Clinical Research Coordinator I

OverviewClinical 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 RoleWe’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.What You’ll DoStudy Coordination & Participant SafetyEnsure the safety and well-being of all study participantsConduct study visits in line with protocol, GCP, and internal SOPsCollect study-specific assessments (e.g., vitals, ECGs) and maintain documentation accuracyObtain and maintain proper informed consentRecruitment, Screening & EnrollmentPromote and support recruitment initiatives to identify eligible study participantsScreen participants according to protocol inclusion/exclusion criteriaGuide participants through the consent process and ensure proper documentationSchedule and coordinate study visits across the full lifecycle of participationStudy Execution & Data CollectionPerform clinical tasks such as phlebotomy, sample processing/shipping, point-of-care testing, and participant monitoringAccurately complete source documentation, CRFs, queries, and maintain CTMS recordsDispense and track investigational products according to protocolCollect and report adverse events, including timely SAE reportingParticipate in site feasibility questionnaires (FQs) and pre-study visits (PSVs) to support site readiness and study start-up activitiesQuality, Compliance & Site SupportPrepare for monitoring visits, audits, and maintain regulatory filesPerform regular quality control checks on source data and documentsSupport lab supply inventory, equipment maintenance, and administrative needsAssist with community engagement and outreach events as neededYou Might Be a Great Fit If YouHave a bachelor’s degree in a health, science, or research-related field (or equivalent combination of education and experience)Have 2–4 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)Have phlebotomy experience — or are open to learning it where permitted by law (we’ll provide the training). Understand basic medical terminology, or are eager to learn it quicklyAre passionate about contributing to clinical trials that impact global healthAre organized, detail-oriented, and skilled at multitasking in a fast-paced environmentAre proactive, collaborative, and take ownership of your workValue open communication and thrive in a team-driven environmentWhy Centricity Research?Our MissionWe connect people to scientific advancements through groundbreaking research within a deeply human experience.Our Core ValuesQuality: 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.BenefitsComprehensive health, dental, and vision insuranceEnhanced EAP – mental health supportFlexible PTO + paid holidaysContinuing education reimbursement401(k) / RRSP with company match and immediate vestingReady to Apply?We’d love to hear from you – apply nowWe’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. #J-18808-Ljbffr