Clinical Research Coordinator I at Centricity Research

London, Ontario, Canada -

Full Time

Start Date

Immediate

Expiry Date

23 Jan, 26

Salary

0.0

Posted On

25 Oct, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Attention to Detail, Study Coordination, Participant Safety, Recruitment, Screening, Enrollment, Data Collection, Quality Control, Compliance, Phlebotomy, Medical Terminology, Multitasking, Communication, Teamwork, Organizational Skills

Industry

Biotechnology Research

Description

Job Details Job Location: London, ON Salary Range: Undisclosed Description Clinical Research Coordinator I (CRC I) - Temporary Full-Time 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 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’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. This is a temporary, full-time position. What You’ll Do Study Coordination & Participant Safety Ensure the safety and well-being of all study participants Conduct study visits in line with protocol, GCP, and internal SOPs Collect study-specific assessments (e.g., vitals, ECGs) and maintain documentation accuracy Obtain and maintain proper informed consent Recruitment, Screening & Enrollment Promote and support recruitment initiatives to identify eligible study participants Screen participants according to protocol inclusion/exclusion criteria Guide participants through the consent process and ensure proper documentation Schedule and coordinate study visits across the full lifecycle of participation Study Execution & Data Collection Perform clinical tasks such as phlebotomy, sample processing/shipping, point-of-care testing, and participant monitoring Accurately complete source documentation, CRFs, queries, and maintain CTMS records Dispense and track investigational products according to protocol Collect and report adverse events, including timely SAE reporting Quality, Compliance & Site Support Prepare for monitoring visits, audits, and maintain regulatory files Perform regular quality control checks on source data and documents Support lab supply inventory, equipment maintenance, and administrative needs Assist with community engagement and outreach events as needed You Might Be a Great Fit If You: Have a Science/Health educational background (minimum college diploma), or research-related field (or equivalent combination of education and experience) Have 1–2 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) Have phlebotomy experience. Understand basic medical terminology, or are eager to learn it quickly Are passionate about contributing to clinical trials that impact global health Are organized, detail-oriented, and skilled at multitasking in a fast-paced environment Are proactive, collaborative, and take ownership of your work Value open communication and thrive in a team-driven environment 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. 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. Qualifications

Responsibilities

The Clinical Research Coordinator I will support the execution of clinical studies by managing administrative and clinical tasks. This includes ensuring participant safety, conducting study visits, and maintaining compliance with study protocols.