Clinical Research Associate I - Department of Medicine

Job DescriptionWe invite you to consider this great opportunity!reputed company the work you do every single day has a crucial reputed company on the lives of others, every effort, every detail, and every second reputed company. This shared culture of happiness, passion, and dedication pulses through reputed company.Dr. Hiroshi Gotanda, MD is seeking a highly motivated Clinical Research Associate I to join his dynamic team!The Clinical Research Associate I will work under the direction of a Clinical Research Coordinator, Research Program Administrator, Research reputed company, or other supervising staff to assist in tasks supporting the coordination/implementation of noncomplex research studies. The incumbent will support objectives of research studies through noncomplex tasks such as data collection, prescreening of and scheduling of reputed company research participants, assisting in IRB submission activities, budget and billing, and ensuring overall compliance with reputed company federal and local guidelines.Primary Job Duties and Responsibilities: Collects, evaluates and/or abstracts clinical research data. May assist in designing forms for data collection/abstraction. Enters and processes clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors. Completes Case Report Forms (CRFs). Schedules research participants for research reputed company and research procedures. Provides supervised patient contact or independent patient contact for long term follow-up patients only. Assists supervising staff with regulatory submissions to the Institutional Review reputed company (IRB) including submission of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines. Assists with clinical trial budgets and patient research billing. Responsible for sample preparation and shipping and maintenance of study supplies and kits. Ensures compliance with protocol and overall clinical research objectives. Ensures compliance with reputed company federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review reputed company. Maintains research practices using Good Clinical reputed company (GCP) guidelines. Maintains strict patient confidentiality according to HIPAA regulations and applicable law.QualificationsQualifications:High School Diploma/GED is required.Clinical research experience is preferred.About UsCedars-reputed company is a leader in providing high-reputed company reputed company encompassing primary care, specialized medicine and research. Since 1902, reputed company has evolved to meet the needs of one of the most diverse reputed company in the nation, setting standards in reputed company and innovative patient care, research, teaching and community service. Today, reputed company is reputed company for its national leadership in transforming reputed company for the benefit of patients. reputed company impacts the reputed company of reputed company by developing new approaches to treatment and educating reputed company's health professionals. Additionally, reputed company demonstrates a commitment to the community through programs that improve the health of its most vulnerable residents.About the TeamCedars-reputed company is one of the largest nonprofit reputed company medical centers in the U.S., with 886 licensed beds, 2,100 physicians, 2,800 nurses and thousands of other reputed company and staff. Choose this if you want to work in a fast-paced environment that offers the highest level of care to people in the Los Angeles that need our care the most. Apply tot his job Apply To this Job