Clinical Research Associate (CRA II/Senior) - Metabolic - US Any Region Parexel International CorpClinical Research Associate (CRA II/Senior) - Metabolic - US Any RegionSCWith 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere. As a CRA, you will manage clinical sites from identification through closeout, serving as the primary point of contact for site teams and helping ensure study quality, patient safety, regulatory compliance, and accurate clinical data.
Clinical Research Associate (CRA II/Senior) - Ophthalmology - US Any Region Parexel International CorpClinical Research Associate (CRA II/Senior) - Ophthalmology - US Any RegionSCWith 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere. As a CRA, you will manage clinical sites from identification through closeout, serving as the primary point of contact for site teams and helping ensure study quality, patient safety, regulatory compliance, and accurate clinical data.
Clinical Research Associate (CRA II/Senior) - Oncology - US Any Region Parexel International CorpClinical Research Associate (CRA II/Senior) - Oncology - US Any RegionSCWith 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere. As a CRA, you will manage clinical sites from identification through closeout, serving as the primary point of contact for site teams and helping ensure study quality, patient safety, regulatory compliance, and accurate clinical data.
UNIV - Clinical Research Sponsor Invoicing Analyst - Office of Clinical Research, OVPR MUSCUNIV - Clinical Research Sponsor Invoicing Analyst - Office of Clinical Research, OVPRSouth CarolinaIn collaboration with department/division Grants Administrators, Principal Investigators and study teams, Research Administration and Grants and Contracts Accounting Offices, this position will coordinate industry sponsored study invoicing, billing and reconciliation activities to ensure that all earned revenue is realized under this OCR fee for service program and provide training, mentorship and guidance for sponsor invoicing within MUSC’s Clinical Trial Management System. Experience as a clinical research coordinator, research nurse coordinator, research/sponsored programs accountant, grants administrator, or professional accountant/financial analyst with direct industry sponsored research experience preferred, or an equivalent combination of experience, education and training.
UNIV - Clinical Research Sponsor Invoicing Analyst - Office of Clinical Research, OVPR Medical University of South CarolinaUNIV - Clinical Research Sponsor Invoicing Analyst - Office of Clinical Research, OVPRSouth CarolinaIn collaboration with department/division Grants Administrators, Principal Investigators and study teams, Research Administration and Grants and Contracts Accounting Offices, this position will coordinate industry sponsored study invoicing, billing and reconciliation activities to ensure that all earned revenue is realized under this OCR fee for service program and provide training, mentorship and guidance for sponsor invoicing within MUSC’s Clinical Trial Management System. Experience as a clinical research coordinator, research nurse coordinator, research/sponsored programs accountant, grants administrator, or professional accountant/financial analyst with direct industry sponsored research experience preferred, or an equivalent combination of experience, education and training.
Senior Clinical Research Associate - CNS - Southeast (Remote) Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - CNS - Southeast (Remote)SCRemote$97,000–$193,000 / yearTypically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.
Senior Clinical Research Associate - Psychiatry - Southeast Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - Psychiatry - SoutheastSC$97,000–$193,000 / yearTypically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.
Senior Clinical Research Associate - CNS - Southeast Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - CNS - SoutheastSC$97,000–$193,000 / yearTypically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.
FSP Clinical Research Associate 2 Fortrea IncFSP Clinical Research Associate 2SCRemote$100,000–$112,000 / yearResponsibilities: Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.
NewUNIV - CTMS Reporting Program Manager - Office of Clinical Research, OVPR MUSCUNIV - CTMS Reporting Program Manager - Office of Clinical Research, OVPRSouth CarolinaIntegrate, validate, and reconcile data from multiple systems to meet enterprise reporting and analytics needs, including combining OnCore invoice and payment records with Workday financial data to support reporting on invoiced revenue, payments received, outstanding balances, reconciliation status, and clinical trial financial performance. This position collaborates with OCR leadership and staff, investigators, study teams, research administrators, and technical teams to develop meaningful dashboards, reports, and performance indicators that support optimized research activation, participant accrual, data entry timeliness, financial performance, compliance, and overall research operations.
NewUNIV - CTMS Reporting Program Manager - Office of Clinical Research, OVPR Medical University of South CarolinaUNIV - CTMS Reporting Program Manager - Office of Clinical Research, OVPRSouth CarolinaIntegrate, validate, and reconcile data from multiple systems to meet enterprise reporting and analytics needs, including combining OnCore invoice and payment records with Workday financial data to support reporting on invoiced revenue, payments received, outstanding balances, reconciliation status, and clinical trial financial performance. This position collaborates with OCR leadership and staff, investigators, study teams, research administrators, and technical teams to develop meaningful dashboards, reports, and performance indicators that support optimized research activation, participant accrual, data entry timeliness, financial performance, compliance, and overall research operations.
