Clinical Research Coordinator - Montréal, Canada - Centre universitaire de santé McGill

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Description
Clinical Research Coordinator - Tuberculosis Research and Epidemiology


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 Clinical Research Coordinator will be responsible for the coordination of projects, meeting logistics with other co-investigators, coordination of data collection and support for database management for observational studies and reviews.


General Duties

  • Coordinating projects that evaluate patient costs associated with respiratory diseases and illnesses,
  • Helps with protocol submission to ethics review board, amendments, and annual renewals,
  • Help with literature review and protocol review,
  • Coordinate data collection and interhospital agreements for data sharing,
  • Responsible for review and analysis of research data.
  • Help with data management (mainly with Excel),
  • Obtains the required training for Good Clinical Practice, Tri-Council Course on Research Ethics, etc.,
  • Provide training, as needed, to personnel participating in certain research activities,
  • Provide information to research collaborators,
  • Helps with manuscript preparation,
**To apply: please submit a cover letter, complete CV and two

(2) reference letters in one (1) PDF document**
Website of the organization

Education / Experience

  • DEC in science or related field,
  • Minimum 1 year of clinical research experience,
  • Bilingual: French and English spoken and written,
  • Effective communication, good organization/time management skills and ability to work in a team environment,
  • Must be selfdirected and possess a strong initiative to work independently,
  • Autonomous, flexible sense of ethics and good judgment,
  • Excellent interpersonal skills,
  • Excellent organization, ability to multitask and prioritize timesensitive issues ,
  • Proficiency in MS Office (Word, Excel),
  • Previous knowledge of database management and statistics are assets,
  • Previous experience with database softwares (RStudio, SPSS, Access, etc )
  • Knowledge of international, federal and provincial laws and regulations governing clinical research (ICH
  • GCP) is an asset.

Additional information

Status:
Part-time, yearly renewal


Pay Scale:
Commensurate with education and experience / : $43, $80,425.80


Work Shift:
Variable, up to 7 hours per week


Work Site:
Glen site

Why work with us?

  • 4week 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

THIS IS NOT A HOSPITAL POSITION.
**Equal Opportunity Employment Program

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