Research Nurse Coordinator, RN (58011) Position Available In DeKalb, Georgia
Tallo's Job Summary: The Research Nurse Coordinator, RN (58011) at United Digestive is responsible for providing clinical and administrative nursing support for research trials and studies. The role involves patient recruitment, data collection, patient care, and adherence to GCP guidelines. Requirements include RN licensure, clinical research experience, and proficiency in healthcare software and Microsoft Office Suite. Travel may be required. United Digestive is an Equal Opportunity Employer with a drug-free workplace policy.
Job Description
Job Description:
DescriptionJob Title:
Research Nurse CoordinatorReports To:
Clinical Research ManagerDepartment:
Ancillary ServicesOfficeSetting:
In OfficeFLSA Status:
Non ExemptPay Type:
HourlySummary
GENERAL SUMMARY OF DUTIES
:
United Digestive’s (UD)Research Nurse Coordinator is responsible for assisting theClinical Research Department and principal Investigators with allclinical and organizational tasks , aligning with clinical trialprocedures and protocol requirements. The Research NurseCoordinator is expected to provide clinical and administrativenursing support for research trials, studies, and projects. TheClinical Research Nurse is expected to exhibit basic knowledge ofclinical research activities and support clinical research trialsbased on the needs of the research department. The ClinicalResearch Nurse should adhere to and have a strong understanding ofGood Clinical Practice (GCP) guidelines and regulatoryrequirements.
ResponsibilitiesDuties include but are not limitedto: Recruits and screens potential patients and obtains informedconsent. Assists in providing patient education including benefits andrisks of participating in a clinical trial Follows clinical trial protocols to accurately and efficientlycollect and document participant data including, but not limitedto, laboratory collection and processing, vital assessments, andstudy-specific procedures Provides direct nursing care according to UD’s standards ofpractice. Administers investigational product (IP) per clinical trialprotocol requirements. Completes clinical assessments and safety evaluations of studysubjects and notifies study principal Investigator and Sponsor andstudy team per reporting guidelines. Maintains data management per study requirements andcontractual obligations. Completes required study trainings and maintains strongknowledge of clinical and research protocols. Maintains equipment and supply resources for researchstudies. Performs upkeep of exam and work rooms with regard tosterilization, infection control, supplies, and equipment. Follows all CLIA Patient Safety Goals, including observingstrict infectious disease precautions when handling blood specimensand IATA for specimen shipment. Answers emails, voicemails, and returns patient calls in atimely and efficient, and professional manner. Work with internal teams to ensure patients are properlycompensated for visits completed per study schedule by documentingappropriate procedure completion. Abides by and promotes HIPAA compliance; maintains strictestconfidentiality. Participates in staff meetings as directed by the principalinvestigators and Clinical Research Manager. Cross trains and performs other functions as directed by theprincipal investigators and Clinical Research Manager. Any other duties and/or special projects as assigned within theresearch department. Maintains strong relationships with Principal Investigator andSub-Investigators on assigned studies Assists other Clinical Research Coordinators and ClinicalResearch Nurses on study visits as backup coordinator when requiredand able per delegation of authority logs. Performs any other duties and/or special projects asassigned
Education, Skills, & Experience Required:
Licensure as a Registered Nurse (RN) in the State ofGeorgia; Graduate from an accredited nursing program or Bachelor’sdegree; Minimum of one year of clinical research experience; Healthcare system software proficient; Microsoft Office Suite proficient; Experience with phlebotomy, specimen collection andprocessing; 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 ofemployment; Basic Life Support Certification or obtain one within 30 daysof employment.
Core Skills At United DigestiveThe Clinical ResearchCoordinator must have or be able to: Must be computer literate and able to operate varioushealthcare 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 thetelephone, email, and in-person. Plan, prioritize, and complete multiple tasks asdelegated. Displays a professional outgoing warm and helpfulattitude.
Physical/Mental/Environmental DemandsRequires sitting andstanding associated with a normal office environment. Travelrequired as business needs dictate.
Drug Free WorkplaceUnitedDigestive is a drug-free workplace. All offers of employment arecontingent upon passing a pre-employment drug screening.
EqualOpportunity EmployerUnited Digestive is an Equal OpportunityEmployer and does not discriminate on the basis of race, religion,gender, color, or national origin in its employment practices.