Clinical Research Coordinator

7 days ago

Burnaby, Canada Qu Biologics Full time

**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?’

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 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 2 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 ($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

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