Join Us at Centricity Research!
Centricity Research is one of the largest clinical research networks in North America. We are a fully centralized Integrated Research Organization (IRO) specializing in conducting Phase I-IV clinical trials in over 35 therapeutic areas: inpatient and outpatient; pharmaceutical, biotechnology, and medical device trials.
About the role
We are seeking an experienced, full-time, permanent Clinical Research Coordinator (CRC) to join our ON-VAU/Vaughan site. 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 position is primarily based at Centricity Research Vaughan Endocrinology site in Vaughan and will also provide support to Centricity Research Toronto LMC Multispecialty and Centricity Research CPU-Toronto sites as operational needs require.
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 at least 3 years of 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.
- Are willing and able to work primarily at Centricity Research Vaughan Endocrinology site in Vaughan and provide support to Centricity Research Toronto LMC Multispecialty and Centricity Research CPU-Toronto sites as operational needs require.
Skills Required
- Bachelor's degree in a health, science, or research-related field or equivalent combination of education and experience
- At least 3 years of clinical research experience coordinating studies and conducting participant visits
- At least 3 years of hands-on phlebotomy experience and currently qualified to perform phlebotomy in Canada
- Strong knowledge of medical terminology, Good Clinical Practice (GCP), study protocols, SOPs, and clinical research documentation requirements
- Experience performing clinical procedures: vitals, ECGs, sample collection/processing, investigational product handling
- Experience with recruitment, screening, informed consent, scheduling, and enrollment processes
- Experience supporting monitoring visits, audits, inspections, and performing data/source QC checks
- Ability to work primarily at Centricity Research Vaughan site and provide support to Toronto sites as operational needs require
- Organized, detail-oriented, able to prioritize multiple responsibilities and work independently
- Experience across multiple therapeutic areas (vaccines, obesity, rare diseases, Alzheimer’s) considered an asset
What We Do
Centricity Research is an integrated research organization (IRO) with more than 40 wholly owned and integrated clinical research offices across North America. The company conducts Phase I-IV clinical research in over 35 therapeutic areas: inpatient and outpatient; pharmaceutical, biotechnology, and medical device trials. For more than 25 years, the organization’s founders have worked to revolutionize research by investing in the people and technology needed to deliver outstanding clinical trial experiences, earning numerous awards including “Best Places to Work” and recognition for “Outstanding Diversity in Clinical Research.” Jobseekers: Apply here >> https://centricityresearch.applytojob.com/apply
