South Carolina Psychiatry Leadership Position – Assistant/Associate Program Director The Medicus FirmSouth Carolina Psychiatry Leadership Position – Assistant/Associate Program DirectorFlorence, SCp style="text-align:center">Seeking a dynamicAPDto launch and lead a newCommunity Psychiatry Residency Programat the state-of-the-art behavioral health facility. Outdoor Recreation Year-Round- Access to parks, golf courses, and nearby lakes, plus close proximity to South Carolinas coast for weekend getaways.
Senior Clinical Research Associate ICON PlcSenior Clinical Research AssociateBlue Bell, SCFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Senior Clinical Research Associate IRESenior Clinical Research AssociateSouth CarolinaICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Clinical Research Coordinator, Oncology Research, Full Time, Days Prisma HealthClinical Research Coordinator, Oncology Research, Full Time, DaysGreenville, SCExperience - Two (2) years of Allied health, medical or research related experience In Lieu Of In lieu of education and experience noted above, equivalent combination of work/academic experience may be considered (i.e., Bachelor's degree in clinical, healthcare or scientific related field of study) Required Certifications, Registrations, Licenses SoCRA or ACRP certification - Preferred Oncology medical research experience - Preferred Some medical office experience preferable in oncology - Preferred Knowledge, Skills and Abilities Computer skills (word processing, spreadsheets, database, data entry) Medical terminology knowledge - Preferred Work Shift Day (United States of America) Location Cancer Centers - Faris Road Facility 1008 Greenville Memorial Hospital Department 10559220 OP Oncology Research-CIF Share your talent with us! Compiles medical records of research subjects during the on-study, treatment and follow-up periods and reports required elements to the research sponsor in a complete, accurate and timely manner.
Clinical Research Coordinator - Spartanburg, SC Advanced Dermatology & Cosmetic SurgeryClinical Research Coordinator - Spartanburg, SCSpartanburg, SCCompletes study documentation and maintains study files in accordance with sponsor requirements including, but not limited to, consent forms, source documentation, and note to file, case report forms, and investigational material accountability forms. ESSENTIAL DUTIES AND RESPONSIBILITIES: Coordinates with Principal Investigator, department, and administration to help ensure that clinical research and related activities are performed in accordance with Federal Regulations and sponsoring agency (pharmaceutical and or CRO) policies and procedures.
Clinical Research Coordinator I Velocity Clinical Research, Inc.Clinical Research Coordinator IUnion, South CarolinaCoordinate, 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.
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, OVPRCharleston, SC$52,100–$70,300 / yearIn 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 MUSCs Clinical Trial Management System. In 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.
Clinical Research Coordinator Alcanza Clinical Research LLCClinical Research CoordinatorNorth Charleston, SCResponsibilities may include but are not limited to: • Screening of patients for study enrollment • Patient consents • Patient follow-up visits • Documenting in source clinic charts • Entering data in EDC and answering queries • Obtaining vital signs and ECGs • May perform basic lab procedures per protocol such as blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens, and notification of courier for specimen pick-up • Requesting and tracking medical record requests • Updating and maintaining logs, chart filings • Maintaining & ordering study specific supplies • Scheduling subjects for study visits and conducts appointment reminders • Building, updating source as needed • Conducting monitoring visits and resolves issues as needed in a timely manner • Ensuring study related reports and patient results are reviewed by investigator in a timely manner • Filing SAE • Deviation reports to Sponsor and IRB as needed • Documenting and reporting adverse events • Reporting non-compliance to appropriate staff in timely manner • Maintaining positive and effective communication with clients and team members • Always practicing ALCOAC principles with all documentation • May assist with study recruitment, patient enrollment, and tracking as needed • Maintaining confidentiality of patients, customers, and company information • Performing all other duties as requested or assigned • Complete all needed activities for study start-up including completing required training, uploading printing certificates to file in ISF, etc. A Medical Assistant diploma, LPN, VN, EMT credential, or Associates degree AND a minimum of 1 year of clinical research or clinical experience OR an equivalent combination of education and experience is required.
