Research Assistant / Laboratory Specialist (Vaughan)
Research Assistant / Laboratory Specialist (Vaughan)
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Vaughan, Canada
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Publiée: il y a moins d’une semaine
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Description
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’re looking for a Research Assistant / Lab Specialist to support the successful execution of clinical research studies from start to finish. In this role, you’ll work closely with Investigators, Clinical Research Coordinators (CRCs), and the wider site team to ensure studies run smoothly, safely, and in full compliance with protocol and regulations. This hands‑on role is varied—some days you’ll recruit and screen participants, other days you’ll collect data, process samples, or keep study documentation organized and accurate.In addition to Research Assistant responsibilities, you will also perform routine laboratory sample collection, processing, and shipping in accordance with study protocols, laboratory manuals, SOPs, and company guidelines. Your work will directly contribute to advancing clinical research that makes a difference in patients’ lives.What You’ll Do
Support Study Protocol&Safety
Conduct study activities in compliance with GCP, SOPs, and study protocols. Monitor participant safety and well‑being throughout their study journey. Schedule and conduct study visits, including vitals, ECGs, and other protocol‑required assessments.
Sample Collection&Laboratory Procedures
Perform phlebotomy, sample collection, processing, and shipping as required by protocol. Complete requisition, labeling, storage, and shipment of specimens accurately. Conduct blood glucose testing for diabetes participants and other point‑of‑care testing (e.g., nasal swabs) as required. Perform ECGs, vital signs, meal distribution, and other clinical procedures as required by protocol/site.Perform PBMC collection, receipt of samples, isolation, and cryopreservation as required. Maintain PBMC supplies, documentation, and samples.
Recruitment, Screening&Enrollment
Assist with recruitment strategies and outreach efforts to identify eligible participants. Screen participants according to inclusion/exclusion criteria. Obtain informed consent and maintain accurate documentation.
Study Visit Execution
Perform delegated clinical tasks such as phlebotomy, sample collection and shipping, point‑of‑care testing, and investigational product accountability. Accurately complete source documents, CRFs, queries, and maintain CTMS records.
Data Integrity&Compliance
Collect and report adverse events promptly, including SAEs within required timelines. Maintain investigational product inventory, logs, and storage conditions. Conduct quality control checks to ensure data accuracy and protocol compliance.
Site&Administrative Support
Prepare for monitoring visits and audits, assist with ISF maintenance, and address follow‑up actions. Organize exam rooms, labs, storage, and waiting areas as needed. Assist with scheduling, participant check‑in/out, and front desk coverage as applicable. Participate in community outreach events to support recruitment and engagement.
You Might Be a Great Fit If You
Have a degree in a health, science, or research‑related field or equivalent hands‑on experience in a healthcare or clinical setting. Are comfortable with clinical tools like blood pressure monitors, ECG machines, or point‑of‑care testing devices (or are eager to learn). Have strong attention to detail and can maintain accurate, compliant documentation.Enjoy working in a fast‑paced environment with changing priorities. Communicate clearly and professionally with participants, colleagues, and external partners. Are tech‑savvy and comfortable navigating Microsoft Office and clinical data systems. Thrive in a team environment but can also work independently.Bring a proactive, problem‑solving mindset to every challenge. Benefits
Comprehensive health, dental, and vision insurance Enhanced EAP– mental health support Adaptable PTO + paid holidays Continuing education reimbursement 401(k) / RRSP with company match and immediate vesting 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.
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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’re looking for a Research Assistant / Lab Specialist to support the successful execution of clinical research studies from start to finish. In this role, you’ll work closely with Investigators, Clinical Research Coordinators (CRCs), and the wider site team to ensure studies run smoothly, safely, and in full compliance with protocol and regulations. This hands‑on role is varied—some days you’ll recruit and screen participants, other days you’ll collect data, process samples, or keep study documentation organized and accurate.In addition to Research Assistant responsibilities, you will also perform routine laboratory sample collection, processing, and shipping in accordance with study protocols, laboratory manuals, SOPs, and company guidelines. Your work will directly contribute to advancing clinical research that makes a difference in patients’ lives.What You’ll Do
Support Study Protocol&Safety
Conduct study activities in compliance with GCP, SOPs, and study protocols. Monitor participant safety and well‑being throughout their study journey. Schedule and conduct study visits, including vitals, ECGs, and other protocol‑required assessments.
Sample Collection&Laboratory Procedures
Perform phlebotomy, sample collection, processing, and shipping as required by protocol. Complete requisition, labeling, storage, and shipment of specimens accurately. Conduct blood glucose testing for diabetes participants and other point‑of‑care testing (e.g., nasal swabs) as required. Perform ECGs, vital signs, meal distribution, and other clinical procedures as required by protocol/site.Perform PBMC collection, receipt of samples, isolation, and cryopreservation as required. Maintain PBMC supplies, documentation, and samples.
Recruitment, Screening&Enrollment
Assist with recruitment strategies and outreach efforts to identify eligible participants. Screen participants according to inclusion/exclusion criteria. Obtain informed consent and maintain accurate documentation.
Study Visit Execution
Perform delegated clinical tasks such as phlebotomy, sample collection and shipping, point‑of‑care testing, and investigational product accountability. Accurately complete source documents, CRFs, queries, and maintain CTMS records.
Data Integrity&Compliance
Collect and report adverse events promptly, including SAEs within required timelines. Maintain investigational product inventory, logs, and storage conditions. Conduct quality control checks to ensure data accuracy and protocol compliance.
Site&Administrative Support
Prepare for monitoring visits and audits, assist with ISF maintenance, and address follow‑up actions. Organize exam rooms, labs, storage, and waiting areas as needed. Assist with scheduling, participant check‑in/out, and front desk coverage as applicable. Participate in community outreach events to support recruitment and engagement.
You Might Be a Great Fit If You
Have a degree in a health, science, or research‑related field or equivalent hands‑on experience in a healthcare or clinical setting. Are comfortable with clinical tools like blood pressure monitors, ECG machines, or point‑of‑care testing devices (or are eager to learn). Have strong attention to detail and can maintain accurate, compliant documentation.Enjoy working in a fast‑paced environment with changing priorities. Communicate clearly and professionally with participants, colleagues, and external partners. Are tech‑savvy and comfortable navigating Microsoft Office and clinical data systems. Thrive in a team environment but can also work independently.Bring a proactive, problem‑solving mindset to every challenge. Benefits
Comprehensive health, dental, and vision insurance Enhanced EAP– mental health support Adaptable PTO + paid holidays Continuing education reimbursement 401(k) / RRSP with company match and immediate vesting 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.
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Informations clefs
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Nom de l’entrepriseCentricity Research
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Titre de posteResearch Assistant / Laboratory Specialist (Vaughan)
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