Clinical Research Coordinator

We’re 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 patients—helping 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, you’ll support and coordinate clinical research studies while delivering hands-on patient care. Working closely with Investigators, Sponsors, and research teams, you’ll 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 We’re 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

You’ll 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