NewClinical Research Coordinator Actalent IncClinical Research CoordinatorSpartanburg, SC$27–$32 / hourli>Ability to interact daily with physicians, nurses, study monitors and other sponsor representatives, administrators and other employees, community resources, patients and their families and significant others. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service.
Clinical Research Coordinator Alcanza Clinical ResearchClinical Research CoordinatorCharleston, South CarolinaScheduling subjects for study visits and conducts appointment reminders; Building/updating source as needed; Conducting monitoring visits and resolves issues as needed in a timely manner; Ensuring study related reports and patient results are reviewed by investigator in a timely manner; Filing SAE/Deviation reports to Sponsor and IRB as needed; Documenting and reporting adverse events; Reporting non-compliance to appropriate staff in timely manner; Maintaining positive and effective communication with clients and team members; Always practicing ALCOAC principles with all documentation; May assist with study recruitment, patient enrollment, and tracking as needed; Maintaining confidentiality of patients, customers and company information, and; Performing all other duties as requested or assigned. Responsibilities may include but are not limited to:Screening of patients for study enrollment; Patient consents; Patient follow-up visits; Documenting in source clinic charts; Entering data in EDC and answers queries; Obtaining vital signs and ECGs; May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; Requesting and tracking medical record requests; Updating and maintaining logs, chart filings; Maintaining & ordering study specific supplies;].
Clinical Research Coordinator I Velocity Clinical Research IncClinical Research Coordinator IThompson, 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.
Nurse Practitioner or Physician Assistant - Clinical Research Headlands Research IncNurse Practitioner or Physician Assistant - Clinical ResearchMyrtle Beach, SCQualifications: Minimum of two years of experience as a licensed physician assistant, family or non-acute adult nurse practitioner treating a wide variety of therapeutic areas for the adult and geriatric patient population required (internal medicine, family medicine, urgent care, emergency medicine). Dynamic Team Environment: You'll help Headlands Research continue to build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists.
Nurse Practitioner or Physician Assistant - Clinical Research Headlands ResearchNurse Practitioner or Physician Assistant - Clinical ResearchMyrtle Beach, South CarolinaMinimum of two years of experience as a licensed physician assistant, family or non-acute adult nurse practitioner treating a wide variety of therapeutic areas for the adult and geriatric patient population required (internal medicine, family medicine, urgent care, emergency medicine). Dynamic Team Environment: You'll help Headlands Research continue to build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists.
Clinical Research Coordinator (Clemson, SC) SiteBridge Research, Inc.Clinical Research Coordinator (Clemson, SC)Clemson, 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 I (Temp Position Tentatively July 20, 2026 July 20, 2027) Shriners Hospitals for ChildrenClinical Research Coordinator I (Temp Position Tentatively July 20, 2026 July 20, 2027)Greenville, SCEmployees in a FT or PT status (40+ hours per pay period) will also be eligible for paid time off, life insurance, short term and long-term disability and the Flexible Spending Account (FSA) plans and a Health Savings Account (HSA) if a High Deductible Health Plan (HDHP) is elected. Greenville, South Carolina has been named among American's Best Small Cities by Condé Nast Traveler and one of the South's Best Cities on the Rise by Southern Living.
Clinical Research Patient Recruitment Supervisor Alcanza Clinical Research LLCClinical Research Patient Recruitment SupervisorNorth Charleston, SCOversee assigned staff scheduling to ensure optimal site-based recruitment activity, coverage, payroll timecards, absence tracking/approvals, new hire orientation and training per operational needs. Oversee people management activities for assigned team, including participation with interviewing, completing performance appraisals, engaging with employee counseling, career coaching and, when needed, and other employment related meetings.
