est un centre hospitalier universitaire intégré, reconnu à l’échelle internationale pour l’excellence de ses programmes cliniques, de sa recherche et de son enseignement. Le CUSM a pour objectif d’assurer aux patients des soins fondés sur les connaissances les plus avancées dans le domaine de la santé et de contribuer au progrès des connaissances.Job DescriptionRESEARCH 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 of Oncology Research, Centre for Innovative Medicine (CIM), the Oncology Clinical Research Coordinator is responsible for supporting the successful conduct of clinical research studies in oncology. The Clinical Research Coordinator collaborates with Investigators and health care personnel to assume responsibility for the overall patient management and coordination of several clinical studies for the CIM-Oncology Department of the RI-MUHC.The Centre for Innovative Medicine is located in the new Glen site hospital which is a unique center in Canada of 5000 m2 dedicated exclusively to clinical research.http://rimuhc.ca/web/research-institute-muhc/centre-for-innovative-medicineGeneral Duties

• Recruits research participants, prescreens patients and obtains informed consent,
• Assesses patients for protocol eligibility through personal interviews and/or medical record review in in-patient and out-patient settings,
• Maintains, completes and updates, concomitant and adverse event logs and questionnaires and protocol specific source documentation,
• Completes patient charting accordingly,
• Coordinates protocol related tests, i.e, venipuncture including sample collection, Pharmacokinetics (PKs), Pharmacodynamics (PDs), urine collection and Electrocardiogram (ECG),
• Processes and shipments of samples according to clinical protocol and manuals,
• Create study specific source documentation, i.e, study visits, AE and Conmed logs, study imaging forms, pathology request forms, ICF tracking log prior to study activation, and other study related forms,
• Provides coordination of all aspects of data collection and source documentation,
• Maintains and updates regularly the study lab kit inventory logs, destroys expired kits and requests study kits as needed,
• Schedules site initiation visits, monitoring visits and follows-up with issues identified,
• Acts as a liaison with the radiation and medical oncology groups,
• Conduct other related tasks as assigned by supervisor.

Website of the organizationEducation / ExperienceEducation:

• DEC in sciences or a related field.

Experience:

• Minimum 1 year of clinical research experience,
• Experience in a hospital/clinical setting is an asset,
• Experience in hematology and/or oncology is an asset.

Required Skills

• Bilingual: French and English spoken and written,
• Critical thinking an asset,
• Solid written and verbal communication skills,
• Autonomous, flexible sense of ethics and good judgment,
• Excellent interpersonal skills,
• Excellent organization, ability to multitasks and prioritize time-sensitive issues,
• Ability to work under minimal supervision,
• Proficiency in MS Office (Word, Excel),
• Clinical research experience is an asset,
• Knowledge of international, federal and provincial laws and regulations governing clinical research (ICH-GCP) is an asset.

Additional informationStatus : Full time
Pay Scale: 43,316.00$ à 80,425.80$ commensurate with qualifications and experience
Work Shift: from 8:30 a.m. to 4:30 p.m., Mondays to Fridays
Work Site: Glen siteWhy 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/careersTo learn more about our benefits, please visitTHIS IS NOT A HOSPITAL POSITION.Equal Opportunity Employment ProgramThe 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,

Expected salary

$43316 per year

Location

Montreal, QC

Job date

Wed, 29 May 2024 06:03:50 GMT

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