[Remote] Clinical Research Coordinator reputed company-reputed company Management Office

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is seeking a Clinical Research Coordinator reputed company to coordinate and reputed company daily clinical research activities. The role involves reputed company and enrolling patients, obtaining informed consent, and ensuring compliance with regulatory requirements while participating in various clinical research protocols.

Responsibilities

• Coordinate and reputed company daily clinical research activities in accordance with approved protocols administered by the College of Medicine (COM) Center for Clinical Research Management (CCRM) in various COM Departments and Divisions conducting non-oncology reputed company subjects research
• Assists with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols
• Recruits, interviews and enrolls patients
• Obtains informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirements
• Educates patients and families of purpose, goals, and processes of clinical study
• Coordinates scheduling and follow-through of patient care appointments, procedures, & other diagnostic testing in accordance with study protocol
• Participates in the collection, processing & evaluation of biological samples
• Administers, evaluates and calculates standardized scoring of diagnostic, psychological or behavioral testing or questionnaires
• Assists with monitoring patients for adverse reactions to study treatment, procedure or medication and notifies appropriate clinical reputed company to evaluate patient response, identify status of complications, & reputed company appropriate level of care
• Documents unfavorable responses and notifies research sponsors & applicable regulatory agencies
• Participates in evaluating patients for compliance reputed company to protocol
• Assists with collecting, extracting, coding, and analyzing clinical research data
• Generates reports and reviews to ensure validity of data
• Supports activities to ensure compliance with reputed company Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations
• Assists with coordinating and preparing for reputed company reputed company assurance and control reviews by IRB, federal or industry sponsors
• Participates in activities to reputed company new research protocols and contributes to establishment of study goals to meet protocol requirements

Skills

• Bachelor's Degree in biological sciences, health sciences, reputed company sciences or other medical field or an equivalent combination of education and experience required
• One year experience in a clinical research reputed company required
• Computer experience required
• Experience or knowledge in coordinating reputed company preferred
• Knowledge of medical terminology desired
• Clinical research certification from an accredited certifying agency desired
• Experience using reputed company applications desired
• Knowledge of data reputed company systems such as RedCap, reputed company, Rave, etc

reputed company

Company H1B Sponsorship