Clinical Screening Coordinator (Regional West) at Centricity Research

Toronto, Ontario, Canada -

Full Time

Start Date

Immediate

Expiry Date

20 Jul, 26

Salary

50000.0

Posted On

21 Apr, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical research, Patient recruitment, Study protocols, Inclusion/exclusion criteria, Data management, Patient screening, Medical terminology, Research ethics, Database management, Communication, Documentation, Vital signs measurement, Case report forms, Outreach, Problem solving, Time management

Industry

Biotechnology Research

Description

About the Role We’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’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. This is a regional role that will be based out of one of our Etobicoke locations in Toronto with required travel to our other Etobicoke and Brampton locations as needed. What You’ll Do Work on enrollment and retention initiatives with the Site Manager Problem solve and create contingency plans to optimize enrollment via recruitment initiatives Obtain and maintain computerized database of all ad callers Return all phone calls/email responses to interested patients within 24 - 48 hours Accurately complete recruitment tracking log and all applicable clinical trial management systems Identify appropriate study candidacy based on knowledge of sites’ recruiting and upcoming studies Complete database query reviews for study candidacy and conduct outbound calls for study interest Provide study metrics on a regular basis and provide ongoing feedback regarding outcome of recruitment initiatives Occasionally attend community lectures, health fairs or events to promote Centricity Research Promote clinical trials in the community through outreach events Complete Informed Consent and screening visits per study protocol and Centricity Research SOP 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 Complete the source documents, case report forms, and data queries in a timely manner, accurately, and completely. Assist the Central Recruitment, Research Operations and/or Investigators with any other tasks as required Able to work in a regional setting to support sites with recruitment and screening as needed You Might Be a Great Fit If You: Bachelor's degree in a health, science, or research-related field, or equivalent combination of education and experience Communicate clearly and comfortably with patients by phone, email, and in person Stay organized and pay attention to details, especially when managing multiple tasks like outreach, documentation, and scheduling Are curious about clinical research and excited to learn protocols, medical terminology, and research ethics Feel confident using everyday computer tools like spreadsheets, databases, and email, and are open to learning systems like CTMS or EMR Bring experience from a healthcare, research, or customer-facing role, or are ready to dive in and learn on the job 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.

Responsibilities

The Clinical Screening Coordinator leads research-related recruitment initiatives and screens patients for clinical study participation based on protocol criteria. They are responsible for maintaining recruitment logs, managing databases, and performing clinical tasks such as obtaining vital signs and completing source documents.