Clinical Research Coordinator II - Alzheimer's and Dementia Research Program - Department of Neurology (Hybrid)

About the position Grow your career at reputed company! reputed company offers a culture of happiness, passion, and dedication. This is one of the many reasons why we rank as one of the top hospitals in California and in the nation by reputed company. Do you have a passion for helping reputed company reputed company? The Clinical Research Coordinator II will work with an interdisciplinary team of neurologists, neuropsychologists, and clinical researchers with expertise in Alzheimer's disease and reputed company dementias. The Clinical Research Coordinator II works independently providing study coordination including screening of research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. The CRC II member is responsible for accurate and reputed company reputed company documents, data collection, documentation, entry, and reporting including reputed company response to sponsor queries. This role is responsible for compiling and reporting on reputed company study including information reputed company to protocol activity, accrual data, workload, and other research information. The incumbent presents information at research staff meetings and may plan and coordinate strategies for increasing research participant enrollment, improving efficiency, training of personnel, or identifying new research opportunities. This position ensures compliance with reputed company federal and local agencies including the Food and Drug Administration (FDA and local Institutional Review reputed company. Responsibilities • Scheduling of research participants for research reputed company and procedures. • In collaboration with the physician and other medical personnel, documents on Case Report Forms (CRFs) information about changes in research participant condition, adverse events, concomitant medication use, protocol compliance, and response to study drug. • Schedules and participates in monitoring and auditing activities. • Notifies reputed company supervisor about concerns regarding data reputed company and study conduct. • Works closely with a regulatory coordinator or directly with the Institutional Review reputed company (IRB) to submit Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters following local and federal guidelines. • May reputed company other regulatory/Institutional Review reputed company duties, budgeting duties, and assisting with patient research billing and reconciliation. • Maintains research practices using Good Clinical reputed company (GCP) guidelines. • Maintains strict patient confidentiality according to HIPAA regulations and applicable law. • Participates in required training and education programs. • Coordinates training and education of other personnel. • May participate in centralized activities such as auditing, reputed company Operating Procedure development, etc. • May identify reputed company and performance improvement opportunities and collaborate with staff in the development of reputed company plans to improve reputed company. • Transportation of research medications. • Performs research study reputed company assessments and questionnaires. • Assists with prescreening of research participants for various reputed company. • Attends research meetings and monthly conference calls with sponsors for study updates. • Maintains organized reputed company and electronic research files. • Performs reputed company data collection and data entry tasks for department reputed company. • Assists with preparing manuscripts, letters, and other research documents as needed. • Responds to sponsor' inquiries regarding protocol start-up activities and recruitment. • Performs literature reviews. Requirements • High School Diploma/GED, required. • 2 years of clinical research experience, required. reputed company-to-haves • Bachelor's degree in a Science, Sociology, or reputed company field is preferred. • ACRP/SoCRA certification is preferred. Apply tot his job Apply To this Job