Registered Nurse (RN) Research, Clinical Research, FT, Days Prisma HealthRegistered Nurse (RN) Research, Clinical Research, FT, DaysGreenville, South CarolinaProvides patients/families with information regarding clinical trial participation and provides education regarding individual treatment including purpose, potential side effects, and self-care measures, documents interaction. Collaborates with the IRB of record and sponsoring agencies as well as local agencies, when applicable, to ensure global awareness regarding the progression of various studies, amendments and regulatory monitoring.
Clinical Research Coordinator II Velocity Clinical Research, Inc.Clinical Research Coordinator IIAnderson, South CarolinaTemporaryImplement and coordinate assigned clinical trials including start up, vendor management,subject recruitment, source development review, scheduling subjects, protocol training,collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports. Overview: Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites.
Clinical Research Coordinator I Velocity Clinical Research, Inc.Clinical Research Coordinator IAnderson, South CarolinaTemporaryCoordinate, with supervision, assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing, and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports. Overview: Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites.
NewClinical Research Coordinator II Velocity Clinical Research IncClinical Research Coordinator IIAnderson, SCImplement and coordinate assigned clinical trials including start up, vendor management,subject recruitment, source development review, scheduling subjects, protocol training,collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports. Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites.
Registered Nurse (RN) - Clinical Research - Oncology - St. Francis Cancer Center Bon Secours Mercy HealthRegistered Nurse (RN) - Clinical Research - Oncology - St. Francis Cancer CenterGreenville, South CarolinaEssential Job Functions : Enroll patients in research studies, associating visits / appointments / admissions with research studies and reviewing charges via the Research Billing Report to determine which are billed to Insurance and which are billed to the research study. Obtain required medical information from patients, advise patients of visits, assign numbers to the patients as required by protocol, and ensure that all study-related documentation, forms, CRF’s, are complete.
Registered Nurse (RN) - Clinical Research - Oncology - St. Francis Cancer Center Bon Secours Mercy Health IncRegistered Nurse (RN) - Clinical Research - Oncology - St. Francis Cancer CenterGreenville, SCEssential Job Functions: Enroll patients in research studies, associating visits / appointments / admissions with research studies and reviewing charges via the Research Billing Report to determine which are billed to Insurance and which are billed to the research study. Obtain required medical information from patients, advise patients of visits, assign numbers to the patients as required by protocol, and ensure that all study-related documentation, forms, CRF's, are complete.
Clinical Research Coordinator I Velocity Clinical Research IncClinical Research Coordinator IAnderson, SCCoordinate, with supervision, assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing, and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports. Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites.
Program Mgr-Non-Sponsored Clinical Research Spartanburg Regional Healthcare SystemProgram Mgr-Non-Sponsored Clinical ResearchSpartanburg, SCThe Manager of Clinical Research Program (Non-Sponsored) works closely with the Director of Clinical Research, Graduate Medical Education (GME) leadership, residency program directors, faculty mentors, Research Compliance, and health system leadership to develop and sustain a scalable model for resident/fellow research and quality improvement support. The manager oversees day-to-day operation of the resident research and QI support program, including workflow coordination, process development, and strategic planning to ensure consistent and high-quality support for resident-fellow scholarly activity and quality improvement work.
Program Mgr-Non-Sponsored Clinical Research Spartanburg Regional Medical CenterProgram Mgr-Non-Sponsored Clinical ResearchSpartanburg, SCThe Manager of Clinical Research Program (Non-Sponsored) works closely with the Director of Clinical Research, Graduate Medical Education (GME) leadership, residency program directors, faculty mentors, Research Compliance, and health system leadership to develop and sustain a scalable model for resident/fellow research and quality improvement support. The manager oversees day-to-day operation of the resident research and QI support program, including workflow coordination, process development, and strategic planning to ensure consistent and high-quality support for resident-fellow scholarly activity and quality improvement work.
Research Coordinator II, Administrative Research, Full Time, Days Prisma HealthResearch Coordinator II, Administrative Research, Full Time, DaysGreenville, South CarolinaCoordinates industry sponsored clinical trials by implementing sponsor provided protocols, completing required regulatory submissions, and ensuring adherence to study procedures and timelines. Responsible for the implementation and day-to-day management of clinical trial research studies, including educating research staff, health care team members, participants, and caregivers.
