LPN - 251900

**Seeking a Clinical Research Nurse in Media, PA***Clinical Research NurseLocation: Media & Infrequent travel to West Chester, PA (Onsite) Department: Clinical OperationsReports To: Head of Site OperationsLeading private equity-backed clinical research site network focused on advancing innovative treatments and improving patient access to cutting-edge therapies. Our mission is to connect patients and their families with groundbreaking clinical trials through a high-quality, therapeutically focused network.Position OverviewThe Clinical Research Nurse works closely with the Principal Investigator to support and manage clinical trials from study start-up through closeout. This role is responsible for ensuring the quality, integrity, and compliance of assigned studies in accordance with Good Clinical Practice (GCP) and applicable regulations, while delivering exceptional patient care.Key ResponsibilitiesStudy Execution & OversightManage all aspects of assigned clinical trials from initiation through closeoutEnsure compliance with study protocols, GCP, and regulatory requirementsCoordinate and perform study visits and procedures per protocolAssist with monitoring visits, investigator meetings, and query resolutionPatient Care & EngagementProvide high-quality care and an excellent experience for study participantsEducate patients and support the informed consent processServe as a clinical resource for patients and internal teamsInvestigational Product (IP) ManagementPrepare, administer, and track study medications per protocol and pharmacy manualEnsure proper handling, documentation, and return of investigational productsPerform IV infusions and IM injections (intraarticular experience a plus)Lab & Sample ManagementCoordinate with lab teams to manage sample collection, processing, and shipmentReview and adhere to laboratory manuals and study-specific requirementsSafety & ComplianceReport all Serious Adverse Events (SAEs) to the Principal Investigator, Sponsor, and IRB within required timelines (24 hours)Maintain accurate study documentation, visit logs, and CTMS updatesSupport quality assurance activities, including audits, risk assessments, and corrective action plansQualificationsStrong communication and interpersonal skillsHigh level of organization and attention to detailAbility to multitask and work in a fast-paced environmentStrong critical thinking and problem-solving skillsAbility to prioritize and manage deadlines effectivelyEducation & ExperienceBSN, RN, or LPN requiredExperience with IV infusions and IM injections required2+ years of clinical research experience preferredCCRC certification preferred