Join to apply for the Clinical Research Associate role at University of Southern California . The USC Keck School of Medicine - Alzheimer Therapeutic Research Institute (ATRI), located in San Diego, California, is an academic institute comprised of an expert panel of scientific collaborators committed to advancing the development of new treatments for Alzheimer’s Disease (AD) through innovative clinical trials. Duties The incumbent will provide oversight of the progress of clinical trials at study sites, ensuring they are conducted, recorded, and reported in accordance with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and applicable regulatory requirements. Responsibilities include but are not limited to: Conduct onsite and remote monitoring for assigned clinical sites, review Investigator Site Files, study data, perform IP reconciliation, review Informed Consent Forms, and other monitoring activities. Ensure sites follow GCP, regulatory requirements, study protocol, and ATRI policies. Document deviations from standard procedures. Review study data, manage queries, review inclusion and exclusion criteria, and ensure participant safety and protocol compliance. Serve as the main contact for assigned clinical sites. Develop a thorough understanding of the study protocol and manuals. Collaborate with Lead Clinical Monitors/Leads to escalate site compliance issues. Participate in monitoring activities to meet study milestones. Utilize internal and study-specific software and tools. Assist in training new monitors on study-specific or onsite procedures. Participate in sponsor, internal, and regulatory audits. Assist with eTMF filing efforts. Experience in AD research is preferred. Up to 50% travel may be required. Location: San Diego, CA The hourly rate range for this position is $42.02 - $57.51. USC considers various factors when extending employment offers, including experience, education, skills, and organizational needs. USC is committed to fair employment practices, including consideration of applicants with criminal records, in compliance with applicable laws. Minimum Education and Experience Bachelor's degree or equivalent experience/education Minimum of 2 years monitoring clinical trials and understanding of medical terminology Knowledge Requirements Thorough knowledge of ICH guidelines, GCP, FDA regulations, and local/country-specific regulations pertaining to clinical trials. Additional Details Seniority level: Entry level Employment type: Full-time Job function: Research, Analyst, and Information Technology Industry: Higher Education #J-18808-Ljbffr University of Southern California
...products used by hunters, property owners, and others for real-time remote monitoring. We take pride in developing deep user... ...a Team.; Grow or Die. Job Summary The Operations Project Manager will work with the Product and Software PMs to ensure that the...
...We are actively seeking qualified candidates for the following position for our client, who is an industry leader:Job Title: Data GovernanceLocation: Bridgewater, NJ/ New York NY (Hybrid - 3 days Onsite per week)Job Type: Full-TimeJob Summary: The Data Steward/...
...Job Description Job Description Salary: Human Resources Internship Spring 2025 About the Role: In this exciting internship,... ...you'll gain valuable hands-on experience in the dynamic field of HR. You'll work alongside our human resources team to support various...
...As a Neurologist, successful candidates would be expected to participate in the clinical, educational, and research activities at Hebrew SeniorLife, Deanna and Sidney Wolk Center for Memory Health. Clinical cognitive care is provided in the Deanna and Sidney Wolk Center...
...Summary This role focuses on providing medical and clinical support services to... ...vitals and documents patient information; assists physicians with procedures and educates... ...care and/or scientific/laboratory jobs. An entry-level role typically requiring little to no prior...