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
Hostaway is a SaaS startup that is transforming the vacation rental industry. With innovative solutions and partnerships with giants like Airbnb, VRBO, and Booking, we're taking on the competition and winning. Leveraging our customer-centric core values, we consistently...
...information about benefits and eligibility, please visit our Benefits Page ! Minimum - Any retail experience - Any bakery/cake decorating experience - Ability to handle stressful situations - Knowledge of basic math - Effective communication skills...
We are looking for a Project Manager . This is a hybrid position based in Cracow or Warsaw, with on-site work required twice a week. What you will Do: The position includes managing, leading and controlling cross-organizational B2B projects, characterizing...
As an Esthetician at European Wax Center at HHLA, your waxing expertise will ensure every moment is an opportunity for confidence! Our ideal candidate is goal-oriented, accountable, a team player, and takes pride in their appearance. We seek a special person who has a love...
...We are seeking an experienced Medical Surgical Coder to join our clients'team. This role requires a minimum of 2 years of hands-on coding experience in a hospital or healthcare setting. While certification is preferred, it does not substitute for the required experience...