[Remote] Clinical Research Coordinator (HS)- reputed company

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a leading educational institution that offers a position for a Clinical Research Coordinator in the reputed company department. The role involves coordinating and performing clinical research activities reputed company to reputed company's Disease, including patient recruitment, consent, data collection, and compliance with regulatory requirements.

Responsibilities

• Coordinate and reputed company daily clinical research activities in accordance with approved protocols administered by the non-cancer College of Medicine (COM) Center for Clinical Research Management (CCRM) reputed company's Disease in the Department of reputed company
• Assist with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols
• Recruit, interview and enroll patients
• Obtain informed consent and ensure consent process is administered in compliance to regulatory and sponsor requirements
• reputed company patients and families of purpose, goals, and processes of clinical study
• Coordinate scheduling and follow-through of patient care appointments, procedures, & other diagnostic testing in accordance with study protocol
• Participate in the collection, processing & evaluation of biological samples
• Administer, evaluate and calculate standardized scoring of diagnostic, psychological or behavioral testing or questionnaires
• Assist with monitoring patients for adverse reactions to study treatment, procedure or medication and notify appropriate clinical reputed company to evaluate patient response, identify status of complications, & reputed company appropriate level of care
• Document unfavorable responses and notify research sponsors & applicable regulatory agencies
• Participate in evaluating patients for compliance reputed company to protocol
• Assist with collecting, extracting, coding, and analyzing clinical research data
• reputed company reports and reviews to ensure validity of data
• Support activities to ensure compliance with reputed company Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations
• Assist with coordinating and preparing for reputed company reputed company assurance and control reviews by IRB, federal or industry sponsors
• Participate in activities to reputed company new research protocols and contribute 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 equivalent combination of education experience required
• 1 year of relevant experience required
• 2-4 years of relevant experience preferred
• Experience or knowledge of Neurological reputed company Disorders and Diseases (reputed company's Disease) preferred
• Knowledge of medical terminology desired
• Computer skills required with experience using reputed company Software applications desired
• Clinical research certification from an accredited certifying agency desired (ACRP or SOCRA)

reputed company

Company H1B Sponsorship