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$55k–$63k/yr
Full-time
bachelor degree
Incentive compensation
Posted 14d ago
~40 hrs/week
Responsibilities
The Clinical Research Coordinator will independently manage clinical study activities, including participant visits, phlebotomy, and regulatory compliance. They will also collaborate with investigators and the research team to ensure data integrity and participant safety throughout the study lifecycle.
Requirements
Candidates must hold a bachelor's degree in a health, science, or research-related field and possess at least 3 years of clinical research experience. Additionally, they must have 3 years of hands-on phlebotomy experience and be currently qualified to perform phlebotomy in Canada.
Full job description
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.
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
Offices: 910 Talbotton Rd, Columbus, Georgia 31904, US · 1929 Bayview Ave, 106, Toronto, Ontario M4G 3E8, CA
Clinical ResearchPrimary CarePhase I to IVDrug DevelopmentClinical TrialsClinical Studiesand BiotechnologyService IndustryConsultingBiotechnology
How many Administrative jobs are open in Vaughan, Canada right now?
There are currently 168 open administrative positions in Vaughan, Canada listed on Clera. New openings are added daily as companies post roles.
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Companies currently hiring include AWIN Group of Dealerships, Global Elite Consultants, OZZ Group, Clearway Construction, VetStrategy, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Administrative jobs in Vaughan, Canada?
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