MUSCNewNurse Practitioner or Physician Assistant - Neonatology MUSCNurse Practitioner or Physician Assistant - NeonatologyCharleston, SCRequired Minimum Training: Completion of an accredited Physician Assistant program and currently licensed or eligible for licensure as a Physician Assistant or completion of an accredited Nurse Practitioner Program and currently licensed or eligible for licensure as an APRN. Attends intermediate and high risk deliveries independently and performs resuscitation interventions with mastery of physical assessment and technical skills as required – endotracheal intubation, chest compressions, central and peripheral lines, arterial sticks, and medication administration.
The Medicus FirmNewSouth Carolina Psychiatry Leadership Position – Assistant/Associate Program Director The Medicus FirmSouth Carolina Psychiatry Leadership Position – Assistant/Associate Program DirectorFlorence, SCOutdoor Recreation Year-Round- Access to parks, golf courses, and nearby lakes, plus close proximity to South Carolinas coast for weekend getaways. Be part of a nationally recognized academic health system and play a pivotal role in shaping the next generation of psychiatrists while expanding access to behavioral health care across South Carolina.
Midlands Neurology and Pain Associates, P.A.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.
Prisma HealthClinical 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.
MUSCNewUNIV - Research Assistant - Journey - Pediatrics: PRG MUSCUNIV - Research Assistant - Journey - Pediatrics: PRGCharleston, South CarolinaThis includes calling subjects to confirm appointments, filling documents, obtaining signatures from research staff in other MUSC locations, assisting with medical history and adverse event collection and documentation, and reviewing outside medical records. Help study recruitment efforts by completing pre-screening phone calls, reviewing medical charts, and speaking with subjects directly about enrolling studies during clinic visits.
Medical University of South CarolinaUNIV - 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.
Velocity Clinical Research, Inc.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.
MUSCUNIV - 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.
MUSCUNIV - Research Program Assistant: Journey - Pediatrics: PRG MUSCUNIV - Research Program Assistant: Journey - Pediatrics: PRGCharleston, South CarolinaThis includes calling subjects to confirm appointments, filling documents, obtaining signatures from research staff in other MUSC locations, assisting with medical history and adverse event collection and documentation, and reviewing outside medical records. Help study recruitment efforts by completing pre-screening phone calls, reviewing medical charts, and speaking with subjects directly about enrolling studies during clinic visits.
Medical University of South CarolinaUNIV - Research Program Assistant: Journey - Pediatrics: PRG Medical University of South CarolinaUNIV - Research Program Assistant: Journey - Pediatrics: PRGCharleston, SCAbility to perform job functions in an upright position Frequent Ability to perform job functions in a seated position Frequent Ability to perform job functions while walkingmobile Frequent Ability to work indoors Continuous Ability to work outdoors in all weather and temperature extremes Infrequent Ability to work in confinedcramped spaces Infrequent Ability to perform job functions from kneeling positions Infrequent Ability to squat and perform job functions Infrequent Ability to perform pinching operations Infrequent Ability to fully use both handsarms Continuous Ability to perform repetitive motions with handswristselbows and shoulders Frequent Ability to reach in all directions Frequent Possess good finger dexterity Continuous Ability to maintain tactile sensory functions Continuous Ability to lift and carry 15 lbs unassisted Infrequent Ability to lift objects up to 15 lbs from floor level to height of 36 inches unassisted Infrequent Ability to lower objects up to 15 lbs from height of 36 inches to floor level unassisted Infrequent Ability to pushpull objects up to 15 lbs unassisted Infrequent Ability to maintain 2040 vision corrected in one eye or with both eyes Continuous Ability to see and recognize objects close at hand Frequent Ability to see and recognize objects at a distance Frequent Ability to determine distancerelationship between objects depth perception Frequent Good peripheral vision capabilities Continuous Ability to maintain hearing acuity with correction Continuous Ability to hear and or understand whispered conversations at a distance of 3 feet Frequent Ability to perform gross motor functions with frequent fine motor movements Frequent Ability to work in dusty areas. • Provides administrative pre-screening support to study team may maintain logs and data entry related to screening • Schedules participants for study visits • May also assist with the preparation and gathering of study supplies equipment and documents as needed • Conducts visits for minimal risk studies independently • May also perform assessments for minimal risk studies or for greater than minimal risk studies under direct supervision • Collects data directly from participant or from the electronic medical record • Collects prepares ships and or maintains inventory of biological research specimens and processes and ships labs • Conducts and or documents consent for participants in minimal risk studies • May conduct consent for studies greater than minimal risk under direct supervision • Files regulatory documents and reports • Creates a broad array of regulatory submissions initial study applications for minimal risk studies • Creates and submits simple regulatory reports personnel amendments and continuing review applications to the IRB • Prepares for study monitoring and study audit visits • May assist with addressing findings and resolving queries under supervision • Collects prepares or processes adverse events under supervision • Administratively files external SAE reports or IRB SAE reports.
