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 Opportunity In 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 Responsibilities Study & Site Coordination Review study protocols and amendments for feasibility and clarity Ensure all study training and requirements are completed prior to trial start Coordinate site initiation, monitoring, and investigator visits Support recruitment planning and participant outreach Maintain compliance with ICH-GCP and Health Canada Division 5 regulations Patient Coordination & Clinical Duties Prescreen and recruit study participants Obtain informed consent per SOPs Conduct protocol-required visits and procedures Perform phlebotomy, IV insertions, ECGs, vitals, and other delegated procedures Administer investigational products and monitor participants for adverse reactions Identify and report AEs and SAEs promptly Documentation & Regulatory Support Maintain accurate, real-time source documentation (paper or e-source) Manage study drug accountability and inventory Resolve data queries within sponsor timelines Assist with regulatory documentation and filings RN-Specific Responsibilities Preparation, administration, storage, and accountability of investigational products Maintain product blinding where applicable Ensure proper storage conditions and temperature monitoring Maintain RN licensure and required research training What Were Looking For Required Active Registered Nurse (RN) license in good standing (Nova Scotia) Minimum 1 year of relevant clinical research experience Strong phlebotomy and infusion skills Excellent communication and organizational skills Ability to work independently in a fast-paced environment Working knowledge of GCP and federal research regulations Youll also bring a collaborative mindset, strong attention to detail, and a genuine interest in contributing to medical innovation. Location & Work Environment On-site role in Cape Breton, Nova Scotia Regular use of computer systems and clinical equipment Compensation & Benefits 6 weeks paid vacation annually A competitive base salary Comprehensive group health benefits (including dependents) Voluntary group RRSP with employer matching Opportunity to be part of a rapidly growing global CRO , contributing to research that improves access to healthcare and advances future medicine