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.
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, SCResponsible 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.
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.
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 (Walhalla, SC) SiteBridge Research, Inc.Clinical Research Coordinator (Walhalla, SC)Walhalla, SCFounded in 2021, SiteBridge Research (SBR) is an integrated research organization, building a national network of small and community practices to deliver world-class industry sponsored clinical research on time and on budget, accelerating time to market and product adoption in communities that are hardest to reach. The role involves close collaboration with the site team, sponsors, and clinical monitors to ensure ICH/GCP compliance, optimize site efficiency, and support timely study completion.
Clinical Research Coordinator (Walhalla, SC) SiteBridge Research IncClinical Research Coordinator (Walhalla, SC)Walhalla, SCSiteBridge Research Inc: Founded in 2021, SiteBridge Research (SBR) is an integrated research organization, building a national network of small and community practices to deliver world-class industry sponsored clinical research on time and on budget, accelerating time to market and product adoption in communities that are hardest to reach. The role involves close collaboration with the site team, sponsors, and clinical monitors to ensure ICH/GCP compliance, optimize site efficiency, and support timely study completion.
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.
Clinical Research Coordinator (Walhalla, SC) SiteBridge ResearchClinical Research Coordinator (Walhalla, SC)Walhalla, South CarolinaFounded in 2021, SiteBridge Research (SBR) is an integrated research organization, building a national network of small and community practices to deliver world-class industry sponsored clinical research on time and on budget, accelerating time to market and product adoption in communities that are hardest to reach. The role involves close collaboration with the site team, sponsors, and clinical monitors to ensure ICH/GCP compliance, optimize site efficiency, and support timely study completion.
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.
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 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.
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.
Research Assistant CLEMU Clemson UniversityResearch AssistantSeneca, South CarolinaThe position is a staff role in Clemson University's Institute for Engaged Aging, with a dynamic team dedicated to the Institute's mission to find and share the best ways to support and enrich the lives of older adults through research, education and community outreach. Responsible for: recruiting and screening older adult participants; administering informed consents, behavioral assessments, and study interventions; collecting, entering and analyzing data; ensuring compliance with all regulatory and reporting requirements; and possible outreach activities.
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.
IEA Research Lab Manager CLEMU Clemson UniversityIEA Research Lab ManagerSeneca, South CarolinaThis includes managing IRB approvals, preparing and maintaining federal, state, and university regulatory compliance documents, updating the protocol, study procedures, manuals of operations, related communications, data forms and other study documents, data collection, and coordinating and attending various study team meetings. 5% Ascend or descend (i.e. stairs, ladder): 5% Position self to accomplish task (i.e. stoop, kneel, crawl): 5% Communicate, converse, give direction, express oneself: 20% Recognize or inspect visually: 85% Move, transport, raise or lower 30lbs or less: 20% Extends hands or arms in any direction: 20% Perceive, observe, clarity of vision: 100% .
NewCorporate Trainee Program - Packaging Innovation & Consumer Research Intern Summer 2027 Quad/Graphics IncCorporate Trainee Program - Packaging Innovation & Consumer Research Intern Summer 2027Greenville, SCWe use our data-driven integrated marketing and manufacturing platform to streamline solutions for our clients, reduce friction and enhance their marketing spend effectiveness. Enrollment in a four-year Business, Communications, Graphic Communications, Marketing, Supply Chain, or related degree program.