Qureos Mentor

Centricity Research

<div>Research Assistant (RA)
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&rsquo;re looking for a Research Assistant (RA) to support the successful execution of clinical research studies from start to finish. In this role, you&rsquo;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&mdash;some days you&rsquo;ll recruit and screen participants, other days you&rsquo;ll collect data, process samples, or keep study documentation organized and accurate. Your work will directly contribute to advancing clinical research that makes a difference in patients&rsquo; lives. 
What You&rsquo;ll Do 
Support Study Protocol &amp; Safety<ul><li>
Conduct study activities in compliance with GCP, SOPs, and study protocols.</li><li>
Monitor participant safety and well-being throughout their study journey.</li><li>
Schedule and conduct study visits, including vitals, ECGs, and other protocol-required assessments.</li></ul>
Recruitment, Screening &amp; Enrollment<ul><li>
Assist with recruitment strategies and outreach efforts to identify eligible participants.</li><li>
Screen participants according to inclusion/exclusion criteria.</li><li>
Obtain informed consent and maintain accurate documentation.</li></ul>
Study Visit Execution<ul><li>
Perform delegated clinical tasks such as phlebotomy, sample collection and shipping, point-of-care testing, and investigational product accountability.</li><li>
Accurately complete source documents, CRFs, queries, and maintain CTMS records.</li></ul>
Data Integrity &amp; Compliance<ul><li>
Collect and report adverse events promptly, including SAEs within required timelines.</li><li>
Maintain investigational product inventory, logs, and storage conditions.</li><li>
Conduct quality control checks to ensure data accuracy and protocol compliance.</li></ul>
Site &amp; Administrative Support<ul><li>
Prepare for monitoring visits and audits, assist with ISF maintenance, and address follow-up actions.</li><li>
Organize exam rooms, labs, storage, and waiting areas as needed.</li><li>
Assist with scheduling, participant check-in/out, and front desk coverage (as applicable).</li><li>
Participate in company or community outreach events to support recruitment and engagement.</li></ul>
You Might Be a Great Fit If You:<ul><li>
Have a degree in a health, science, or research-related field or equivalent hands-on experience in a healthcare or clinical setting.</li><li>
Are comfortable with clinical tools like blood pressure monitors, ECG machines, or point-of-care testing devices (or are eager to learn).</li><li>
Have strong attention to detail and can maintain accurate, compliant documentation.</li><li>
Enjoy working in a fast-paced environment with changing priorities.</li><li>
Communicate clearly and professionally with participants, colleagues, and external partners.</li><li>
Are tech-savvy and comfortable navigating Microsoft Office and clinical data systems.</li><li>
Thrive in a team environment but can also work independently.</li><li>
Bring a proactive, problem-solving mindset to every challenge.</li></ul>
Why Centricity Research?
Our Mission
We connect people to scientific advancements through groundbreaking research within a deeply human experience. 
Our Core Values<ul><li> 
Quality: We aim for excellence and integrity in everything we do - because lives depend on it.</li><li>
Care: We show up for each other, our customers, and our mission - always going the extra mile.</li><li>
Be the Change You Seek: We're adaptable, forward-thinking, and constantly improving - for the betterment of all.</li><li>
One Team: We collaborate, support one another, and succeed together.</li><li>
Grow for Good: We grow with purpose - to expand access to research and improve global health.</li><li>
Own It: We take initiative, deliver results, and follow through - with passion and accountability.</li></ul>
Benefits<ul><li>
Comprehensive health, dental, and vision insurance</li><li>
Enhanced EAP &ndash; mental health support</li><li>
Flexible PTO + paid holidays</li><li>
Continuing education reimbursement</li><li>
401(k) / RRSP with company match and immediate vesting</li></ul>
Ready to Apply?
We&rsquo;d love to hear from you &ndash; apply now! 
We&rsquo;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.<ul><li> 
This is a fully on-site role. The starting salary range for this role is $40,000 - $45,000.</li></ul></div>

