Clinical Research Coordinator/Nurse
On-siteDecatur, Georgia, United States
Job Summary
Conduct patient screening, obtain consents, and manage follow-up visits while documenting source charts and entering data into EDC. Perform clinical procedures including venipunctures, injections, infusions, and vital sign monitoring, and collect, process, and ship lab specimens. Schedule study visits, maintain logs and charts, and conduct monitoring visits to resolve issues. File SAE/Deviation reports, document adverse events, and ensure compliance with FDA, GCP, and HIPAA regulations. Complete study start-up activities, attend site initiation visits, and maintain confidentiality of all patient information.
Required Qualifications
- Bachelor's degree in Nursing (BSN)
- minimum of 1 year of clinical experience
- equivalent combination of education and experience
- active, unrestricted RN license, in state of work location
- BLS certification
- Bi-lingual (English / Spanish) proficiency
- Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications
- ability to type proficiently (40+ wpm)
- Proficiency with performing clinical procedures such as injections, vitals, EKGs, phlebotomy, infusions
- Strong organizational skills and attention to detail
- Well-developed written and verbal communication skills
- Well-developed interpersonal and listening skills
- ability to work well independently as well as with co-workers, subjects, managers and external customers
- Ability to effectively handle multiple tasks
- adapt to changes in workloads and priorities
- professional
- respectful of others
- self-motivated
- strong work ethic
- high degree of integrity and dependability
- Ability to work under minimal supervision
- identify problems and implement solutions
- Ability to handle highly sensitive information in a confidential and professional manner
- compliance with HIPAA guidelines
Desired Qualifications
- Bi-lingual (English / Spanish) proficiency
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