GCP Consultant / GCP Auditor (Clinical Research)
- Canada (Remote / Hybrid Options Available)
- Company: Conduct Research
- Employment Type: Contract / Full-Time
Company Description
Conduct Research is a Canada-based Clinical Research Organization (CRO).
We support sponsors and research sites with end-to-end clinical trial execution, ensuring compliance, efficiency, and data integrity across all phases. Our unique rural site network provides expanded patient access and improved recruitment outcomes for sponsors.
As we continue to grow, we are seeking an experienced GCP Consultant / Auditor to support our quality and compliance initiatives.
Job Description
The GCP Consultant / GCP Auditor will play a critical role in ensuring that clinical trials are conducted in compliance with ICH-GCP guidelines, regulatory requirements, and internal SOPs.
You will lead and support audits, inspections, and quality assurance processes, working closely with sponsors, sites, and internal teams.
Key Responsibilities
- Conduct GCP audits (site, vendor, internal, and system audits)
- Ensure compliance with ICH-GCP, Health Canada, and global regulatory requirements
- Review clinical trial documentation, TMFs, and study processes
- Identify compliance gaps and provide corrective and preventive actions (CAPA)
- Support inspection readiness and regulatory submissions
- Develop and maintain quality management systems (QMS) and SOPs
- Provide training and guidance to research staff on GCP standards
- Collaborate with sponsors and stakeholders to ensure audit readiness and quality oversight
Qualifications
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or related field
- Minimum 3–5+ years of experience in clinical research, QA, or auditing
- Strong knowledge of ICH-GCP, Health Canada regulations, and clinical trial processes
- Experience conducting GCP audits and inspections
- Familiarity with TMF review, monitoring, and site management
- Excellent analytical, documentation, and communication skills
Preferred Qualifications
- Certification in GCP / Clinical Research / Quality Assurance
- Experience with CROs, SMOs, or sponsor-side auditing
- Experience with risk-based monitoring and remote audits
What We Offer
- Opportunity to work with a growing CRO in Canada
- Exposure to diverse clinical trials and therapeutic areas
- Flexible work environment (remote / hybrid)
- Competitive compensation package
- Career growth in clinical quality and compliance leadership
Why Join Conduct Research
- Strong expertise in clinical trial execution
- Access to rural patient populations (unique sponsor advantage)
- Focus on quality, compliance, and operational excellence
- Collaborative and innovation-driven culture
How to Apply
📧 Email your CV to: clinicaltrials@conductresearch.ca