Careers at Conduct Research Inc
Shape the Future of Clinical Research
"Every trial we run is a real patient waiting for an answer."
At Conduct Research Inc., we don't just manage clinical trials — we build the systems, teams, and trust that bring life-changing therapies from hypothesis to approval.
Our Edmonton-based team works alongside sponsors, sites, and regulators across Canada and beyond.
Through our sister company MD Trials, we offer access to an established site network that gives our team unmatched proximity to trial sites and patients.
That connection fuels everything we do.
Join a quality-first CRO where your expertise drives real clinical outcomes - from oncology to infectious disease, Phase I through IV.
More Than a CRO —
A Community of Committed Scientists
Quality-First Culture
GCP and GMP compliance aren't checkboxes here — they're the foundation of every decision we make.
Real Regulatory Exposure
Work across FDA, Health Canada, and ICH-GCP frameworks on live studies with global impact.
Career Growth Paths
From CRA to QA leadership — we invest in your professional development as our portfolio grows.
Collaborative Site Network
Conduct Research Inc. gives you direct access to sites and investigators — rare in a CRO environment.
Open Positions
Current Opportunities
GCP / GMP Auditor (Clinical Research & Quality Assurance)
Location: Canada (Remote / Hybrid)
Type: Full-Time / Contract
Overview : The GCP/GMP Auditor ensures compliance with ICH-GCP and GMP standards by conducting audits, identifying risks, driving CAPA, and supporting regulatory inspection readiness across clinical trials and quality systems.
About Conduct Research : Conduct Research Inc. is a Canada-based CRO focused on clinical trial execution, GCP compliance and auditing, patient recruitment and retention, and regulatory and quality systems. We help sponsors and sites run high-quality, compliant, and successful clinical trials.
Your Role : As a GCP/GMP Auditor, you will build and maintain a strong compliance framework across clinical operations and quality systems, working closely with clinical trial sites, sponsors and CRO partners, and our internal QA and regulatory teams. Your work will directly affect data integrity, patient safety, and regulatory approvals.
Key Responsibilities
- Conduct GCP and GMP audits (site, vendor, internal, and system)
- Evaluate compliance with ICH-GCP, GMP, FDA, and Health Canada requirements
- Review Trial Master Files, SOPs, validation reports, and batch records
- Identify risks and drive Corrective and Preventive Actions (CAPA) to closure
- Support inspection readiness and regulatory audits
- Develop and improve Quality Management Systems
- Prepare detailed audit reports and compliance documentation
- Train teams on GCP/GMP best practices and regulatory expectations
What You Bring
- Degree in life sciences, pharmacy, biotechnology, or a related field
- 3–7+ years in QA, auditing, or clinical research
- Strong working knowledge of ICH-GCP, GMP, and applicable regulatory frameworks
- Hands-on experience with GCP/GMP audits and inspections
- Excellent documentation and analytical skills
Preferred
- Certification in GCP, QA, or clinical research
- CRO, SMO, or sponsor-side auditing experience
- Exposure to oncology, infectious disease, or medical device trials
- Experience with risk-based auditing and remote inspections
How You'll Succeed
- Strong attention to detail and a compliance mindset
- Ability to manage multiple audits and deadlines
- Clear, professional reporting and communication
- Proactive risk identification and resolution
Why Join Conduct Research
- Work on real clinical trials with measurable impact
- Gain exposure to global regulatory environments
- Join a quality-first CRO
- Grow into QA and regulatory affairs leadership
Application Process Submit application → initial screening → technical evaluation → final interview → offer
How to Apply Email your CV to clinicaltrials@conductresearch.ca
Clinical Trial Project Manager (Oncology)
Location: Remote (Canada preferred; North America considered)
Employment Type: Part-Time (with potential to transition to full-time)
Company: Conduct Research Inc.
About Us : Conduct Research Inc. is a growing Contract Research Organization (CRO) dedicated to delivering high-quality clinical trial management services. We partner with biotechnology and pharmaceutical companies to support early- and late-phase clinical trials with a strong emphasis on quality, compliance, and operational excellence.
We are seeking an experienced Clinical Trial Project Manager with a strong background in oncology clinical trials to lead and coordinate sponsor-funded studies from study start-up through closeout.
Position Summary : The Clinical Trial Project Manager will oversee the operational execution of assigned oncology studies while serving as the primary point of contact for sponsors, sites, vendors, and internal team members. The successful candidate will have demonstrated experience managing complex oncology clinical trials within a CRO, sponsor, or academic research environment.
Key Responsibilities
Lead day-to-day management of assigned oncology clinical trials.
Serve as the primary liaison between sponsors, investigators, vendors, and study teams.
Develop and maintain project plans, timelines, study trackers, and risk management plans.
Monitor study milestones, enrollment, site performance, and overall project health.
Coordinate study start-up activities, including site activation and vendor management.
Lead project meetings and prepare meeting agendas, minutes, and action items.
Ensure compliance with study protocols, ICH-GCP, SOPs, and applicable regulatory requirements.
Identify project risks and implement mitigation strategies.
Review monitoring reports, protocol deviations, CAPAs, and study metrics.
Collaborate with Clinical Research Associates, Regulatory, Data Management, Safety, and Quality teams.
Support budget tracking, change orders, invoicing, and financial forecasting.
Assist with sponsor audits and regulatory inspections as required.
Required Qualifications
Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or a related healthcare discipline.
Minimum 5 years of clinical research experience.
Minimum 3 years of project management experience leading clinical trials.
Demonstrated experience managing oncology clinical trials is required.
Experience working within a CRO environment is strongly preferred.
Thorough knowledge of ICH-GCP, FDA, Health Canada, and applicable regulatory requirements.
Strong understanding of study start-up, site management, monitoring, data management, and closeout activities.
Excellent organizational, communication, and leadership skills.
Ability to independently manage multiple projects in a remote environment.
Preferred Qualifications
Experience with Phase I–III oncology studies.
Experience with investigator-sponsored trials and biotech sponsors.
Familiarity with CTMS, eTMF, EDC, and Microsoft Office applications.
PMP certification or equivalent project management training is considered an asset.
Experience managing international or multicenter studies is an asset.
What We Offer
Fully remote work environment.
Flexible part-time schedule.
Opportunity to work with innovative biotechnology sponsors.
Collaborative, quality-focused team culture.
Opportunity for growth as the company expands.
What to submit
Please submit the following:
Resume/CV
Cover Letter highlighting your oncology project management experience
Expected hourly rate or salary expectations
Earliest available start date
Only candidates with demonstrated oncology clinical trial project management experience will be contacted for interviews.
Application Process Submit application → initial screening → technical evaluation → final interview → offer
How to Apply Email your CV to clinicaltrials@conductresearch.ca
Ready to Apply?
Send your CV and a brief cover letter to our clinical trials team. We review every application personally.