Clinical Trials Coordinator

6 months ago

Vancouver, Canada Vancouver Prostate Centre Full time

Clinical Trials Coordinator

The Vancouver Prostate Centre (VPC) has an exceptional opportunity available for a **temporary, full-time Clinical Trials Coordinator**, with an opportunity of extension to permanent full-time based on performance.
**VPC Salary Range**: Professional and Technical Staff, Level 5: $46, 804 - $67, 282 per annum
**Reports to**: PI and Clinical Trials Manager

**The Vancouver Prostate Centre**
**Clinical Trials Coordinator**

**Responsibilities**
Coordinate Phase 1-1V clinical trials; process regulatory documentation; complete case report forms; resolve data queries; recruit/screen patients according to protocol; schedule patient study visits and tests; process and ship study specimens; coordinate sponsor visits; participate in audits; assist with processing safety reports; and attend investigator initiation meetings. Key duties include:

- Manage recruitment, screening, enrollment and data collection of study participants, ensuring protocol compliance.
- Coordinate and manage patient study visits and tests.
- Responsible for data and source documentation, as well as adverse event reporting.
- Process and ship study specimens.
- Schedule and conduct study initiation, monitoring and close-out visits with sponsors, Clinical Research Organizations and other applicable parties.
- Participate in the conduct of audits by study sponsors, Clinical Research Organizations, Heath Canada and Food and Drug Administration and other entities as required.

**Decision Making/Level of Accountability/Extent of Authority**
Significant

**Supervision Received**
Minimal.

**Supervision Given**
None
**Qualifications and Experience**
- Baccalaureate Degree in a health-related science.
- Three years of related professional experience such as coordinating clinical trials.
- Laboratory experience or willing to train on protocols to process blood and urine samples.
- Phlebotomy experience or willing to train on Phlebotomy.
- Experience with case report form creation and completion.
- Experience with electronic data capture platforms and ability to resolve data queries.
- Excellent organization and communication skills with ability to effectively communicate and provide support to investigators and patients.
- Demonstrated meticulous attention to detail
- Solid computer expertise.
- Able to work independently and as part of a team, with mínimal supervision.
- Proven decision-making and effective time management.

**Application Procedures**
- Cover letter
- Resume

**Job Types**: Full-time, Fixed term contract
Contract length: 12 months

Pay: $46,804.00-$67,282.00 per year

**Benefits**:

- Dental care
- Extended health care
- Paid time off

Schedule:

- Monday to Friday

**Education**:

- Bachelor's Degree (preferred)

Work Location: In person

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