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Clinical Research Coordinator at Arkansas Urology
Little Rock, Arkansas, United States -
Full Time

Start Date

Immediate

Expiry Date

08 May, 26

Salary

0.0

Posted On

07 Feb, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Data Abstraction, Patient Recruitment, Informed Consent, Database Management, Regulatory Compliance, Data Management, Specimen Collection, Problem Identification, Study Promotion, Audit Participation, Attention to Detail, Analytical Mindset, Patient Education, Research Protocols, Medical Experience, Enthusiasm for Learning

Industry

Hospitals and Health Care

Description
Description Clinical Research Coordinator Little Rock, AR Description GENERAL DESCRIPTION OF POSITION The Clinical Research Coordinator ensures that all study activity is in accordance with guidelines, instructions and specifications outlined in the research protocol. ESSENTIAL DUTIES AND RESPONSIBILITIES 1. Reviews and abstracts data from medical record charts to screen patients based on inclusion/exclusion criteria. 2. Recruits, screens, and obtains consent from program participants. 3. Enters patient information into clinical research database and maintains patient information in research database to ensure proper research accounting. 4. Assures compliance with all relevant IRB and other regulatory agency requirements. 5. Collects, manages, and maintains patient and laboratory data for clinical research studies. 6. Coordinates collection and shipment of required specimens for protocol if applicable. 7. Identifies problems or obstacles in the system/procedures related to implementation of the research protocols. 8. Promotes use of open and available clinical studies to appropriate health care providers and venues. 9. Participates in audits of assigned protocols. 10. Perform any other related duties as required or assigned. Requirements EDUCATION AND EXPERIENCE Equivalent to an Associate degree in nursing or other medical related area, plus two (2) years related medical experience and/or training, or equivalent combination of education and experience. Analytical mindset and attention to detail. Enthusiasm for learning is required as is participation in educating patients and other personnel to the research process.
Responsibilities
The Clinical Research Coordinator ensures compliance with research protocols and manages study activities. Responsibilities include recruiting participants, maintaining databases, and coordinating specimen collection.