NewClinical Research Coordinator (Clemson, SC) SiteBridge Research IncClinical Research Coordinator (Clemson, SC)Clemson, SCp>SiteBridge 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 Patient Recruitment Supervisor Alcanza Clinical ResearchClinical Research Patient Recruitment SupervisorCharleston, South CarolinaOversee assigned staff scheduling to ensure optimal site-based recruitment activity, coverage, payroll timecards, absence tracking/approvals, new hire orientation and training per operational needs. Oversee people management activities for assigned team, including participation with interviewing, completing performance appraisals, engaging with employee counseling, career coaching and, when needed, and other employment related meetings.
Registered Nurse (RN) - Clinical Research - Upstate Cardiology Bon Secours Mercy HealthRegistered Nurse (RN) - Clinical Research - Upstate CardiologyGreenville, South CarolinaPrimary responsibilities include recruiting and monitoring study participants, maintaining research materials required for coordinating projects, protocol compliance, assisting research investigators in developing and completing research projects. Bon Secours seeks people that are committed to our values of compassion, human dignity, integrity, service and stewardship to create an environment where associates want to work and help communities thrive.
Clinical Research Coordinator I ObjectiveHealth IncClinical Research Coordinator IIndian Land, SCNot easily distracted: You have the ability to stay focused while running different protocols, resolving and submitting IRB responses and audit findings, tracking AE and SAE events, and maintaining eSource material for assigned studies. ObjectiveHealth is a clinical research company that uses proprietary technology to: Increase patient access to research trials within our communities, Provide physicians with enhanced care options for current patients, and.
Lead Clinical Research Coordinator Actalent IncLead Clinical Research CoordinatorGreenville, SC$27–$32 / hourWe are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
NewUNIV - Clinical Research Coordinator - Department of Medicine: Division of Pulmonary MUSCUNIV - Clinical Research Coordinator - Department of Medicine: Division of PulmonaryCharleston, South CarolinaResponsibilities include (but not limited to) obtaining informed consent, coordinating, and scheduling study visits, educating participants about study procedures, monitoring and reporting adverse events (including preparation of serious adverse event reports), collecting and processing laboratory specimens, dispensing investigational products, reviewing patient diaries, completing required study procedures, entering data, and completing case report forms, and maintaining accurate and compliant study documentation. Responsibilities include collecting, recording, and submitting study data within required timelines; providing database support (design, implementation, updates, and integrity review); extracting data from Epic; and responding to and resolving data queries promptly to ensure accuracy and compliance.
UNIV - Clinical Research Coordinator - Department of Medicine: Division of Pulmonary Medical University of South CarolinaUNIV - Clinical Research Coordinator - Department of Medicine: Division of PulmonaryCharleston, South CarolinaResponsibilities include (but not limited to) obtaining informed consent, coordinating, and scheduling study visits, educating participants about study procedures, monitoring and reporting adverse events (including preparation of serious adverse event reports), collecting and processing laboratory specimens, dispensing investigational products, reviewing patient diaries, completing required study procedures, entering data, and completing case report forms, and maintaining accurate and compliant study documentation. Responsibilities include collecting, recording, and submitting study data within required timelines; providing database support (design, implementation, updates, and integrity review); extracting data from Epic; and responding to and resolving data queries promptly to ensure accuracy and compliance.
Clinical Research Coordinator I (Temp Position Tentatively July 20, 2026-July 20, 2027) Shriners Children'sClinical Research Coordinator I (Temp Position Tentatively July 20, 2026-July 20, 2027)Greenville, South CarolinaEmployees in a FT or PT status (40+ hours per pay period) will also be eligible for paid time off, life insurance, short term and long-term disability and the Flexible Spending Account (FSA) plans and a Health Savings Account (HSA) if a High Deductible Health Plan (HDHP) is elected. Greenville, South Carolina has been named among American’s Best Small Cities by Condé Nast Traveler and one of the South’s Best Cities on the Rise by Southern Living.
Registered Nurse (RN) - Clinical Research - Upstate Cardiology Bon Secours Mercy Health IncRegistered Nurse (RN) - Clinical Research - Upstate CardiologyGreenville, SCPrimary responsibilities include recruiting and monitoring study participants, maintaining research materials required for coordinating projects, protocol compliance, assisting research investigators in developing and completing research projects. Bon Secours seeks people that are committed to our values of compassion, human dignity, integrity, service and stewardship to create an environment where associates want to work and help communities thrive.
