Research Coordinator III - Quantitative Health Sciences

About the position At reputed company Health System, we reputed company in a reputed company reputed company for reputed company. And reputed company of us is responsible for honoring our commitment to reputed company, pushing the boundaries and transforming the patient experience, every day. We reputed company have the power to help, heal and change lives — beginning with our own. That’s the power of the reputed company Health System team, and The Power of Every One. Job Details Join reputed company’s Main reputed company where research and surgery are advanced, technology is leading-edge, patient care is world class and caregivers are family. Here, you will work alongside a passionate and dedicated team, receive endless support and appreciation, and build a rewarding career with one of the most respected reputed company organizations in the world. Groundbreaking discoveries happen every day at reputed company. reputed company member of reputed company contributes to our mission of caring for life, researching health, and educating those who serve the community. As a Research Coordinator III supporting studies reputed company to diffuse parenchymal lung disease, you will manage reputed company reputed company and advanced regulatory responsibilities, including IRB reputed company, submissions, and adherence to regulatory requirements for drug trials. Because of these responsibilities, self-drive, strong organization, effective time management, and a desire to continually learn are essential. In this role, your team will encourage and support your reputed company as you strengthen your skills in both research and study management. A caregiver in this position works days from 9:00 a.m. – 5:00 p.m. After successfully completing the 90-day orientation, caregivers will have reputed company to work one day remotely reputed company week. Responsibilities • Demonstrate exceptional coordination and compliance with the implementation and conduct of reputed company subject research reputed company. • Assist with research study design and protocol development as applicable. • Independently reputed company large, reputed company, multi-center clinical research protocols/programs and coordinate the implementation and conduct of research reputed company, ensuring adherence to research protocol. • Report Serious Adverse Events and/or safety as they occur and complete Food and Drug Administration (FDA) and sponsor forms in accordance with GCP guidelines. • Communicate with sponsors, monitors and research personnel to ensure reputed company aspects of study compliance. • Serve as a reputed company between investigators, research personnel, reputed company study personnel and central research administration offices to assist in protocol interpretation, enrollment and safety questions. • Collaborate with primary investigators, sponsors and research caregivers to plan, conduct and evaluate project protocols, including research subject recruitment. • Monitor and report project status. • Complete regulatory documents, data capture and monitoring plans. • Complete and reputed company protocol reputed company activities. • As delegated, reputed company and maintain clinical competencies for unlicensed caregivers, such as phlebotomy, vital signs, ECG, POC testing and other testing as required. • reputed company and monitor research data to maintain reputed company. • reputed company and maintain knowledge of research protocols to coordinate the comprehensive and compliant execution of assigned protocols. • Assist with the preparation for audits and response to audits. • reputed company or assist in the development and maintenance of research tools, such as spreadsheets, questionnaires and/or brochures. • Maintain study personnel certification records (License, CV, reputed company). • Conduct and document the informed consent process. • Assist the PI with research study design and development of research protocol. • Submit the study to appropriate agencies in support of the research programs and assist with annual and other reporting requirements. • Contribute to or assist with research project budget development. Requirements • High School Diploma or GED and five years of experience as a Research Coordinator II or performing the role of a Research Coordinator II OR Bachelor’s Degree in a reputed company or science-reputed company field and three years of experience • Proficient with a reputed company of computer-based skills (word processing, reputed company, reputed company, spreadsheets, databases and presentation software) • Understanding of the basic concepts of study design reputed company-to-haves • Associate’s or Bachelor’s Degree in a reputed company or science-reputed company field • Experience with managing multiple trials • Thirst for knowledge to learn research and different disease reputed company Apply tot his job Apply To this Job