LPN

**Seeking a Clinical Research Nurse in Media, PA***If you would like to know a bit more about this opportunity, or are considering applying, then please read the following job information.Clinical Research Nurse Location:Media & Infrequent travel to West Chester, PA (Onsite) Department:Clinical Operations Reports To:Head of Site Operations Leading 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 Overview TheClinical Research Nurseworks 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 Responsibilities Study Execution & Oversight Manage all aspects of assigned clinical trials from initiation through closeout Ensure compliance with study protocols, GCP, and regulatory requirements Coordinate and perform study visits and procedures per protocol Assist with monitoring visits, investigator meetings, and query resolution Patient Care & Engagement Provide high-quality care and an excellent experience for study participants Educate patients and support the informed consent process Serve as a clinical resource for patients and internal teams Investigational Product (IP) Management Prepare, administer, and track study medications per protocol and pharmacy manual Ensure proper handling, documentation, and return of investigational products Perform IV infusions and IM injections (intraarticular experience a plus) Lab & Sample Management Coordinate with lab teams to manage sample collection, processing, and shipment Review and adhere to laboratory manuals and study-specific requirements Safety & Compliance Report all Serious Adverse Events (SAEs) to the Principal Investigator, Sponsor, xywuqvp and IRB within required timelines (24 hours) Maintain accurate study documentation, visit logs, and CTMS updates Support quality assurance activities, including audits, risk assessments, and corrective action plans Qualifications Strong communication and interpersonal skills High level of organization and attention to detail Ability to multitask and work in a fast-paced environment Strong critical thinking and problem-solving skills Ability to prioritize and manage deadlines effectively Education & Experience BSN, RN, or LPN required Experience with IV infusions and IM injections required 2+ years of clinical research experience preferred CCRC certification preferred