NewRN Clinical Nurse Coordinator ER Fairview Park HospitalRN Clinical Nurse Coordinator ERDublin, GAIn collaboration with other members of the management team, the CNC directs, monitors, and evaluates nursing care in accordance with established policies/procedures, serves as a resource person for staff, and models a commitment to the organization’s vision/mission/values to support an unparalleled patient experience and clinical outcomes that contribute to overall departmental performance. Additional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-term care coverage, moving assistance, pet insurance and more.
NewRN Clinical Nurse Coordinator Telemetry Fairview Park HospitalRN Clinical Nurse Coordinator TelemetryDublin, GAIn collaboration with other members of the management team, the CNC directs, monitors, and evaluates nursing care in accordance with established policies/procedures, serves as a resource person for staff, and models a commitment to the organization’s vision/mission/values to support an unparalleled patient experience and clinical outcomes that contribute to overall departmental performance. The Clinical Nurse Coordinator (CNC) ensures and delivers high quality, patient-centered care and coordination of all functions in the unit/department during the designated shift.
Manager, Clinical Research Monitoring Edwards LifesciencesManager, Clinical Research MonitoringGeorgiaProviding input on strategic direction on field monitoring of studies and data collection for clinical trials with increased volume and complexity (e.g., KOL site), acting as a Core Team lead, assessing all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determining if clinical trial/study subject documentation is within parameters of study hypothesis, as well as monitoring clinical trial/study safety, in keeping with protocols, GCP (Good Clinical Practices) and regulatory requirements. Leading in the development of technical training on GCPs, protocols, database, compliance, device accountability, adverse event reporting, study investigation protocols, amendments, regulatory documentation requirements as well as training and proctoring new employees on trial and study related activities.
Registered Nurse Manager - Clinical Research - FT - Marietta WellstarRegistered Nurse Manager - Clinical Research - FT - MariettaGeorgiaEnsure appropriate orientation, education, credentialing, licensing, and continuing professional development for personnel, including study-specific training, GCP training and IATA certification. The Manager of the WellStar Research Institute is responsible for operations of the WellStar Research Institute including staff oversight and administration of HR functions.
RN Clinical Research - PRN Act for HealthRN Clinical Research - PRNGeorgiaWe are looking for CMRNs to visit an Adult population who can perform the following skills during a mobile visit: Blood specimen collection and processing (nurse will pick up dry ice prior to the visit and drop off at UPS after the visit). Two (2) years' experience in starting and performing Phlebotomy/Peripheral Blood Draw, IVs, and Subcutaneous Injections (date of last practice within 6 months, preferred).
Senior Specialist, Clinical Research Monitoring Edwards LifesciencesSenior Specialist, Clinical Research MonitoringGeorgiaField monitoring of studies and data collection for clinical trials, assessing all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determining if clinical trial/study subject documentation is within parameters of study hypothesis, as well as monitoring clinical trial/study safety, in keeping with protocols, GCP (Good Clinical Practices) and regulatory requirements. Developing and delivering technical training on GCPs, protocols, database, compliance, device accountability, adverse event reporting, study investigation protocols, amendments, regulatory documentation requirements as well as training and proctoring new employees on trial and study related activities.
Clinical Research Associate - Cross TA IREClinical Research Associate - Cross TAGeorgiaWilling and able to travel up to 50% for on-site monitoring visits across southeast region; preference given to candidates residing in Georgia near major HUB airports to support efficient regional travel. ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Inpatient Clinical Dietitian Advocate Health and Hospitals CorporationInpatient Clinical DietitianGeorgiaHeadquartered in Charlotte, North Carolina, Advocate Health services nearly 6 million patients and is engaged in hundreds of clinical trials and research studies, with Wake Forest University School of Medicine serving as the academic core of the enterprise. Assesses and monitors nutritional status of patients/clients and adjusts nutritional care as indicated utilizing current scientific literature on methodology and relates this information to medical status, anthropometric data, clinical assessment, and nutrition evaluation of the patient/client.
Area Clinical Manager - Full Time Affinity HospiceArea Clinical Manager - Full TimeGeorgiaActing as the regional counterpart to a Clinical Manager, this position also serves as interim clinical leadership at branch locations during Clinical Manager vacancies. The position requires extensive travel (approximately 90%) and the ability to sit in branch locations as needed to ensure operational stability, compliance, and continuity of leadership.
Clinical Affairs Scientist Agilent Technologies IncClinical Affairs ScientistGA$105,280–$197,400 / yearThe candidate will work directly with pharmaceutical partners, R&D scientists, Clinical Trial Managers/ Clinical Research Associates, Quality Assurance, and Regulatory Affairs to assure compliance with internal and external requirements. We are searching for an experienced Clinical Affairs Scientist (CAS) to work within the medical diagnostic field as a key member of the Organization of Chief Medical Officer (OCMO) Global Clinical Affairs team.
