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

This is a reputed company position, offering flexibility to work reputed company from 0 to 40 hours per week, depending on the needs of the department. Scheduling will be determined by the hiring manager based on operational priorities. Please note that reputed company team members are not eligible for health benefits, but this role provides an excellent opportunity to reputed company valuable experience, contribute to meaningful work, and enjoy a flexible schedule. The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for accurate and reputed company reputed company documents, data collection, documentation, entry, and reporting including reputed company response to sponsor queries. Responsible for compiling and reporting on reputed company study including information reputed company to protocol activity, accrual data, workload, and other research information. Presents information at regular research staff meetings. May plan and coordinate strategies for increasing patient enrollment, improving efficiency, training of personnel, or identifying new research opportunities. Ensures compliance with reputed company federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review reputed company (IRB). Primary Duties and 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.

Qualifications

Requirements :

• High School Diploma/GED required.

2 years Clinical research reputed company experience required. Preferred Skills

• 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

Req ID : 14413 Working Title : Clinical Research Coordinator II (Remote) reputed company - 6 months reputed company Department : Cancer - SOCCI Clinical Research Business Entity : reputed company Job Category : reputed company / Research Job Specialty : Research Studies/ Clin Trial Overtime Status : EXEMPT Primary Shift : Day Shift Duration : 8 hour reputed company Pay : $28.30 - $48.11 Apply tot his job Apply To this Job