Qureos Mentor

Centricity Research

Centricity Research is an integrated research organization (IRO) with over 40 clinical research offices across North America. The company specializes in conducting Phase I-IV clinical research across more than 35 therapeutic areas, including pharmaceutical, biotechnology, and medical device trials. With a commitment to innovation and quality, Centricity Research has been recognized for its outstanding clinical trial experiences and diversity in clinical research, earning accolades such as 'Best Places to Work.'

<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.
</div>

Research Assistant

<div>
 
 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 Screening Coordinator to lead research-related recruitment initiatives and ensure the enrollment of high-quality patients in accordance with Centricity Research recruitment guidelines. In this role, you&rsquo;ll screen patients for participation in clinical research studies with a solid understanding of study protocols, including inclusion/exclusion criteria, relevant medications, and medical conditions.
 
 
 
 What You&rsquo;ll Do
 
 
 
 <ul>
 <li>
 Work on enrollment and retention initiatives with the Site Manager
 </li>
 <li>
 Problem solve and create contingency plans to optimize enrollment via recruitment initiatives
 </li>
 <li>
 Obtain and maintain computerized database of all ad callers
 </li>
 <li>
 Return all phone calls/email responses to interested patients within 24 - 48 hours
 </li>
 <li>
 Accurately complete recruitment tracking log and all applicable clinical trial management systems
 </li>
 <li>
 Identify appropriate study candidacy based on knowledge of sites&rsquo; recruiting and upcoming studies
 </li>
 <li>
 Complete database query reviews for study candidacy and conduct outbound calls for study interest
 </li>
 <li>
 Provide study metrics on a regular basis and provide ongoing feedback regarding outcome of recruitment initiatives
 </li>
 <li>
 Occasionally attend community lectures, health fairs or events to promote Centricity Research
 </li>
 <li>
 Promote clinical trials in the community through outreach events
 </li>
 <li>
 Complete Informed Consent and screening visits per study protocol and Centricity Research SOP
 </li>
 <li>
 Perform delegated tasks completely and accurately, including review of demographic information, medication history, medical history, obtaining vital signs (blood pressure, heart rate, temperature, and waist, weight, and height measurements
 </li>
 <li>
 Complete the source documents, case report forms, and data queries in a timely manner, accurately, and completely.
 </li>
 <li>
 Assist the Central Recruitment, Research Operations and/or Investigators with any other tasks as required
 </li>
 <li>
 Able to work in a regional setting to support sites with recruitment and screening as needed
 
 
 </li>
 </ul>
 
 You Might Be a Great Fit If You
 
 
 
 <ul>
 <li>
 Communicate clearly and comfortably with patients by phone, email, and in person
 </li>
 <li>
 Stay organized and pay attention to details, especially when managing multiple tasks like outreach, documentation, and scheduling
 </li>
 <li>
 Are curious about clinical research and excited to learn protocols, medical terminology, and research ethics
 </li>
 <li>
 Feel confident using everyday computer tools like spreadsheets, databases, and email, and are open to learning systems like CTMS or EMR
 </li>
 <li>
 Bring experience from a healthcare, research, or customer-facing role, or are ready to dive in and learn on the job
 
 
 </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 Screening Coordinator

<div>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 Screening Coordinator to lead research-related recruitment initiatives and ensure the enrollment of high-quality patients in accordance with Centricity Research recruitment guidelines. In this role, you&rsquo;ll also screen patients for participation in clinical research studies with a solid understanding of study protocols, including inclusion/exclusion criteria, relevant medications, and medical conditions. 
What You&rsquo;ll Do<ul><li>
Work on enrollment and retention initiatives with the Site Manager</li><li>
Problem solve and create contingency plans to optimize enrollment via recruitment initiatives</li><li>
Obtain and maintain computerized database of all ad callers</li><li>
Return all phone calls/email responses to interested patients within 24 - 48 hours</li><li>
Accurately complete recruitment tracking log and all applicable clinical trial management systems</li><li>
Identify appropriate study candidacy based on knowledge of sites&rsquo; recruiting and upcoming studies</li><li>
Complete database query reviews for study candidacy and conduct outbound calls for study interest</li><li>
Provide study metrics on a regular basis and provide ongoing feedback regarding outcome of recruitment initiatives</li><li>
Occasionally attend community lectures, health fairs or events to promote Centricity Research</li><li>
Promote clinical trials in the community through outreach events</li><li>
Complete Informed Consent and screening visits per study protocol and Centricity Research SOP</li><li>
Perform delegated tasks completely and accurately, including review of demographic information, medication history, medical history, obtaining vital signs (blood pressure, heart rate, temperature, and waist, weight, and height measurements</li><li>
Complete the source documents, case report forms, and data queries in a timely manner, accurately, and completely.</li><li>
Assist the Central Recruitment, Research Operations and/or Investigators with any other tasks as required</li><li>
Able to work in a regional setting to support sites with recruitment and screening as needed</li></ul> 
You Might Be a Great Fit If You:<ul><li>
Communicate clearly and comfortably with patients by phone, email, and in person</li><li>
Stay organized and pay attention to details, especially when managing multiple tasks like outreach, documentation, and scheduling</li><li>
Are curious about clinical research and excited to learn protocols, medical terminology, and research ethics</li><li>
Feel confident using everyday computer tools like spreadsheets, databases, and email, and are open to learning systems like CTMS or EMR</li><li>
Bring experience from a healthcare, research, or customer-facing role, or are ready to dive in and learn on the job</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>

Join Centricity Research and explore 3   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 Screening Coordinator

Clinical Screening Coordinator