Clinical Research Coordinator

Vancouver Infectious Diseases Centre (VIDC) - Vancouver, BC (18 days ago)

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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:

VIDC is seeking a dynamic individual to support our patient engagement initiatives in a multidisciplinary medical and research centre. A great candidate will be enthusiastic, self-motivated and confident to work in an energetic and a compassionate team.

Clinical Trial/ Clinical Research:

  • Screening and recruitment of subjects
  • Maintaining screening logs, enrollment logs and study related source documentation
  • Informed consent process as per guideline
  • Supporting of subject and significant others
  • Maintaining study subject binders
  • Development and maintenance of trial specific paperwork/source documents
  • Planning and booking subject’s protocol-related tests/ investigations/ appointments as required
  • Performing subject visits and all study related procedures following the specific protocol of the trial
  • 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
  • Assisting subjects with study specific visits, arranging meals and scheduling appointments with healthcare providers for MRI, CT scans etc.
  • Liaising/communicating with trial sponsors, subjects, health-care providers etc.
  • Ensuring that all laboratory materials such as lab kits, requisitions and shipping supplies are kept in sufficient supply

Job Type: Full-time

Experience:

  • Clinical Research: 2 years (Required)

Education:

  • Bachelor's Degree (Required)