QuBiologics: Clinical Research Coordinator

Closed
Open until filled
Yes
Closing date
Internal / External
External to BC AHSN
Job type
Full time
Location
Fraser Health Region
How to apply

If this opportunity matches your character, experience, and skill set, please email a cover letter and curriculum vitae in PDF format, to jobs@qubiologics.com with the job code: ‘Clinical Research Coordinator’ in the header. Applications will not be accepted by fax, mail, or over the phone.

While we thank all applicants for their interest, only short-listed candidates will be contacted. Please note that we will not be fielding inquires by phone

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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 rate-limiting 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 cost-effective solutions to real-world problems
  • You value respectful, open communication, and inspired teamwork to achieve shared goals
  • You always ask ‘Why?’

POSITION DESCRIPTION

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 requirements
  • Performing and/or supporting day-to day activities from study start-up to study close-out including enrollment, lab sampling, processing and/or shipping, Investigational Product management, data management, safety reporting, maintenance of Regulatory and training documentation, ethics applications, study document archiving
  • Monitoring enrollment, identifying and problem-solving 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 follow-up 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 health-related 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 5 years coordinating clinical trials
  • Knowledge of all aspects of clinical trial coordination from study start-up to close-out
  • 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. Three (3) weeks annual vacation.

COMPANY & LOCATION OF WORK

Qu Biologics Inc. 4475 Wayburne Drive, Suite 305 Burnaby, British Columbia V5G 4X4 Canada