Clinical Assistant or Clinical Associate Professor University of South CarolinaClinical Assistant or Clinical Associate ProfessorColumbia, SCThe successful candidate must have a Registered Dietitian/Registered Dietician Nutritionist (RD/RDN) credential, graduate degree (minimum of a master's degree) in nutrition, dietetics, exercise science or health-related field by the start date of employment August 16, 2026, experience teaching/mentoring in a higher education setting, a history of post-credentialing professional dietetics experience (5+ years with a master degree, 3+ years with a doctoral degree), and relevant exercise, human performance, or nutrition experience. The Program Director will be responsible for all aspects of academic leadership and administration within the MS/PND program, including maintaining accreditation status; providing mentorship and faculty/preceptor development; monitoring and evaluating the curriculum; monitoring and evaluating program and learning assessment measures; chairing the program committees; and participating in scholarship and service.
Clinical Assistant or Clinical Associate Professor State of South CarolinaClinical Assistant or Clinical Associate ProfessorRichland County, SCp>The successful candidate must have a Registered Dietitian/Registered Dietician Nutritionist (RD/RDN ) credential, graduate degree (minimum of a masters degree) in nutrition, dietetics, exercise science or health-related field by the start date of employment August 16, 2026, experience teaching/mentoring in a higher education setting, a history of post-credentialing professional dietetics experience (5+ years with a master degree, 3+ years with a doctoral degree), and relevant exercise, human performance, or nutrition experience. The Department of Exercise Science at the University of South Carolina (USC ) Arnold School of Public Health (ASPH http://www.sph.sc.edu/invites applications for a Clinical Assistant or Clinical Associate Professor position focused on directing our Master of Science in Performance Nutrition and Dietetics (MS/PND ) degree program.
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.
Associate Director of Projects -Clinical Affairs State of South CarolinaAssociate Director of Projects -Clinical AffairsRichland County, SCClickhttps://nam02.safelinks.protection.outlook.com/?url=https%3A%2F%2Fsc.edu%2Fabout%2Foffices_and_divisions%2Fhuman_resources%2Fcareers%2Findex.php&data=05%7C01%7CKURTRS%40email.sc.edu%7Ceca45df616784275e15908dab2a706ac%7C4b2a4b19d135420e8bb2b1cd238998cc%7C0%7C0%7C638018727680845870%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=j6sQGvabHDZHDmRBFwMrq8P8QCuDmChuJ%2FH5%2F8hDRUw%3D&reserved=0 to learn more about why you should work at USC . The role is responsible for establishing disciplined project governance, operational readiness, stakeholder alignment, and enterprise-wide coordination across a dynamic portfolio of initiatives, including the development and activation of the University of South Carolina Neurological Hospital, the Brain Health Network, and future clinical innovation programs.
Associate Director of Projects -Clinical Affairs University of South CarolinaAssociate Director of Projects -Clinical AffairsColumbia, SCLogo Posting Number STA00430PO26 Job Family Operational Analysis Job Function Project Management USC Market Title Aso Dir of Projects, Clinical Affairs Link to USC Market Title https://uscjobs.sc.edu/titles/206843 Job Level P4 - Professional Business Title (Internal Title) Associate Director of Projects -Clinical Affairs Campus Columbia Work County Richland College/Division Neurological Critical Care Hospital Department NCCH Neurological Hospital SCHHS State Pay Range Unclassified USC Market Range MRN - $120,769 $153,981 $187,192 Anticipated Hiring Range Salary commensurate with qualifications Location of Vacancy Part/Full Time Full Time Hours per Week 37.5 Work Schedule. The role is responsible for establishing disciplined project governance, operational readiness, stakeholder alignment, and enterprise-wide coordination across a dynamic portfolio of initiatives, including the development and activation of the University of South Carolina Neurological Hospital, the Brain Health Network, and future clinical innovation programs.
