Clinical Research Coordinator

Job summary

The Clinical Research Coordinator will independently manage clinical study activities, including participant visits, phlebotomy, and protocol compliance. They will also support recruitment, data integrity, and site-level regulatory documentation to ensure participant safety.

Job details

About the role We are seeking an experienced, full-time, permanent Clinical Research Coordinator (CRC) to join our new Centricity Research Toronto LMC Multispecialty site team. In this role, you will independently coordinate clinical studies, conduct participant visits and phlebotomy, and work closely with Investigators and the broader research team to ensure study activities are safe, organized, accurate, and compliant with protocol and regulatory requirements. This role is ideal for a proactive coordinator who can take ownership, adapt quickly, and contribute immediately in a growing team environment. Compensation Base salary range: $55,000-$62,500. This role is eligible for incentive compensation. What you'll do Study Coordination & Participant Safety Conduct study visits in accordance with protocol, GCP, SOPs, and regulatory requirements Ensure participant safety and well-being, reporting and documenting adverse events per protocol and regulations Perform clinical procedures such as vitals, ECGs, sample collection/processing, and investigational product handling Recruitment, Screening & Enrollment Support recruitment strategies to identify and enroll eligible participants Conduct participant screening according to protocol inclusion/exclusion criteria Guide participants through the informed consent process and ensure proper documentation Schedule and coordinate study visits throughout the participant lifecycle Study Execution & Data Integrity Accurately complete study documentation, regulatory records, and periodic reports Prepare for and support monitoring visits, audits, and inspections Perform regular quality control (QC) checks on study data and source documents Collaborate with investigators, management, and sponsors to ensure study compliance and accuracy Contribute to site start-up activities, including feasibility questionnaires (FQs) and pre-study visits (PSVs) Quality, Compliance & Site Support Support lab supply inventory, equipment maintenance, and administrative needs Assist with community engagement and outreach events as needed You Might Be a Great Fit If You: Have a bachelor's degree in a health, science, or research-related field, or an equivalent combination of relevant education and experience. Have at least 3 years of clinical research experience, including demonstrated experience coordinating studies and conducting participant visits. Have hands-on phlebotomy experience and are currently qualified to perform phlebotomy in Canada. Have strong knowledge of medical terminology, GCP, study protocols, SOPs, and clinical research documentation requirements. Experience across multiple therapeutic areas, such as vaccines, obesity, rare diseases, or Alzheimer's disease, is considered an asset. Are organized, detail-oriented, and skilled at prioritizing multiple responsibilities in a fast-paced environment. Are a self-starter who can work independently, take ownership of assigned studies, and become productive quickly with limited supervision. Communicate openly, collaborate effectively, and contribute positively to a new and growing site team.

What you’ll do

The Clinical Research Coordinator will independently manage clinical study activities, including participant visits, phlebotomy, and protocol compliance. They will also support recruitment, data integrity, and site-level regulatory documentation to ensure participant safety.

Requirements

Candidates must hold a bachelor's degree in a health or science-related field and possess at least 3 years of clinical research experience. Hands-on phlebotomy qualification and strong knowledge of GCP and medical terminology are required.

Benefits

• Incentive compensation

Listed skills

• Control · Preferred
• Recruitment · Preferred
• Organized · Preferred
• Health · Preferred
• Detail-oriented · Preferred
• Compliance · Preferred
• safety · Preferred
• Documentation · Preferred
• Accuracy · Preferred
• Administrative · Preferred
• Google Cloud · Preferred
• coordination · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

• Clinical research coordination
• Phlebotomy
• Participant screening
• Informed consent
• GCP compliance
• Regulatory documentation
• Adverse event reporting
• ECG
• Vitals monitoring
• Data integrity
• Quality control
• Study protocol management
• Medical terminology
• Site start-up
• Participant recruitment
• Informed Consent
• Supply Inventory
• Self-Starter
• Equipment Maintenance
• Vital Signs
• Recruitment Strategies
• Research
• Auditing
• Management
• Clinical Research
• Clinical Research Coordination
• Clinical Trials
• Data Integrity
• Health Sciences
• Medical Terminology
• Sample Collection
• Coordinating
• Quality Control
• Detail Oriented

Job areas

• Healthcare
• Science & Research
• Clinical Research Coordinator
• Research and Development Managers
• Clinical Research Coordinators
• Natural Sciences Managers