Research Assistant

<div>Clinical Research Coordinator I (CRC I)
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&rsquo;re looking for a Clinical Research Coordinator I (CRC I) to support the successful execution of clinical studies by managing a mix of administrative and clinical tasks. In this role, you&rsquo;ll work closely with Investigators to ensure study activities are organized, compliant, and aligned with protocol requirements. The CRC I brings strong attention to detail and a solid grasp of study protocols, helping keep research operations running smoothly, accurately, and on time. 
What You&rsquo;ll Do
Study Coordination &amp; Participant Safety<ul><li>
Ensure the safety and well-being of all study participants</li><li>
Conduct study visits in line with protocol, GCP, and internal SOPs</li><li>
Collect study-specific assessments (e.g., vitals, ECGs) and maintain documentation accuracy</li><li>
Obtain and maintain proper informed consent</li></ul>
Recruitment, Screening &amp; Enrollment<ul><li>
Promote and support recruitment initiatives to identify eligible study participants</li><li>
Screen participants according to protocol inclusion/exclusion criteria</li><li>
Guide participants through the consent process and ensure proper documentation</li><li>
Schedule and coordinate study visits across the full lifecycle of participation</li></ul>
Study Execution &amp; Data Collection<ul><li>
Perform clinical tasks such as phlebotomy, sample processing/shipping, point-of-care testing, and participant monitoring</li><li>
Accurately complete source documentation, CRFs, queries, and maintain CTMS records</li><li>
Dispense and track investigational products according to protocol</li><li>
Collect and report adverse events, including timely SAE reporting</li><li>
Participate in site feasibility questionnaires (FQs) and pre-study visits (PSVs) to support site readiness and study start-up activities</li></ul>
Quality, Compliance &amp; Site Support<ul><li>
Prepare for monitoring visits, audits, and maintain regulatory files</li><li>
Perform regular quality control checks on source data and documents</li><li>
Support lab supply inventory, equipment maintenance, and administrative needs</li><li>
Assist with community engagement and outreach events as needed</li></ul>
You Might Be a Great Fit If You:<ul><li>
Have a bachelor&rsquo;s degree in a health, science, or research-related field (or equivalent combination of education and experience)</li><li>
Have 2&ndash;4 years of experience in a healthcare setting and are comfortable with clinical tools like blood pressure monitors, ECG machines, and weight scales (nice to have, but not required)</li><li>
Have phlebotomy experience &mdash; or are open to learning it where permitted by law (we&rsquo;ll provide the training).Understand basic medical terminology, or are eager to learn it quickly</li><li>
Are passionate about contributing to clinical trials that impact global health</li><li>
Are organized, detail-oriented, and skilled at multitasking in a fast-paced environment</li><li>
Are proactive, collaborative, and take ownership of your work</li><li>
Value open communication and thrive in a team-driven environment</li></ul>
Why Centricity Research?
Our Mission
We connect people to scientific advancements through groundbreaking research within a deeply human experience. 
Our Core Values<ul><li>
Quality: We aim for excellence and integrity in everything we do - because lives depend on it.</li><li>
Care: We show up for each other, our customers, and our mission - always going the extra mile.</li><li>
Be the Change You Seek: We're adaptable, forward-thinking, and constantly improving - for the betterment of all.</li><li>
One Team: We collaborate, support one another, and succeed together.</li><li>
Grow for Good: We grow with purpose - to expand access to research and improve global health.</li><li>
Own It: We take initiative, deliver results, and follow through - with passion and accountability.</li></ul>
Benefits<ul><li>
Comprehensive health, dental, and vision insurance</li><li>
Enhanced EAP &ndash; mental health support</li><li>
Flexible PTO + paid holidays</li><li>
Continuing education reimbursement</li><li>
401(k) / RRSP with company match and immediate vesting</li></ul>
Ready to Apply?
We&rsquo;d love to hear from you &ndash; apply now!
We&rsquo;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.</div>

Clinical Research Coordinator I

Join Centricity Research and explore 2   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

Centricity Research

ABOUT_COMPANY

Research Assistant

Clinical Research Coordinator I