Job Title

Were partnered with a global clinical research organization that is transforming how healthcare and clinical trials reach underserved communities. With a growing presence across Canada and internationally, our partner delivers world-class research and health services directly to patientshelping advance medical breakthroughs while improving access to care.We are currently supporting them in the search for a Clinical Research Coordinator (Registered Nurse) to join their Cape Breton team.The OpportunityIn this role, youll support and coordinate clinical research studies while delivering hands-on patient care. Working closely with Investigators, Sponsors, and research teams, youll ensure trials are conducted in compliance with Good Clinical Practice (GCP), Health Canada regulations, and approved protocols - while maintaining a positive, patient-first experience.This is an ideal opportunity for an RN with strong clinical skills and an interest in research to make a meaningful impact beyond traditional bedside care.Key ResponsibilitiesStudy & Site CoordinationReview study protocols and amendments for feasibility and clarityEnsure all study training and requirements are completed prior to trial startCoordinate site initiation, monitoring, and investigator visitsSupport recruitment planning and participant outreachMaintain compliance with ICH-GCP and Health Canada Division 5 regulationsPatient Coordination & Clinical DutiesPrescreen and recruit study participantsObtain informed consent per SOPsConduct protocol-required visits and proceduresPerform phlebotomy, IV insertions, ECGs, vitals, and other delegated proceduresAdminister investigational products and monitor participants for adverse reactionsIdentify and report AEs and SAEs promptlyDocumentation & Regulatory SupportMaintain accurate, real-time source documentation (paper or e-source)Manage study drug accountability and inventoryResolve data queries within sponsor timelinesAssist with regulatory documentation and filingsRN-Specific ResponsibilitiesPreparation, administration, storage, and accountability of investigational productsMaintain product blinding where applicableEnsure proper storage conditions and temperature monitoringMaintain RN licensure and required research trainingWhat Were Looking ForRequiredActive Registered Nurse (RN) license in good standing (Nova Scotia)Minimum 1 year of relevant clinical research experienceStrong phlebotomy and infusion skillsExcellent communication and organizational skillsAbility to work independently in a fast-paced environmentWorking knowledge of GCP and federal research regulationsYoull also bring a collaborative mindset, strong attention to detail, and a genuine interest in contributing to medical innovation.Location & Work EnvironmentOn-site role in Cape Breton, Nova ScotiaRegular use of computer systems and clinical equipmentCompensation & Benefits6 weeks paid vacation annuallyA competitive base salaryComprehensive group health benefits (including dependents)Voluntary group RRSP with employer matchingOpportunity to be part of a rapidly growing global CRO, contributing to research that improves access to healthcare and advances future medicine