Clinical Research Coordinator - Vancouver, Canada - Vancouver Infectious Diseases Centre (VIDC)

Vancouver Infectious Diseases Centre (VIDC)

Verified Company

Vancouver, Canada

3 days ago

Posted by:

Sophia Lee

beBee Recruiter

Description

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 subIs
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