MUSCNurse Practitioner or Physician Assistant - Psych: Sleep, Mood, Anxiety Research & Treatment (SMART) MUSCNurse Practitioner or Physician Assistant - Psych: Sleep, Mood, Anxiety Research & Treatment (SMART)Charleston, South CarolinaAbility 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.
University of South CarolinaResearch Assistant Professor University of South CarolinaResearch Assistant ProfessorColumbia, SCLogo Posting Number: RTF00050PO21 USC Market Title: Research Assistant Professor Link to USC Market Title: [insert link] Business Title: Research Assistant Professor Campus: Columbia Work County: Richland College Division: College of Pharmacy Department: COP Drug Discovery and Biomedical Sciences Location of Vacancy: Part-time. Under limited supervision of the Principal Investigator (PI), the Research Assistant Professor will evaluate research projects for consideration in the Center for Translational Therapeutics (CTT) - Drug Design and Synthesis Core (DDBS) department at the College of Pharmacy and develop synthetic routes and implement synthesis for compounds requested by the DDBS.
Alcanza Clinical ResearchClinical 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;].
Abacus Service CorporationNewAPI Developer & Application Analyst Epic Research Team Abacus Service CorporationAPI Developer & Application Analyst Epic Research TeamColumbia, SCRemoteIn this role, you will focus on building secure data structures, data validation, analyzing large datasets, and web development for data visualization. You will serve as an interface and API Developer and Application Analyst, supporting the integration of third-party systems with the MUSC Epic Electronic Health Record (EHR) system.
NavitasPartnersNewAPI Developer & Application Analyst – Epic Research Team - 0602 NJ #1 NavitasPartnersAPI Developer & Application Analyst – Epic Research Team - 0602 NJ #1Charleston, SCRemoteSeeking an experienced API Developer & Application Analyst to support an Epic Research Team responsible for healthcare data integration, interoperability, and clinical research system connectivity. Develop, implement, and maintain integrations between Epic EHR and third-party research applications.
MUSCUNIV - 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.
Shriners Children'sClinical 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.
Actalent IncClinical Research Coordinator (LOCATED In Atlanta) Actalent IncClinical Research Coordinator (LOCATED In Atlanta)charleston, SC$28–$30 / hourOversee oncology trials and research projectsDevelop research protocols and grant proposalsPerform patient evaluations and administer medicationsTrain and supervise staffEnsure compliance with regulations through auditsManage financial accounts and authorize purchasesDevelop strategies for participant recruitment and retentionInterface with study sponsors and resolve queriesMonitor IRB submissions and respond to requestsQualificationsMUST be able to relocate on your own to the Atlanta, GA area (no relocation offered)MUST have Clinical Research Coordinator (CRC) experience3+ years of solid CRC experience in oncology or interventional drug trials in other therapeutic areasTwo years of college in a scientific, health related, or business administration program AND 3 years of clinical research experienceORHigh School Diploma or GED AND3+ years of clinical research experiencePay and BenefitsThe pay range for this position is $28.00 - $30.00/hr. Clinical Research Coordinator (LOCATED in Atlanta, GA)MUST be able to relocate on your own to the Atlanta, GA area (no relocation offered)Manage and coordinate oncology clinical research trials, including patient recruitment, protocol development, and data management.
MUSCNewUNIV - TSL Shared Resources Research Specialist - Hollings Cancer Center MUSCUNIV - TSL Shared Resources Research Specialist - Hollings Cancer CenterCharleston, South Carolina35%Performs automated nucleic acid extraction, library preparation for different single cell sequencing (10X Genomics) and different RNA next-generation sequencing (NGS), runs droplet digital PCR (ddPCR), and Nanostring GeoMX Digital Spatial Profiler (DSP) on various clinical and non-clinical samples. Promega Maxwell, NGS, single-cell sequencing, NanoString systems, droplet digital PCR, Tapestation, Cellometer, Covaris Ultrasonicator, and Miltenyi tissue dissociator); provides project management for studies involving such platforms, and proactively consults primary scientific literatures when needed.