Open Rank-Clinical (Assistant Prof., Associate Prof., Professor) University of South CarolinaOpen Rank-Clinical (Assistant Prof., Associate Prof., Professor)Columbia, SCp>Benefits for FTE Positions The University of South Carolina, USC, through the State of SC and Public Employee Benefit Authority (PEBA), offers state employees a valuable benefits package, including health and life insurance, generous paid leave, and retirement programs. In 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.
NewUNIV - Research Study Coordinator-Hollings Cancer Center MUSCUNIV - Research Study Coordinator-Hollings Cancer CenterCharleston, South CarolinaUnder general supervision of the Clinical Trials Office (CTO) and specific disease group Program Manager within the Clinical Operations Unit, this position coordinates, establishes, and supervises complex research protocols at the Hollings Cancer Center (HCC) to efficiently and effectively integrate the National Cancer Institute (NCI), investigator initiated and industry sponsored oncology trials at the Medical University of South Carolina (MUSC). Under guidance of the team lead coordinator(s) and program manager, will support research activities at any of the MUSC main campus and HCC satellite locations and make necessary coverage plans in advance, to avoid interruption of quality CTO services.
NewUNIV - Research Study Coordinator-Hollings Cancer Center Medical University of South CarolinaUNIV - Research Study Coordinator-Hollings Cancer CenterCharleston, SCp>Summary: Under general supervision of the Clinical Trials Office (CTO) and specific disease group Program Manager within the Clinical Operations Unit, this position coordinates, establishes, and supervises complex research protocols at the Hollings Cancer Center (HCC) to efficiently and effectively integrate the National Cancer Institute (NCI), investigator initiated and industry sponsored oncology trials at the Medical University of South Carolina (MUSC). Under guidance of the team lead coordinator(s) and program manager, will support research activities at any of the MUSC main campus and HCC satellite locations and make necessary coverage plans in advance, to avoid interruption of quality CTO services.
Research Program Coordinator I University of South CarolinaResearch Program Coordinator IColumbia, SCp>Position Description Advertised Job Summary Community Health Worker will work with licensed research nurse RN and other team members to assist in coordinating and delivering a telehealth/remote intervention with patients with chronic health conditions, as well as their Carepartners for a research study funded by the National Institutes of Health (NIH) that seeks to improve current and future chronic illness management among adults and their caregivers in medically underserved and rural areas of South Carolina. Ability to work with a level of independence and also in concert with the research team, patients, and their respective care partners to operationalize the devised wellness goals/plans by providing resource navigation, coordination, referral assistance, and facilitating access to care and other community resources.
UNIV - Program Manager I – EP, Structural & Preventative Cardiology Clinical Trials - Department of Medicine: Division of Cardiology MUSCUNIV - Program Manager I – EP, Structural & Preventative Cardiology Clinical Trials - Department of Medicine: Division of CardiologyCharleston, South CarolinaResponsible for ensuring adherence to study guidelines, managing the subject recruitment and informed consent process, providing education to patients and their families, and serving as the primary point of contact for study subjects. Participate in the feasibility review process by reviewing protocols and determining the study patient visit flow and provision of center resources to promote protocol compliance and study participant retention.
UNIV - Program Manager I - EP, Structural & Preventative Cardiology Clinical Trials - Department of Medicine: Division of Cardiology Medical University of South CarolinaUNIV - Program Manager I - EP, Structural & Preventative Cardiology Clinical Trials - Department of Medicine: Division of CardiologyCharleston, SCJob Duties: 35% - Supervision and Management of Research Staff: Responsible for the direct supervision of Cardiology Clinical Research staff (program coordinators, research assistants, etc.) that support clinical trials within the Heart Failure program. Responsible for ensuring adherence to study guidelines, managing the subject recruitment and informed consent process, providing education to patients and their families, and serving as the primary point of contact for study subjects.
