Research Nurse Coordinator, RN (62974)
- Recruits and screens potential patients and obtains informed consent.
- Assists in providing patient education including benefits and risks of participating in a clinical trial
- Follows clinical trial protocols to accurately and efficiently collect and document participant data including, but not limited to, laboratory collection and processing, vital assessments, and study-specific procedures
- Provides direct nursing care according to UD's standards of practice.
- Administers investigational product (IP) per clinical trial protocol requirements.
- Completes clinical assessments and safety evaluations of study subjects and notifies study principal Investigator and Sponsor and study team per reporting guidelines.
- Maintains data management per study requirements and contractual obligations.
- Completes required study trainings and maintains strong knowledge of clinical and research protocols.
- Maintains equipment and supply resources for research studies.
- Performs upkeep of exam and work rooms with regard to sterilization, infection control, supplies, and equipment.
- Follows all CLIA Patient Safety Goals, including observing strict infectious disease precautions when handling blood specimens and IATA for specimen shipment.
- Answers emails, voicemails, and returns patient calls in a timely and efficient, and professional manner.
- Work with internal teams to ensure patients are properly compensated for visits completed per study schedule by documenting appropriate procedure completion.
- Abides by and promotes HIPAA compliance; maintains strictest confidentiality.
- Participates in staff meetings as directed by the principal investigators and Clinical Research Manager.
- Cross trains and performs other functions as directed by the principal investigators and Clinical Research Manager.
- Any other duties and/or special projects as assigned within the research department.
- Maintains strong relationships with Principal Investigator and Sub-Investigators on assigned studies
- Assists other Clinical Research Coordinators and Clinical Research Nurses on study visits as backup coordinator when required and able per delegation of authority logs.
- Performs any other duties and/or special projects as assigned
- Required:
- Licensure as a Registered Nurse (RN) in the State of Georgia;
- Graduate from an accredited nursing program or Bachelor's degree;
- Minimum of one year of clinical research experience;
- Healthcare system software proficient;
- Microsoft Office Suite proficient;
- Experience with phlebotomy, specimen collection and processing;
- ARUP preparation and handling;
- IATA Packaging and Shipping Infectious Materials (or similar) certification or obtain one within 30 days of employment;
- Collaborative Institutional Training within 30 days of employment;
- Basic Life Support Certification or obtain one within 30 days of employment.
- Must be computer literate and able to operate various healthcare systems and multiple Microsoft Office applications.
- The ability to communicate with patients, visitors, co-workers, and physicians with courtesy and respect.
- Communicate clearly with patients and coworkers through the telephone, email, and in-person.
- Plan, prioritize, and complete multiple tasks as delegated.
- Displays a professional outgoing warm and helpful attitude.
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