Occupons QuebecRemote Market Research Assistant Earn Up to $50/Task Occupons QuebecRemote Market Research Assistant Earn Up to $50/TaskRock Hill, SOUTH CAROLINARemoteYou will complete a short screening form so our system can match you with relevant consumer research opportunities within our national insights program. All tasks are conducted online and can be completed outside traditional business hours.
MUSCUniv- Assistant Professor Basic Science Research- Department of Biomedical and Community Health Sciences MUSCUniv- Assistant Professor Basic Science Research- Department of Biomedical and Community Health SciencesCharleston, South CarolinaEdwards College of Dental Medicine seeks a dynamic and innovative Assistant Professor to develop an independent, externally funded research program focused on wound healing, musculoskeletal repair and regeneration, with a complementary emphasis on alveolar bone regeneration and craniofacial biology. The Department seeks a dynamic and innovative Assistant Professor to develop an independent, externally funded research program focused on wound healing, musculoskeletal repair and regeneration, with a complementary emphasis on alveolar bone regeneration and craniofacial biology.
Alcanza Clinical ResearchClinical Research Physician - Internal Medicine - Full time (32-40 hours per week) Alcanza Clinical ResearchClinical Research Physician - Internal Medicine - Full time (32-40 hours per week)Charleston, South CarolinaEssential Job Duties:Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes . The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes.
Alcanza Clinical ResearchClinical Research Physician (part time) - Metabolic: Endocrine, Hepatology, GI Alcanza Clinical ResearchClinical Research Physician (part time) - Metabolic: Endocrine, Hepatology, GICharleston, South CarolinaEssential Job Duties:Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes . The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes.
State of South CarolinaNewResearch 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.
MUSCUNIV - Clinical Assistant Professor - Psychiatry: Sleep, Mood, Anxiety Research & Treatment (SMART) Division MUSCUNIV - Clinical Assistant Professor - Psychiatry: Sleep, Mood, Anxiety Research & Treatment (SMART) DivisionCharleston, South CarolinaThe Sleep, Mood, Anxiety Research & Treatment (SMART) Division within the Department of Psychiatry and Behavioral Sciences at the Medical University of South Carolina (MUSC) in Charleston, SC is seeking a full-time faculty member to provide evidence-based outpatient treatment for a wide spectrum of sleep, anxiety or mood disorders, including common co-morbid sensory processing conditions (tinnitus, eating, smell & taste disturbances). 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.
MUSCNewUNIV - Assistant Director of Community Site Research - Hollings Cancer Center MUSCUNIV - Assistant Director of Community Site Research - Hollings Cancer CenterCharleston, South CarolinaExamples include partnering with the University administrative offices to evaluate opportunities to streamline trial activation workflows; Collaborating with Office of Clinical Research (OCR) to align prospective reimbursement analysis and research billing segregation practices within HCC community sites; Supporting OCR Advarra team for establishing new training and policies for leveraging Advarra tools such as OnCore, eReg, and eConsent; Collaborating with clinical service lines to support high quality and timely data source documentation for clinical evaluations such as RECIST or central imaging and pathology study submission requirements. Monitors NCORP trial accrual and works with the NCORP mPIs to develop initiatives for NCORP affiliates in meeting of exceeding accrual targets Preferred Knowledge skills and abilities: Must be knowledgeable of work guides and procedures and ensure that the monitoring team is accurately reviewing competencies against current policies, work guides and best practices.
MUSCUNIV - Research Finance Billing Compliance Analyst - Hollings Cancer Center MUSCUNIV - Research Finance Billing Compliance Analyst - Hollings Cancer CenterCHARLESTON, South CarolinaAfter the notification that the study has been pushed to the University’s system called SPARCRequest (Services, Pricing, & Application for Research Centers), this role will begin the creation of the important research billing compliance grid that outlines the study procedures and proper billing designations per the PRA documents. After approval confirmation has been received this role will begin the revision of the research billing compliance grid the University’s system called SPARCRequest (Services, Pricing, & Application for Research Centers) that outlines the study procedures and proper billing designations per the PRA document.
MUSCNewUNIV - Research Program Assistant - Journeyman - Department of PHS MUSCUNIV - Research Program Assistant - Journeyman - Department of PHSCharleston, South CarolinaThe Department of Public Health Sciences at The Medical University of South Carolina is seeking a full-time Program Assistant to work on research projects focused on family caregivers of cancer patients. 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.
