Clinical Research Coordinator (RN/LPN)

Lead Clinical Research Coordinator (RN/LPN)Role Type: Clinical Research / Site OperationsExperience Level: AssociateSetting: Research Site / Clinical TrialsRole PurposeThe Clinical Research Coordinator (act as lead) serves as the primary site-level coordinator responsible for overseeing multiple active clinical trials, with a strong focus on patient safety, protocol compliance, and operational excellence. This role leads site logistics, supports vendor and stakeholder coordination, and addresses complex protocol-related and Alzheimer’s disease–related questions.The coordinator is actively involved across the full study lifecycle, including patient recruitment, enrollment, retention, data collection, and regulatory compliance, while working closely with investigators, site staff, and cross-functional teams.Key ResponsibilitiesConduct clinical studies in compliance with FDA regulations, GCP, and ICH guidelinesEnsure patient safety and quality of care at all timesCoordinate and schedule subject visits within protocol-defined windowsPerform study procedures, including:Informed consentScreening and enrollmentVital signs, ECGs, height/weight measurementsPregnancy testing and other protocol-defined proceduresAccurately document patient data in required study systems and forms (CRFs, EDC)Maintain and update source documents and patient recordsManage investigational product (IP) accountability, when requiredEnsure IRB approvals are obtained prior to study initiation and maintained throughout the studyIdentify and report suspected protocol deviations or non-complianceParticipate in site initiation visits (SIVs) and protocol training sessionsSupport patient outreach activities, including scheduling, follow-ups, and result notificationsPromote patient engagement and retention through strong relationship-buildingAdhere to company policies, SOPs, and clinical operating proceduresAssist with facility upkeep and proper waste disposal per regulatory standardsEducation & ExperienceBachelor’s degree or equivalent in a clinical or medical-related fieldActive nursing license required (RN, LPN, or LVN), registered with the local healthcare authorityMinimum 2+ years of relevant clinical research or comparable experienceRequired Knowledge, Skills & AbilitiesStrong understanding of clinical research operations, including:GCP and SOPsInformed consent processSafety monitoring and regulatory complianceAbility to work independently with high attention to detailStrong analytical, problem-solving, and decision-making skillsDemonstrated discretion and sound judgment in handling sensitive informationEffective communication and interpersonal skillsStrong organizational and time-management abilitiesProficiency with basic computer applications and clinical systemsAbility to collaborate effectively in a team-based clinical environmentEnglish fluency preferred