UNIV - Program Manager I – Clinical Trials, Heart Failure - Department of Medicine: Division of Cardiology Medical University of South CarolinaUNIV - Program Manager I – Clinical Trials, Heart Failure - Department of Medicine: Division of CardiologyCharleston, South CarolinaResponsible for ensuring adherence to study guidelines, managing the subject recruitment and informed consent process, providing education to patients and their families, and serving as the primary point of contact for study subjects. Participate in the feasibility review process by reviewing protocols and determining the study patient visit flow and provision of center resources to promote protocol compliance and study participant retention.
UNIV - Program Manager I – Clinical Trials, Heart Failure - Department of Medicine: Division of Cardiology MUSCUNIV - Program Manager I – Clinical Trials, Heart Failure - Department of Medicine: Division of CardiologyCharleston, South CarolinaResponsible for ensuring adherence to study guidelines, managing the subject recruitment and informed consent process, providing education to patients and their families, and serving as the primary point of contact for study subjects. Participate in the feasibility review process by reviewing protocols and determining the study patient visit flow and provision of center resources to promote protocol compliance and study participant retention.
UNIV - Program Manager I - Clinical Trials, Heart Failure - Department of Medicine: Division of Cardiology Medical University of South CarolinaUNIV - Program Manager I - Clinical Trials, Heart Failure - Department of Medicine: Division of CardiologyCharleston, SCJob Duties: 35% - Supervision and Management of Research Staff: Responsible for the direct supervision of Cardiology Clinical Research staff (program coordinators, research assistants, etc.) that support clinical trials within the Heart Failure program. 35% - Study Management: Responsible for coordinating study visits, performing assessments (6-minute walk, vitals, etc.), and processing lab samples for any assigned Cardiology clinical trial.
NewResearch Program Coordinator University of South CarolinaResearch Program CoordinatorColumbia, SCp>Logo Posting Number RTF00144PO26 USC Market Title Research Program Coordinator Link to USC Market Title https://uscjobs.sc.edu/titles/156413 Business Title (Internal Title) Research Program Coordinator Campus Columbia Work County Richland College/Division Arnold School of Public Health Department ASPH Communication Sciences and Disorders Anticipated Hiring Range Commensurate with experience Location of Vacancy Part/Full Time Full Time Hours per Week 37.5 Work Schedule. The Research Program Coordinator will work closely with the faculty principal investigator, Dr. Jessica Klusek, and grant-funded staff to support and coordinate research on aging in women with fragile X-associated conditions (e.g., fragile X premutation and fragile X syndrome).
NewUNIV - Research Program Coordinator I - Psychiatry: Addiction Sciences Division MUSCUNIV - Research Program Coordinator I - Psychiatry: Addiction Sciences DivisionCharleston, South CarolinaPrior research experience in a lab, knowledge of REDCap data entry, management, reporting tools, interviewing research participants, conducting structured clinical interviews, neuropsychological tests and collecting biospecimens – including drawing blood and MRI assessments not required but valued. Applies technical knowledge to: Organize and coordinate biospecimen shipping and prepare reports for the Program Manager as needed; Support functional and structural MRI sessions and data transfer, troubleshoot issues arising during clinical sessions and scanning, and develop alternative approaches.
UNIV - Research Program Coordinator I - Psychiatry: Addiction Sciences Division Medical University of South CarolinaUNIV - Research Program Coordinator I - Psychiatry: Addiction Sciences DivisionCharleston, South CarolinaPrior research experience in a lab, knowledge of REDCap data entry, management, reporting tools, interviewing research participants, conducting structured clinical interviews, neuropsychological tests and collecting biospecimens – including drawing blood and MRI assessments not required but valued. Applies technical knowledge to: Organize and coordinate biospecimen shipping and prepare reports for the Program Manager as needed; Support functional and structural MRI sessions and data transfer, troubleshoot issues arising during clinical sessions and scanning, and develop alternative approaches.
