Regional Research Assistant (RA) – GTA

Résumé du poste

The Regional Research Assistant supports clinical research studies by performing phlebotomy, conducting participant assessments, and ensuring protocol compliance across multiple sites. They are responsible for data integrity, maintaining source documents, and assisting with recruitment and site operations.

Détails du poste

About the role We’re looking for a Regional Research Assistant (RA) to support the successful execution of clinical research studies across our Etobicoke, Brampton, and Manna Toronto sites. Etobicoke will be the primary location, with regular travel to the other sites based on participant and study needs. You’ll work closely with Investigators, Clinical Research Coordinators (CRCs), and the wider site teams to ensure studies run smoothly, safely, and in full compliance with protocols and regulations. This hands-on role includes phlebotomy, participant follow-up visits, chart and data-query reviews, data entry, sample processing, and accurate study documentation. Site assignments will be planned with advance notice wherever possible. The regular schedule is Monday to Friday, generally 8:00 a.m.–4:00 p.m. or 8:30 a.m.–4:30 p.m What you'll do Study Protocol & Safety: Conduct study activities in compliance with GCP, SOPs, and protocols; monitor participant safety; and perform scheduled visits and assessments (e.g., vitals, ECGs). Recruitment & Enrollment: Support recruitment efforts, screen participants, obtain informed consent, and maintain accurate documentation. Study Visit Execution: Perform phlebotomy and blood collection as a core responsibility; support participant follow-up visits; and complete other delegated tasks such as sample collection/shipping, point-of-care testing, and investigational product accountability. Data Integrity & Compliance: Complete chart reviews and resolve data queries; maintain accurate source documents, CRFs, and CTMS records; report adverse events promptly; and support investigational product inventory and storage compliance. Site & Administrative Support: Support operations across Etobicoke, Brampton, and Manna Toronto; prepare for monitoring visits and audits; maintain ISF; organize exam rooms and labs; assist with scheduling, participant check-in/out, data entry, and outreach. Regular travel is required, though travel among all three sites in one day is not normally expected You Might Be a Great Fit If You: Have a degree in a health, science, or research-related field, or equivalent relevant experience supported by basic health and medical knowledge. Have phlebotomy training and demonstrated experience independently performing blood draws in a clinical, laboratory, or research setting. Hold a valid driver’s licence and have reliable transportation. Travel between sites is a core requirement, and employees are responsible for their transportation between work locations. Have experience in clinical research, healthcare, patient testing, or another relevant patient-facing environment. Communicate clearly and professionally with participants, colleagues, and external partners. Are tech-savvy and comfortable navigating Microsoft Office, clinical data systems, chart reviews, and data-query workflows. Thrive in a team environment while also working independently, staying organized, and adapting to changing priorities across multiple sites. Bring Hindi or Punjabi language skills—an asset for participant communication at the Brampton and Etobicoke sites, but not a requirement. Experience with follow-up visits, informed consent, ECGs, vital signs, point-of-care testing, or sample processing/shipping is also an asset. Why Centricity Research? Our Mission We connect people to scientific advancements through groundbreaking research within a deeply human experience. Our Core Values Quality: We aim for excellence and integrity in everything we do - because lives depend on it. Care: We show up for each other, our customers, and our mission - always going the extra mile. Be the Change You Seek: We're adaptable, forward-thinking, and constantly improving - for the betterment of all. One Team: We collaborate, support one another, and succeed together. Grow for Good: We grow with purpose - to expand access to research and improve global health. Own It: We take initiative, deliver results, and follow through - with passion and accountability. Benefits Comprehensive health, dental, and vision insurance Enhanced EAP – mental health support Flexible PTO + paid holidays Continuing education reimbursement 401(k) / RRSP with company match and immediate vesting Ready to Apply? We’d love to hear from you – apply now! We’re an equal opportunity employer committed to building a diverse and inclusive workplace. We welcome applicants from all backgrounds and will provide accommodations during the hiring process upon request.

Ce que vous ferez

The Regional Research Assistant supports clinical research studies by performing phlebotomy, conducting participant assessments, and ensuring protocol compliance across multiple sites. They are responsible for data integrity, maintaining source documents, and assisting with recruitment and site operations.

Exigences

Candidates must have a degree in a health, science, or research-related field and demonstrated experience in phlebotomy. A valid driver's license and reliable transportation are required for travel between clinical sites.

Avantages

• Health insurance • Dental insurance • Vision insurance • Mental health support • Flexible PTO • Paid holidays • Continuing education reimbursement • 401(k) / RRSP with company match

Compétences indiquées

• Microsoft Office · Souhaitée
• Saisie de données · Souhaitée
• Gestion des stocks · Souhaitée

Autres compétences pertinentes

Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.

• Phlebotomy
• Clinical research
• Participant recruitment
• Informed consent
• Data entry
• Chart review
• Sample processing
• Vitals assessment
• ECG
• Point-of-care testing
• GCP compliance
• SOP adherence
• Microsoft Office
• Clinical data systems
• Adverse event reporting
• Inventory management
• Informed Consent
• Administrative Support
• Workplace Inclusivity
• Accountability
• Workflow Management
• Vital Signs
• Follow Through
• Research
• Auditing
• Medical Science
• Mental Health
• Blood Donation Drives
• Medical Laboratory
• Clinical Research
• Clinical Trial Management Systems
• Communication
• Data Entry
• Data Integrity
• Employee Assistance Programs
• Health Sciences
• Operations
• Point-Of-Care Testing
• Proactivity
• Punjabi Language
• Sample Collection
• Scheduling
• Technical Acumen

Domaines d’emploi

• Science & Research
• Healthcare
• Administrative
• Grant Research Assistant
• Research Assistant
• Survey and Market Research Interviewers
• Physical Scientists, All Other