Clinical Research Coordinator

2 weeks ago

Montréal, Canada Centre universitaire de santé McGill Full time

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
Laboratories of Dr. Joanna Przybyl and Dr. Shuk On Annie Leung, are seeking a Clinical Research Coordinator to participate in translational cancer research.
Research program of Dr. Przybyl aims to resolve diagnostic and therapeutic challenges in the treatment of patients with soft tissue tumors through development of novel clinically applicable liquid biopsy (circulating tumor DNA) assays.

Research program of Dr. Leung aims to detect biomarkers relevant to the screening and treatment of cervical cancer through liquid biopsy (circulating tumor DNA) and other protein biomarkers.

General Duties
Under the supervision of Dr. Przybyl and Dr. Leung, the clinical research coordinator will be responsible for supporting the successful conduct of oncology clinical research studies.

**SPECIFIC RESPONSIBILITIES**:

- Assess patients for protocol eligibility through personal interviews and/or medical record review in in-patient and out-patient settings,
- Pre-screen study participants,
- Obtain informed consent and recruit participants in clinic - explain the study and answer questions in English and French,
- Collect and store questionnaires, consent forms and participants’ study files,
- Coordinate biological specimen collection and organize their transfer to the analysis site,
- Act as the direct link between the investigators, the research teams and collaborating laboratories/co-investigators,
- Process collected samples according to standard operating procedures (SOPs) and store in standard and automated biobank systems,
- Administer and record answers for patient questionnaires,
- Perform data entry into clinical database,
- Ensure study related documents are completed in a timely manner, and documents are saved and filed,Maintain screening and enrollment logs,
- Retrieve clinical information from medical charts and electronic records and enter specific information into biobank data systems,
- Maintain, complete and update concomitant and adverse event logs,
- Assist with ethic submissions and amendments,
- Prepare reports on completed tasks,
- Communicate with Principal Investigators on a regular basis, and perform any other related tasks assigned by the Principal Investigators,
- Being certified to collect blood (venipuncture) and/or bodily fluid and other biological samples from patients who have provided informed consent for biobanking will be an asset.

**STANDARDS OF PERFORMANCE**:

- Demonstrates good listening, good interpersonal and communication skills,
- Respects policies and procedures,
- Takes initiative and is resourceful,
- Ability to multitask,
- Responds to others in a professional and courteous manner,
- Demonstrates attention to detail,
- Ability to display a high degree of discretion in dealing with confidential information.

Website of the organization

Education / Experience

**Education**: Diploma of College Studies (DEC)
- Minimum DEC in Nursing Science or Medical Technology or related field.

**Work Experience**:

- Minimum four (4) years of nursing experience or experience in a similar position, including two (2) years in a hospital setting.

**Professional Membership**: ? Yes ? No

**Other requirements**:

- Bilingual: French and English spoken and written,
- Solid written and verbal communication skills,
- Able to work under mínimal supervision,
- Self-directed, flexible, organized and sense of ethics,
- Experience in hematology and/or oncology is preferred,
- Clinical research experience is an asset,
- Knowledge of Microsoft Office (Word, Excel, Power Point and Outlook) is an asset.

Additional information

**Status**: Temporary, full time (35-hour workweek)

**Pay Scale**: Commensurate with education and experience

**Work Shift**: from 8:30 a.m. to 4:30 p.m., Mondays to Fridays

**Work Site**: : Glen

THIS IS NOT A HOSPITAL POSITION.

**NOTE**: The masculine gender has been used for brevity and includes the feminine gender.
Equal Opportunity Employment Program

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