MUSCUNIV - Research Regulatory Specialist - Hollings Cancer Center MUSCUNIV - Research Regulatory Specialist - Hollings Cancer CenterCHARLESTON, South CarolinaOversees the regulatory activities for federal, corporate, and institutional research projects submitted and activated at the Hollings Cancer Center and promotes high quality and efficient regulatory performance as required by the NCI Core Grant. - Interfaces with relevant MUSC, sponsor, and Clinical Research Organization (CRO) functional leads to ensure appropriate prioritization of essential document creation to facilitate synchronized start-up and ensure task list deadlines are met.
MUSCUNIV - Research Specialist I - Department of Regenerative Medicine MUSCUNIV - Research Specialist I - Department of Regenerative MedicineCharleston, South Carolina$31,561–$44,977 / yearMinimum Requirements: A high school diploma and two years work experience in a clinical or research setting; a bachelor's degree in chemistry, biology, or other natural, life or health care science may be substituted for the two years of required experience. A high school diploma and two years work experience in a clinical or research setting; a bachelor's degree in chemistry, biology, or other natural, life or health care science may be substituted for the two years of required experience.
MUSCUNIV - Research Specialist I - Department of Dermatology MUSCUNIV - Research Specialist I - Department of DermatologyCharleston, South CarolinaThe Research Specialist I will work under general supervision and will support ongoing laboratory research by performing routine molecular, cellular, and histological techniques, assisting with animal studies, and contributing to laboratory organization, safety, and regulatory compliance. Minimum Requirements: A high school diploma and two years work experience in a clinical or research setting; a bachelor's degree in chemistry, biology, or other natural, life or health care science may be substituted for the two years of required experience.
MUSCUNIV - Research Specialist III - Pharmacology & Immunology MUSCUNIV - Research Specialist III - Pharmacology & ImmunologyCharleston, South CarolinaThe selected candidate will be responsible for the maintenance and logistical organization of a basic science laboratory, with particular emphasis on helping the post-docs and staff scientist with breeding of animals and their murine models of leukemia and HCT. Facilitate general maintenance of the research space by working with MUSC to ensure that the laboratory area is maintained and that repairs, waste disposal, and cleaning needs are addressed in a timely manner.
MUSCUNIV - Research Specialist I - Department of Pharmacology & Immunology MUSCUNIV - Research Specialist I - Department of Pharmacology & ImmunologyCharleston, South CarolinaMinimum Requirements: A high school diploma and two years work experience in a clinical or research setting; a bachelor's degree in chemistry, biology, or other natural, life or health care science may be substituted for the two years of required experience. The selected candidate will be responsible for the maintenance and logistical organization of a basic science laboratory, with particular emphasis on performing cell and molecular biology techniques, and ordering and maintaining lab supplies.
MUSCUNIV - Research Specialist III - Department of Pharmacology MUSCUNIV - Research Specialist III - Department of PharmacologyCharleston, South CarolinaThis includes growing human brain endothelial cells on Transwell inserts placed in an EVOM apparatus and measuring a trans endothelial electrical resistance to assure tight junction presence across the monolayer and then adding nanotubes to the apical domain and follow their shuttling to the basolateral domain. Tasks will involve but are not limited to the following: preparing nanotubes of defined length and loading them with small molecule drugs or biologics (monoclonal antibodies) for use in in vitro blood-brain barrier (BBB) transit studies, and for BBB transit studies in mice.
MUSCUNIV - Research Specialist I - Department of Biochemistry MUSCUNIV - Research Specialist I - Department of BiochemistryCharleston, South CarolinaMinimum Requirements: A high school diploma and two years work experience in a clinical or research setting; a bachelor's degree in chemistry, biology, or other natural, life or health care science may be substituted for the two years of required experience. The Department of Biochemistry & Molecular Biology at the Medical University of South Carolina (MUSC) invites applications for a Research Specialist I position in the laboratory of Dr. Zhang, who joined MUSC in November 2025.
MUSCUNIV - Research Specialist III - Pharmacology and Immunology MUSCUNIV - Research Specialist III - Pharmacology and ImmunologyCharleston, South CarolinaOngoing projects involve investigating acute and chronic neuroimmune responses occurring after stroke or after different types of traumatic brain injury, including the long-term neurodegenerative sequalae of injury. Minimum Requirements: A bachelor's degree in chemistry, biology, or other natural, life or health care science directly related to the assigned area of research and two years advanced journel-level work experience in a clinical or research setting.