Research Coordinator Midlands Neurology and Pain Associates, P.A.Research CoordinatorColumbia, South CarolinaYou will work closely with our Principal Investigators (PIs), clinical staff, and industry sponsors to ensure that all research is conducted with the highest degree of integrity, compliance, and patient safety. Seeking a highly organized, detail-oriented Clinical Research Coordinator to join our team and bridge the gap between innovative medical research and compassionate patient care.
NewResearch Specialist University of South CarolinaResearch SpecialistColumbia, SCLogo Posting Number TMP02029PO26 Job Code Title Research Specialist I Advertised Title Research Specialist Campus Columbia College/Division Arnold School of Public Health Department ASPH Communication Sciences and Disorders Salary Commensurate with experience Location of Vacancy Part/Full Time Part Time Hours per Week 10 Work Schedule. The research specialist will work with the faculty principal investigator and grant staff to assist with NIH-funded research by conducting assessments on early development in children with neurodevelopmental conditions (e.g., Down syndrome) using multiple developmental, physiological, behavioral, and sensorimotor measures.
Research Specialist State of South CarolinaResearch SpecialistRichland County, SCIn addition, our Palmetto College campuses in Salkehatchie, Union, Lancaster and Sumter enable students to earn associate or bachelors degrees through a combination of in-person, online or blended learning. More than 50,000 students are enrolled at one of eight institutions, including the research campus in Columbia and comprehensive four-year universities in Aiken, Upstate and Beaufort.
Internship (Columbia Research) US Oncology IncInternship (Columbia Research)Columbia, SCCookies are used on this site to assist in continually improving the candidate experience and all the interaction data we store of our visitors is anonymous. We're sorry, but it looks like this job may be no longer available or does not exist.
Resource Nurse (RN) / Non-Institutional / Education, Training & Research (ETR) State of South CarolinaResource Nurse (RN) / Non-Institutional / Education, Training & Research (ETR)Richland County, SC$70,455–$89,800 / yearAs the Resource Nurse, working under the supervision of the Director of Education, Training and Research (ETR), plan, provide and evaluate educational programs for the staff of South Carolina Department of Behavioral Health and Developmental Disabilities - Office of Mental Health (BHDD-OMH). This position is located at the SC Department of Behavioral Health and Developmental Disabilities (DBHDD) - Office of Mental Health-Education, Training and Research (ETR) Division- Crafts-Farrow State Hospital, Building 3, 7901 Farrow Road, Columbia, SC 29203.
UNIV - Senior Data Architect, Research Analytics - Department of SCTR MUSCUNIV - Senior Data Architect, Research Analytics - Department of SCTRSouth CarolinaThe Senior Data Architect, Research Analytics will lead the South Carolina Clinical and Translational Science (SCTR) Institute’s data and reporting strategy and will engage with enterprise IS data leadership and teams to strategize for the design, creation, refinement, and long-term sustainability of an enterprise research data repository that integrates and curates' data from multiple disparate systems across the research lifecycle. The Senior Data Architect, Research Analytics will lead the South Carolina Clinical and Translational Science (SCTR) Institute’s data and reporting strategy and will engage with enterprise IS data leadership and teams to strategize for the design, creation, refinement, and long-term sustainability of an enterprise research data repository that integrates and curates data from multiple disparate systems across the research lifecycle.
UNIV - Senior Data Architect, Research Analytics - Department of SCTR Medical University of South CarolinaUNIV - Senior Data Architect, Research Analytics - Department of SCTRSouth CarolinaThe Senior Data Architect, Research Analytics will lead the South Carolina Clinical and Translational Science (SCTR) Institute’s data and reporting strategy and will engage with enterprise IS data leadership and teams to strategize for the design, creation, refinement, and long-term sustainability of an enterprise research data repository that integrates and curates' data from multiple disparate systems across the research lifecycle. The Senior Data Architect, Research Analytics will lead the South Carolina Clinical and Translational Science (SCTR) Institute’s data and reporting strategy and will engage with enterprise IS data leadership and teams to strategize for the design, creation, refinement, and long-term sustainability of an enterprise research data repository that integrates and curates data from multiple disparate systems across the research lifecycle.
NewAssociate Clinical Experience (ACE) Intern - Summer 2027 Medtronic PlcAssociate Clinical Experience (ACE) Intern - Summer 2027SCThe following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program). If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
MedTech Women's Health Procedural Specialist / Clinical Educator - East Coast IQVIA Holdings IncMedTech Women's Health Procedural Specialist / Clinical Educator - East CoastColumbia, 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.