Clinical Research Coordinator

3 weeks ago

Vancouver, Canada Vancouver Infectious Diseases Centre (VIDC) Full time

Clinic Description:
The Vancouver Infectious Diseases Centre (VIDC) is a medical and research centre that uses a multidisciplinary care model for the delivery of specialty health care providing expert, state-of-the art diagnosis and treatment of chronic infectious diseases and related conditions (including addiction and pain management), with a focus on HIV and HCV infections. VIDC particularly seeks to engage more vulnerable patients in a multi-disciplinary environment of health care. We provide peer-friendly education about disease, state-of-the-art antiviral medications and comprehensive support during and after treatment within an open, flexible and community-based holistic approach. Services are provided in English and French.

Job Responsibilities and Description:
Clinical Trial/ Clinical Research:

- Maintaining screening logs, enrolment logs and study related source documentation
- Informed consent process as per guideline
- Development and maintenance of trial specific paperwork/source documents
- Ensuring laboratory and other medical reports are reviewed and evaluated by either the PI or one of the sub-Is
- Reporting adverse/ serious adverse events to PI and trial sponsor
- Updating recruitment data
- Attending research/investigator meetings
- Updating other research staff regarding the progress of clinical trials
- Completion of Case Report Forms (CRFs) and Data Query/ Clarification Forms (DQ/|CFs)
- Storage of study related supplies within a locked secure placement
- Storage of study medications and documentation of study drug accountability and reconciliation
- Ongoing communication with Sponsor and prompt response to any study related information required by the Sponsor
- Participating in Interim Monitoring Visits (IMV) with the Clinical Trial Monitor and responding to study related queries within timely fashion
- Maintaining IATA dangerous good shipment certification
- Shipping laboratory samples to appropriate laboratories in accordance to IATA dangerous good shipment procedures
- Ensuring that GCP training is up to date
- Maintaining trial specific paperwork by regular filing of trial related documents
- Ensuring that all laboratory materials such as lab kits, requisitions and shipping supplies are kept in sufficient supply

**Job Types**: Full-time, Contract

**Salary**: $45,000.00-$65,000.00 per year

**Benefits**:

- Dental care
- Extended health care

Schedule:

- Monday to Friday

**Education**:

- Bachelor's Degree (preferred)

**Experience**:

- Clinical Research Coordinators: 1 year (preferred)

Work Location: In person

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