Validation Analyst/Senior Validation Analyst, Clinical Research Thermo Fisher Scientific IncValidation Analyst/Senior Validation Analyst, Clinical ResearchGARemote$75,800–$126,000 / yearAs a Senior Validation Analyst, you will play a critical role in the entire product development lifecycle by validating regulated computer systems used across the clinical research organization. At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy.
Senior Product Manager, Clinical Content NextGenSenior Product Manager, Clinical ContentGeorgiaFor this role, the portfolio is the company's ambulatory EHR and practice management platform, spanning the clinical documentation, ordering, e-prescribing, scheduling, patient access, and revenue cycle workflows that physician practices and ambulatory organizations depend on daily; the Senior Product Manager therefore pairs strong product craft with domain fluency in ambulatory care delivery and healthcare interoperability. Direct experience owning or contributing to ambulatory EHR and practice management products, with deep familiarity across the clinical and front/back-office workflows they support, including provider documentation, computerized order entry, e-prescribing (eRx/EPCS), clinical decision support, patient scheduling and registration, eligibility, and end-to-end revenue cycle management.
NewClinical Manager Home Health BrightSpring Health ServicesClinical Manager Home HealthDublin, GAAs a Home Health Clinical Manager, You will: Conducts/participates in quarterly quality improvement meetings, reviews pertinent available data, identifies trends, and oversees the implementation of improvement plans. Adoration Health, an affiliate of BrightSpring Health Services, provides quality and compassionate services in the comfort of home, providing support for patients, families, and caregivers in their time of need.
Clinical Review Coordinator, Women & Children's Advocate Health and Hospitals CorporationClinical Review Coordinator, Women & Children'sGeorgiaRemoteCoordinate local service line quality and outcomes improvement activities in partnership with physicians, advanced practice providers, nursing leaders, frontline teammates, quality leaders, and enterprise service line partners. This role requires a clinically strong RN who can effectively partner with physicians, advanced practice providers, nursing leaders, and frontline teams to identify improvement opportunities and lead data-driven performance improvement initiatives.
Clinical Specialist -South Georgia PROCEPT BioRobotics CorporationClinical Specialist -South GeorgiaGeorgiaIt continues with our one-of-a-kind management program designed to build the best managers in the industry, where our people managers across functions come together to exchange ideas and grow, as both managers and learners, in an environment that challenges, supports and broadens. It starts with our live induction program that serves as an incubator for cross-functional team building, an immersion in Procept’s history, jam-packed interactive sessions with executive leadership and a crash-course in the mission and purpose of what we do.
Clinical Coordinator - Facilities CMA, LPN, RN Your Health OrganizationClinical Coordinator - Facilities CMA, LPN, RNCochran, GAThis position involves proficient chart preparation, communication, scheduling of patient visits, appropriate utilization and logging of chronic care management activities, and provider and patient support. We are a leading physician group serving South Carolina and Georgia, dedicated to delivering quality healthcare directly to patients in care facilities, homes, clinics, and virtual visits.
Clinical Laboratory QA Coordinator Advocate Health and Hospitals CorporationClinical Laboratory QA CoordinatorGeorgiaBaccalaureate degree from an accredited college or university to include minimum of 30 quarter hours of lecture science, including at least 15 quarter hours of chemistry, 10 quarter hours of biology, and 5 quarter hours of mathematics (or equivalent semester hours). Headquartered in Charlotte, North Carolina, Advocate Health services nearly 6 million patients and is engaged in hundreds of clinical trials and research studies, with Wake Forest University School of Medicine serving as the academic core of the enterprise.
Collaborating Psychiatrist (Clinical & Supervisory Role) ThriveworksCollaborating Psychiatrist (Clinical & Supervisory Role)GeorgiaWith Job scams becoming more and more frequent, here's how to know you're speaking with a real member of our team: Our recruiters and other team members will only email you from thriveworks@myworkday.com or an @thriveworks.com email address. We are seeking a board-certified Psychiatrist to serve as a Collaborating Physician for our team of Psychiatric Mental Health Nurse Practitioners (PMHNPs), while also providing part-time direct psychiatric care to clients.
Clinical Director, BCBA Apollo BehaviorClinical Director, BCBAGeorgiaThis is a great opportunity for someone who wants to do great work with other excellent clinicians, be a part of a fun and collaborative culture, maintain work/life balance, and help implement the highest quality ABA available. Apollo Behavior is looking for a Clinical Director and Board Certified Behavior Analyst for our center-focused applied behavior analysis services in the Gainesville and Cumming Georgias area.
Clinical Research Associate II - Bilingual - US Southeast region - Multiple Therapeutic Areas Available Thermo Fisher Scientific IncClinical Research Associate II - Bilingual - US Southeast region - Multiple Therapeutic Areas AvailableGAActing as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability. Education and Experience Requirements: Bachelor's degree in a life science related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.