Medical University of South CarolinaUNIV - Research Specialist I - Department of Biochemistry Medical University of South CarolinaUNIV - Research Specialist I - Department of BiochemistryCharleston, SCMinimum Requirements: A high school diploma and two years work experience in a clinical or research setting; a bachelor's degree in chemistry, biology, or other natural, life or health care science may be substituted for the two years of required experience. Job Purpose: The Department of Biochemistry & Molecular Biology at the Medical University of South Carolina (MUSC) invites applications for a Research Specialist I position in the laboratory of Dr. Zhang, who joined MUSC in November 2025.
Medical University of South CarolinaUNIV - Research Specialist I - Department of Pharmacology & Immunology Medical University of South CarolinaUNIV - Research Specialist I - Department of Pharmacology & ImmunologyCharleston, SC$37,200–$48,300 / yearEntity & Compensation Details Entity: Medical University of South Carolina (MUSC) Worker Type: Employee Worker Sub-Type: Research Grant Cost Center: CC001034 COM PHARM Operations CCP Pay Rate Type: Hourly Pay Grade: University-GEN06 Pay Range: $37,200.00 - $48,300.00 - $59,500.00 Scheduled Weekly Hours: 40 Work Shift: Not specified Position Start Date: May 1 - September 1, 2026 ## Job Description This Research Specialist I position will provide technical assistance to the Principal Investigator on cancer research studies and assist with lab operations. Facilitate general maintenance of the research space by working with MUSC to ensure that the laboratory area is maintained and that repairs, waste disposal, and cleaning needs are addressed in a timely manner.
MUSCUNIV - Pediatric Oncology and Cellular Therapy Faculty - Pediatrics: Darby Children's Research Institute MUSCUNIV - Pediatric Oncology and Cellular Therapy Faculty - Pediatrics: Darby Children's Research InstituteCharleston, South CarolinaThe Medical University of South Carolina is strongly supported by an NCI designated Hollings Cancer Center, a top ranked Department of Pediatrics whose ranking keeps climbing, and new MUSC Shawn Jenkins Children’s Hospital, and a Cellular Therapy Program designated as over-performing by the Center for International Blood and Marrow Transplant Research, which together provide outstanding childhood cancer care. This position is a joint recruiting effort between the Division of Pediatric Hematology and Oncology in the Department of Pediatrics, the Darby Children’s Research Institute, the Hollings Cancer Center, and the Integrated Center for Cellular Therapy at the Medical University of South Carolina (MUSC) in Charleston, South Carolina.
MUSCUNIV - Research Program Coordinator I - Psychiatry: Addiction Sciences Division MUSCUNIV - Research Program Coordinator I - Psychiatry: Addiction Sciences DivisionCharleston, South CarolinaThe candidate will assist the Principal Investigator in the recruitment of research participants, the collection of psychological research data, data entry and organizational tasks for studies being conducted in the Department of Psychiatry/Addiction Sciences Division. Initiates and maintains accurate and comprehensive documentation as required by the FDA, DOD, Institutional Review Board, study sponsors, and Good Practice Guidelines in connection with research trials.
DP ProfessionalsAV Technology Research Analyst DP ProfessionalsAV Technology Research AnalystColumbia, SCRequired education/equivalencies: Bachelor’s degree in Computer Science, Information Technology, or other job-related degree; OR, Associates degree in CS, IT, or other job-related degree plus 2 years of work-related experience; OR, 4 years job-related work experience (total 6 years without a degree) . Minimum required work experience: 2 years of specific knowledge of the technologies or products to be supported, including 1 year of experience directly supporting the technologies or products.
MUSCUNIV - Senior Research Associate - Data Manager - ECHO - Department of PHS MUSCUNIV - Senior Research Associate - Data Manager - ECHO - Department of PHSCharleston, South Carolina25% - Utilize data management system to maintain participant records, track recruitment progress and study milestones, and generate recruitment and study visit reports for PI and the study team of the ECHO program at MUSC. 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.
Medical University of South CarolinaUNIV - Senior Research Associate - Data Manager - ECHO - Department of PHS Medical University of South CarolinaUNIV - Senior Research Associate - Data Manager - ECHO - Department of PHSCharleston, SC25 - Utilize data management system to maintain participant records track recruitment progress and study milestones and generate recruitment and study visit reports for PI and the study team of the ECHO program at MUSC. The position will be responsible for database management ensuring data quality and regulatory compliance overseeing medical record abstraction and developing efficient data workflows to support research and reporting.