Research Coordinator II, Surgical Research, Full Time, Days Prisma HealthResearch Coordinator II, Surgical Research, Full Time, DaysGreenville, South CarolinaResponsible for the implementation, management and oversight of clinical trial research studies including the education of research staff, healthcare team member, participants and their caregivers. Coordinates industry sponsored clinical trials by implementing sponsor provided protocols, completing required regulatory submissions, and ensuring adherence to study procedures and timelines.
Research Coordinator II, Oncology, Full Time, Days Prisma HealthResearch Coordinator II, Oncology, Full Time, DaysGreenville, South CarolinaCoordinates industry sponsored clinical trials by implementing sponsor provided protocols, completing required regulatory submissions, and ensuring adherence to study procedures and timelines. Responsible for the implementation and day-to-day management of clinical trial research studies, including educating research staff, health care team members, participants, and caregivers.
IEA Research Lab Manager (Greenville, SC) CLEMU Clemson UniversityIEA Research Lab Manager (Greenville, SC)Greenville, South CarolinaBachelor of Science degree in medical technology, microbiology, biochemistry or a closely related field and relevant experience in a clinical or research laboratory environment. Military Equivalency : Clemson University is proud to allow educational equivalency for military technical certifications and trainings that directly relate to the job duties.
Research Specialist I (Part Time) - Department of Genetics and Biochemistry CLEMU Clemson UniversityResearch Specialist I (Part Time) - Department of Genetics and BiochemistryClemson, South Carolina45% - Assist in conducting computational analyses using AI and machine-learning models to infer gene regulation at the single-cell level and interpret complex biological datasets. Normal Operations - Required to follow emergency facility closure and modified operations directives, and not normally expected to work on-site during emergency situations.
MedTech Women's Health Procedural Specialist / Clinical Educator - East Coast IQVIA Holdings IncMedTech Women's Health Procedural Specialist / Clinical Educator - East CoastGreenville, SCIndividuals are typically required to have completed/up to date: Measles, Mumps & Rubella vaccine, Varicella (chicken pox) vaccine, Negative Tuberculosis (TB) Test, Tetanus, Diphtheria & Pertussis (Tdap) vaccine, Hepatitis B vaccine, Influenza vaccine (seasonal), and COVID-19 vaccine primary series. Our Women's Health Procedural Specialists experience a unique opportunity to leverage their clinical expertise while supporting healthcare providers through education and training on innovative women's health technologies.
Clinical RN Ii-Gibbs Patient Center Spartanburg Regional Medical CenterClinical RN Ii-Gibbs Patient CenterBatesville, SCCritically assesses assigned patients' medical history, admitting diagnosis and physician's orders, obtains nursing history, performs physical assessment, evaluates diagnostic data, and interviews patient and family to determine patient needs. The RN demonstrates thorough knowledge of therapeutic patient care, patient advocacy, clinical pathways/care maps, team dynamics, hospital systems, and serves as a resource for support associates.
Iach Research Assistant Furman UniversityIach Research AssistantGreenville, SCThe position will assist with research activities such as scheduling meetings and taking meeting minutes, IRB submission and amendments, literature reviews, data collection, data cleaning, descriptive data analysis, and reporting. Relationships: Continuous contact with members of own work unit to plan, coordinate, problem solve, exchange information, and make suggestions related to mutual and institutional goals.
IACH Research Assistant Furman UniversityIACH Research AssistantSCThe position will assist with research activities such as scheduling meetings and taking meeting minutes, IRB submission and amendments, literature reviews, data collection, data cleaning, descriptive data analysis, and reporting. Relationships: Continuous contact with members of own work unit to plan, coordinate, problem solve, exchange information, and make suggestions related to mutual and institutional goals.
NewRegistered Dietitian, Clinical Nutrition, PRN, Day Prisma HealthRegistered Dietitian, Clinical Nutrition, PRN, DayGreenville, South CarolinaEvaluates patients' nutritional status, develop and implement care plans, assess nutrient requirements, recommends nutrition prescriptions, evaluates patient tolerance and effectiveness, as well as communicates information to physicians and other health care professionals. If hired on or prior to December 31, 2023, must have a minimum of a Bachelor's degree in nutrition or dietetics AND Credentialed as a Registered Dietitian by the Commission on Dietetic Registration (CDR).
Pharmacy Clinical Specialist SiteLabsPharmacy Clinical SpecialistClemson, SC$55,000–$70,000 / yearYou will work both in person and virtually, traveling to pharmacy locations to stand up programs and train staff, then supporting pharmacies remotely through virtual check-ins, performance monitoring, and data-driven coaching. SiteLabs is an early-stage, technology-forward company transforming independent pharmacies into trusted community access points for wellness screenings, clinical trials, and patient navigation.