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

Centre universitaire de santé McGill

Verified Company

Montréal, Canada

2 weeks ago

Posted by:

Sophia Lee

beBee Recruiter

Description

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

General Duties

Coordinating multicentre projects that evaluate resource use/workforce organization in Tuberculosis Treatment and how they correlate with costs
Helps with protocol submission to ethics review board, amendments, and annual renewals
Help with literature review and protocol review,
Oversees care to assure protocol adherence is maintained by staff, serve internally as a resource for nursing, medical staff and research staff,
Coordinate multicentre data collection and interhospital agreements for data sharing
Responsible for collection and documentation of research data for designated patients.
Help with data management (mainly with Excel),
Monitors care of patients in accordance with research protocols and Good Clinical Practices and takes action to assure that patient care is delivered in accordance with policies of the particular care setting.
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
Assist with student supervision for research projects and data analysis
Provide information to research collaborators
Helps with manuscripts and Health Canada documents 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:
Temporary, part-time, yearly renewal

Pay Scale:
$ $43.11 Commensurate with education and experience

Work Shift:
Varialb,e up to 5 hours per week

Work Site:
Glen Site

THIS IS NOT A HOSPITAL POSITION.
Equal Opportunity Employment Program