Job Description

Jewish General Hospital (Lady Davis Institute)

Clinical Research Unit of Radiation-Oncology

Working under the direction of the Principal Investigator (PI), the clinical research coordinator is responsible for supporting the successful conduct of clinical research studies in the radiation-oncology department. The focus of the clinical research involves prostate cancer.

Key responsibilities and duties:

Conduct and participate in the informed consent process, including interacting with the research participants, answering any questions related to the study, and obtaining appropriate signatures on informed consent forms. Screen subjects for eligibility using protocol-specific inclusion and exclusion criteria. Register participants to the appropriate coordinating centre (if multi-site study). Coordinate participant tests and procedures on-site within a multidisciplinary team and coordinate with study teams of other participating centres (for multi-site studies). Collect data, completing case report forms, and answering queries in an accurate and timely manner as required by the protocol in order to maintain study timelines. This involves monitoring the data entry of other participating centres (for multi-site studies). Collaborate with the PI and Trials Manager to prepare ethics and regulatory submission documents to Research Ethics Board and Health Canada for new and ongoing trials. Prepare other study materials as requested by the PI. These study materials include, but are not limited to protocol, informed consent forms, case report forms, enrollment logs, and standard operating procedures. Organise and create study files, including but not limited to, regulatory binders, study specific source documentation and other materials. Prepare, centrifuge, and ship participant blood samples as per protocol lab manual. Assist PI in abstract and manuscript writing.

This is a 3-year contract after completion of a 3-month probation period. Renewable based on performance.

Benefits:

Extended health, dental and vision benefits with Blue Cross after completion of a 3-month probation period. 13 statutory holidays/year 9.6 sick days/year (after 3 months of employment) 20 vacation days/year (after 1 year of employment)
Job Type: Full-time (35 hours/week), on-site.

Salary: $22-$33 per hour

Requirements:

Bilingual: English/French (oral and written) Bachelor's Degree (in related field preferred) or previous research experience Highly motivated, organized and good time-management Excellent communication skills(with research participants and multidisciplinary team) Computer skills(Word, Excel)
Job Type: Full-time

Pay: $22.62-$33.65 per hour

Benefits:

Dental care Extended health care Vision care
Ability to commute/relocate:

Montreal, QC H3T 1E2: reliably commute or plan to relocate before starting work (required)
Education:

Bachelor's Degree (required)
Language:

French (required) English (required)
Work Location: In person