MUSCUNIV - Research Specialist III - Department of Regenerative Medicine MUSCUNIV - Research Specialist III - Department of Regenerative MedicineCharleston, South Carolina$45,530–$64,885 / yearPerform simple to complex laboratory procedures in one or more areas of laboratory investigation such as: an isolation of primary cells from human and mouse tissues; phenotypic and functional characterization of immune responses by high dimension flow and mass cytometry; in vivo experiments using models of colon cancer, inflammatory bowel disease, etc. The individual will be under the supervision of the PI, will participate in routine experiments and the maintenance of a basic biomedical science laboratory, develop protocols, perform complex molecular biology and cell biology assays, manage budget and ordering.
MUSCUNIV - Research Program Assistant I - Psychiatry: Addiction Sciences Division MUSCUNIV - Research Program Assistant I - Psychiatry: Addiction Sciences DivisionCharleston, South CarolinaPhysical 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. Prepare tracking reports as needed and present status to the research team monthly, including areas of improvement regarding recruitment procedures.
MUSCUNIV - Research Specialist I - Department of Neurosciences MUSCUNIV - Research Specialist I - Department of NeurosciencesCharleston, South Carolina30% - Perform various experimental procedures including, but not limited to, executing behavioral protocols (testing mice on cognitive tasks) and alcohol self-administration studies, administering drugs by various routes of administration (injection, inhalation, infusion), preparing drugs and solutions, conducting stereotaxic surgery to implant chronic indwelling cannula in mice for long-term recordings or behavioral manipulations, facilitate data collection for fiber photometry and in vivo electrophysiology studies from mice during tasking measuring cognition, alcohol drinking, and anxiety-like behaviors. 20% - Administrative duties include lab organization and cleaning of working benchtops, supply ordering, animal ordering and inventory, coordinate and manage the behavioral testing rooms and animal breeding colony, maintain and schedule service for laboratory equipment, and perform daily animal husbandry activities to maintain the health of animals in support of the research program and according to regulatory policies.
MUSCDeputy CIO, Academic and Research Technology - Information Solutions MUSCDeputy CIO, Academic and Research Technology - Information SolutionsCHARLESTON, South CarolinaEstablish integration strategies and oversee specialty academic systems across the portfolio, including Learning Management Systems, clinical education and GME platforms, curriculum management, simulation, testing and assessment, library systems, and faculty credentialing, in partnership the Office of Enrollment Management (which includes Registrar, Financial Aid, Admissions, and Data & Reporting), Academic Affairs, and Student Services offices to meet institutional, accreditor, and regulatory expectations. Lead development and governance of research data infrastructure (research data warehouses, biorepository systems, REDCap, clinical trial management platforms) and advance research computing capabilities, including high-performance computing, cloud research environments, and secure data enclaves in partnership with the Office of Research and Sponsored Programs, IRB, and research compliance, meeting federal grant and data security requirements.
MUSCUNIV - Research Specialist I - Department of Medicine: Division of Rheumatology MUSCUNIV - Research Specialist I - Department of Medicine: Division of RheumatologyCharleston, South CarolinaExperience working with research databases, laboratory information management systems (LIMS), or data management platforms (e.g., REDCap, Freezerworks, PowerBI, Excel or similar systems). 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.
University of South CarolinaResearch Coordinator University of South CarolinaResearch Coordinatorcolumbia, SCLogo Posting Number TMP02499PO25 Job Code Title Research Coordinator Advertised Title Research Coordinator Campus Columbia College/Division Arnold School of Public Health Department ASPH Health Services Policy and Management Salary $64,000 Location of Vacancy Part/Full Time Full Time Hours per Week 40 Work Schedule. 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.
University of South CarolinaResearch Scientist University of South CarolinaResearch ScientistColumbia, SCThe Department of Chemistry and Biochemistry seeks to hire a Post-Doctoral Fellow to develop microbial heterologous expression systems via synthetic biology technologies, aiming to utilize the vast genetic potentials of the biosynthetic gene clusters from cultivatable microbes for production of bioactive natural products, such as antibiotics and anticancer agents. Job Duty: Develop microbial heterologous expression systems via synthetic biology technologies aiming to utilize the vast genetic potentials of the biosynthetic gene clusters from cultivatable microbes for production of bioactive natural products.