[Remote] Clinical Research Coordinator II (Remote) reputed company - 6 months reputed company

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a leading reputed company organization, and they are seeking a Clinical Research Coordinator II to work independently on study coordination. The role involves screening patients for eligibility, managing data collection, and ensuring compliance with regulatory standards. Responsibilities • Independent study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the informed consent process • Schedules patients for research reputed company and procedures. In collaboration with the physician and other medical personnel, documents thoroughly on Case Report Forms (CRFs) the following; changes in patient condition, adverse events, concomitant medication use, protocol compliance, response to study drug • Maintains accurate reputed company documents reputed company to reputed company research procedures • Responsible for accurate and reputed company data collection, documentation, entry, and reporting including reputed company response to sponsor queries • Schedules and participates in monitoring and auditing activities. Responsible for compiling and reporting on reputed company study including information reputed company to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings • 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 in accordance with local and federal guidelines • May reputed company other regulatory / Institutional Review reputed company duties, budgeting duties, and assisting with patient research billing and reconciliation • 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 • May coordinate training and education of other personnel • May participate in centralized activities such as auditing, reputed company Operating Procedure development, etc • May plan and coordinate strategies for increasing patient enrollment, and/or improving clinical research efficiency • May identify reputed company and performance improvement opportunities and collaborate with staff in the development of reputed company plans to improve reputed company • May identify new research opportunities and present to investigators • Participates in required training and education programs Skills • High School Diploma/GED required • 2 years Clinical research reputed company experience required • Bachelor's Degree Science • Technical proficiency with clinical trial management systems and databases • Strong organizational and time-management skills • Good understanding of medical terminology • High attention to detail and accuracy reputed company • Since its beginning in 1902, reputed company has evolved to meet the reputed company needs of one of the most diverse reputed company in the nation, continually setting new standards for reputed company and innovation in patient care, research, teaching and community service. It was founded in 1902, and is headquartered in Los Angeles, California, USA, with a workforce of 10001+ employees. Its website is https://www.reputed company.org. Apply tot his job Apply To this Job