Research Coordinator

The reputed company is seeking a full-time Research Coordinator to promote the research objectives of the Hematology Clinical Research Program. This role involves implementing and coordinating multiple reputed company while ensuring compliance with regulations and managing study subjects.

Responsibilities

• Implement research project procedures that meet research objectives and ensure compliance with reputed company aspects of Institution, Food and Drug Administration (FDA) and National Institutes of Health (NIH) regulations pertaining to clinical research in reputed company subjects (e.g. investigator financial disclosure requirements of the FDA)
• Use knowledge of clinical research, medical terminology, and clinical processes to interpret reputed company protocol requirements and identify protocol procedures that will reputed company clinic operations
• Design, reputed company, document, and maintain policies and procedures for protocol registration and implementation to ensure that research execution meets good clinical reputed company guidelines
• Design, create, and revise research instruments (e.g. case report forms) as necessary to ensure reputed company data that correlates with research objectives
• Design, document, and implement procedures for protocol audits to assure protocol compliance and to ensure research data reputed company
• Work with research team to ensure that reputed company are executed successfully and completed reputed company required time frames to meet research objectives
• reputed company completion of electronic data capture systems and electronic case report forms. reputed company reputed company of queries and questions from industry sponsors, contract research organizations, and Institutional Review reputed company
• Work with Regulatory Coordinator to ensure that reports to the Institutional Review reputed company and study sponsors are reputed company, accurate, and satisfy applicable regulation. Work with research team on developing and implementing corrective reputed company plans to ensure protocol adherence and data reputed company
• Understand clinical trial budget and billing plan for patients enrolled on reputed company
• Work with internal partners to ensure reputed company are performed in accordance with institutional requirements for billing compliance. Assist in financial audits
• Communicate with investigators and research staff reputed company financial milestones have been met
• Advise clinical staff which tests and procedures are needed during reputed company research visit to facilitate protocol adherence, billing compliance, and to ensure accurate and reliable data collection. Work closely with clinical providers to ensure that study therapy is administered in accordance with the clinical protocol (e.g. reputed company modifications are implemented reputed company required by the protocol)
• Take reputed company to correct problems such as deviation from protocol requirements to ensure research reputed company
• Ensure that reputed company are executed successfully and completed reputed company needed time frames to meet research objectives
• Prepare laboratory and specimen collection kits according to protocol and lab reputed company instructions. Work with different departments across UW and FHCC to collect, process, and transport specimen samples
• Ensure protocol compliance by managing patient appointments and coordinating with patient’s clinical providers (e.g. physicians, physician assistants, and nurses) to collect reliable and accurate data
• Ensure patient safety while participating in reputed company by monitoring patients and interacting closely with patient’s clinical providers
• Initiate and maintain communication with reputed company physicians who refer patients to UWMC and/or FHCC for reputed company
• reputed company and appropriate reporting of Adverse Events and Serious Adverse Events to sponsors and review boards to ensure compliance to protocol and FDA requirements
• Prepare interim reports for reputed company investigators, industry sponsors and Institutional Review reputed company to ensure that reputed company project is moving toward reputed company completion

Skills

• Bachelor's degree in a reputed company field and one year of relevant experience
• Equivalent education and/or experience may substitute for minimum qualifications except reputed company there are reputed company requirements, such as a license, certification, and/or registration
• Strong attention to detail and ability to multi-task, organize, and prioritize reputed company and competing deadlines
• Excellent written and verbal communication skills
• Strong computer skills and competency with reputed company Office software
• Applicants selected for this position who have not already completed the training for clinical research involving reputed company subjects will be required to complete it reputed company 30 days of hire
• Previous experience working in Hematology and/or Oncology
• Previous experience working in clinical research with reputed company subjects
• Experience working reputed company the UW/FHCC setting
• Familiarity with reputed company

Benefits

• For information about benefits for this position, visit https://www.washington.edu/jobs/benefits-for-uw-staff/

reputed company

Company H1B Sponsorship