Clinical Research Coordinator - Burnaby, Canada - Qu Biologics

Qu Biologics
Qu Biologics
Verified Company
Burnaby, Canada

2 weeks ago

Sophia Lee

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Sophia Lee

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Description

TITLE
Clinical Research Coordinator


TERMS OF EMPLOYMENT
This is a full-time, on-site position (1.0 FTE)


COMPANY PROFILE


Qu Biologics is a private, Phase 2 clinical-stage biopharmaceutical company located in Burnaby, BC developing Site Specific Immunomodulators (SSIs), a novel immunotherapy platform designed to restore normal immune function to reverse the chronic inflammation underlying many conditions including cancer and chronic inflammatory diseases.


IS QU FOR YOU?
Do you love doing something that you can feel passionate about? Are you excited by innovation, new ideas, and working with a creative, fun, and inspired team? Then, this is for you We'd love to hear from you if:

  • You are well-organized, understand the importance of detail, and can multi-task and prioritize duties effectively
  • You understand the importance of identifying and overcoming ratelimiting steps to ensure that projects are moving forward as quickly as possible, without sacrificing quality
  • You are innovative, practical, and enjoy finding the most efficient and costeffective solutions to realworld problems
  • You value respectful, open communication, and inspired teamwork to achieve shared goals
  • You always ask 'Why?'
The Clinical Research Coordinator reports to the Clinical Trial Manager.

Specific duties and responsibilities include but are not limited to:

  • Setting up and maintaining the trial site to comply with Regulatory, ICH-GCP and SOP requirements
  • Monitoring enrollment, identifying and problemsolving recruitment and/or other challenges in trial conduct
  • Ensuring protocol adherence and quality in trial conduct including risk mitigation
  • Attending meetings, assisting with creating and implementing strategies to meet study objectives and timelines
  • Participating in trial monitoring visits and attending to any followup items
  • Communicating clearly, concisely, professionally and in a timely fashion, at all times
  • Other related duties, as necessary

REQUIRED QUALIFICATIONS

  • Undergraduate degree or higher, in healthrelated discipline
  • SoCRA or ACRP certification preferred
  • TCPS2, GCP, Health Canada Division 5 and Transportation of Dangerous Goods training preferred
  • Experience working with clinical trials involving older adults an asset
  • At least 2 years coordinating clinical trials
  • Knowledge of all aspects of clinical trial coordination from study startup to closeout
  • Competency with computers and videoconferencing (Outlook, Word, Excel, Zoom)
  • Excellent interpersonal, oral, and written communication skills
  • Ability to working independently and collaboratively
  • Excellent organizational skills and attention to detail
  • Ability to think critically and prioritize workload to meet deadlines

LANGUAGE REQUIREMENTS
Fluent English


DESIRED START DATE
As soon as possible


COMPENSATION
Salary commensurate with experience ($58,000-$70,000 annually). Three (3) weeks annual vacation.


COMPANY & LOCATION OF WORK
Qu Biologics Inc.

4475 Wayburne Drive, Suite 305

Burnaby, British Columbia

V5G 4X4 Canada

**HOW TO APPLY
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