Research Program Manager University of South CarolinaResearch Program ManagerColumbia, SCLogo Posting Number STA00244PO26 Job Family Research Job Function Research Program Management USC Market Title Research Program Manager Link to USC Market Title https://uscjobs.sc.edu/titles/133775 Job Level M0 - Managerial Business Title (Internal Title) Research Program Manager Campus Columbia Work County Richland College/Division College of Nursing Department CON College of Nursing State Pay Range G11 USC Market Range MRI - $69,913 $87,391 $104,870 Anticipated Hiring Range Salary commensurate with qualifications Location of Vacancy Part/Full Time Full Time Hours per Week 37.5 Work Schedule. The University of South Carolina College of Nursing invites applications for a full-time, on-site Research Program Manager To provide strategic and operational leadership for the Center for Advancing Chronic Care Outcomes through Research and Innovation (ACORN) portfolio of funded and unfunded research activities.
Registered Nurse (RN)- Research, Pediatric 9 Medical Park, FT, Day Prisma HealthRegistered Nurse (RN)- Research, Pediatric 9 Medical Park, FT, DayColumbia, SCProvides 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.
Registered Nurse (RN)- Research, Pediatric Oncology 9 Medical Park , FT, Day Prisma HealthRegistered Nurse (RN)- Research, Pediatric Oncology 9 Medical Park , FT, DayColumbia, SCProvides 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 Specialist State of South CarolinaResearch SpecialistRichland County, SCThe research specialist will work with the faculty principal investigator and grant staff to contribute to a longitudinal NIH -funded research study conducting assessments, managing data, organizing findings and preparing reports. In addition, our Palmetto College campuses in Salkehatchie, Union, Lancaster and Sumter enable students to earn associate or bachelor's degrees through a combination of in-person, online or blended learning.
UNIV - Open Rank Research Faculty - Surgery MUSCUNIV - Open Rank Research Faculty - SurgeryCharleston, South CarolinaThe successful candidate will have a strong track record of extramural funding, play a pivotal role working with PhD investigators and surgeon scientists to advance evidence-based practices, and improve healthcare delivery through the application of health services and outcomes analytic principles. Physical Requirements: (Note: The following descriptions are applicable to this section: Continuous - 6-8 hours per shift; Frequent - 2-6 hours per shift; Infrequent - 0-2 hours per shift) Ability to perform job functions in an upright position.
UNIV - Open Rank Research Faculty - Surgery Medical University of South CarolinaUNIV - Open Rank Research Faculty - SurgeryCharleston, SCThe successful candidate will have a strong track record of extramural funding, play a pivotal role working with PhD investigators and surgeon scientists to advance evidence-based practices, and improve healthcare delivery through the application of health services and outcomes analytic principles. Physical Requirements: (Note: The following descriptions are applicable to this section: Continuous - 6-8 hours per shift; Frequent - 2-6 hours per shift; Infrequent - 0-2 hours per shift) Ability to perform job functions in an upright position.
Nurse Practitioner or Physician Assistant - Psych: Sleep, Mood, Anxiety Research & Treatment (SMART) Medical University of South CarolinaNurse Practitioner or Physician Assistant - Psych: Sleep, Mood, Anxiety Research & Treatment (SMART)Charleston, SCAbility to bend at the waist, kneel, climb stairs, reach in all directions, fully use both hands and legs, possess good finger dexterity, perform repetitive motions with hands/wrists/elbows and shoulders, reach in all directions. APRN License Type/Certification: AGPNP/ANP (Adult Gerontology Primary Care NP or Adult NP): Adult pts (13 years to death), stable chronic disease state management or primary care setting.
Research Scientist- Remote Community Health Center IncResearch Scientist- RemoteSCRemoteThe system delivers primary care to more than 150,000 patients in Connecticut, and extends access to specialty care for more than 2.5 million individuals across the U.S. It is a national accrediting body for organizations training advanced practice providers, and offers accredited education and training for Medical Assistants in multiple states. As an incubator for new ideas in areas including social justice, the environment, and social determinants of health, the MWHS is addressing challenges faced by providers caring for underserved communities, creating innovative and impactful initiatives led by nationally and internationally recognized experts.