UNIV - Program Manager I - Department of Medicine: Division of Hospital Medicine & Nephrology Medical University of South CarolinaUNIV - Program Manager I - Department of Medicine: Division of Hospital Medicine & NephrologyCharleston, South CarolinaOversee and monitor contract(s) to ensure payments, renewals, extensions or terminations are processed timely initially to include the following: Dialysis Centers, Inc Medical Director Contracts at Nexton, West Ashley, Goose Creek, Mt Pleasant (East Cooper), James Island, Port Royal, Archdale, Home Dialysis. Coordinates the business management functions of programs, grants and contracts and unrestricted funds by reporting directly to the Division Administrator’s for the Hospital Medicine Division and the Nephrology Division and has a matrix reporting relationship with the Departmental Finance and Research Administrator.
UNIV - Program Manager I - Department of Medicine: Division of Hospital Medicine & Nephrology MUSCUNIV - Program Manager I - Department of Medicine: Division of Hospital Medicine & NephrologyCharleston, South CarolinaOversee and monitor contract(s) to ensure payments, renewals, extensions or terminations are processed timely initially to include the following: Dialysis Centers, Inc Medical Director Contracts at Nexton, West Ashley, Goose Creek, Mt Pleasant (East Cooper), James Island, Port Royal, Archdale, Home Dialysis. Coordinates the business management functions of programs, grants and contracts and unrestricted funds by reporting directly to the Division Administrator’s for the Hospital Medicine Division and the Nephrology Division and has a matrix reporting relationship with the Departmental Finance and Research Administrator.
NewHealthcare Data Entry Coordinator - Onsite in Charleston, SC Alcanza Clinical ResearchHealthcare Data Entry Coordinator - Onsite in Charleston, SCCharleston, South CarolinaRequired Skills: Proficiency with computer applications such as Microsoft applications, email, and web applications, and the ability to type proficiently (40+ wpm); Strong organizational skills and attention to detail. Essential Job Duties: In collaboration with other members of the clinical research site teamwork to ensure the entry of clinical visit data in EDC and other clinical data software/systems.
NewHealthcare Data Entry Coordinator Alcanza Clinical Research LLCHealthcare Data Entry CoordinatorNorth Charleston, SCRequired Skills: Proficiency with computer applications such as Microsoft applications, email, and web applications, and the ability to type proficiently (40+ wpm); Strong organizational skills and attention to detail. Essential Job Duties: In collaboration with other members of the clinical research site teamwork to ensure the entry of clinical visit data in EDC and other clinical data software/systems.
UNIV - Research Program Coordinator I - Journey - Department of PHS Medical University of South CarolinaUNIV - Research Program Coordinator I - Journey - Department of PHSCharleston, SCJob Description: Under the direct supervision of the Vice Chair for Research, Program Director and Program Coordinator II (PCII), the Program Coordinator I (PCI) will assist research investigators in the initiation, coordination, and management of clinical research trials and thus has a significant contribution to ensure assurance of sustainability, efficiency, and compliance. Under the direct supervision of the Vice Chair for Research, Program Director and Program Coordinator II (PCII), the Program Coordinator I (PCI) will assist research investigators in the initiation, coordination, and management of clinical research trials and thus has a significant contribution to ensure assurance of sustainability, efficiency, and compliance.
UNIV - Research Program Coordinator I - Journey - Department of PHS MUSCUNIV - Research Program Coordinator I - Journey - Department of PHSCharleston, South CarolinaUnder the direct supervision of the Vice Chair for Research, Program Director and Program Coordinator II (PCII), the Program Coordinator I (PCI) will assist research investigators in the initiation, coordination, and management of clinical research trials and thus has a significant contribution to ensure assurance of sustainability, efficiency, and compliance. Ethics and Participant Safety 10% Under direction provides data for external monitoring reports and/or facilitates completion of documents related to Research Data Security Plans, Data Safety and Monitoring Plans, and Conflict of Interest.
UNIV - Research Specialist I - Department of Regenerative Medicine Medical University of South CarolinaUNIV - Research Specialist I - Department of Regenerative MedicineCharleston, SCMUSC Minimum Training and Experience 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. 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.
UNIV - Research Specialist I - Department of Regenerative Medicine MUSCUNIV - Research Specialist I - Department of Regenerative MedicineCharleston, 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. 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.
EMT - Weekday evenings (Between 7pm-7am) and weekend shifts needed - PRN Alcanza Clinical Research LLCEMT - Weekday evenings (Between 7pm-7am) and weekend shifts needed - PRNNorth Charleston, SCThis position provides support to the Clinical Research Coordinators (CRCs), Site Manager, Principal and Sub Investigators, and other site staff in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs. Essential Job Duties: In collaboration with other members of the clinical research site team, assists with the execution of assigned studies, and support functions as needed.
UNIV - Lab Technologist II - Department of SCTR Medical University of South CarolinaUNIV - Lab Technologist II - Department of SCTRCharleston, South CarolinaUnder direct/general supervision of the Laboratory Technologist III and/or Research Laboratory Manager, the Laboratory Technologist II performs complex laboratory tests and molecular laboratory procedures to support SCTR Research Nexus approved clinical trials. 35% - Support SCTR Research Nexus Laboratory clinical research by performing sample processing, testing, and shipping according to clinical trial documents and with a high level of customer service.
UNIV - Lab Technologist II - Department of SCTR MUSCUNIV - Lab Technologist II - Department of SCTRCharleston, South CarolinaUnder direct/general supervision of the Laboratory Technologist III and/or Research Laboratory Manager, the Laboratory Technologist II performs complex laboratory tests and molecular laboratory procedures to support SCTR Research Nexus approved clinical trials. 35% - Support SCTR Research Nexus Laboratory clinical research by performing sample processing, testing, and shipping according to clinical trial documents and with a high level of customer service.
UNIV - Regulatory Coordinator - Department of Medicine: Division of Pulmonary Medical University of South CarolinaUNIV - Regulatory Coordinator - Department of Medicine: Division of PulmonaryCharleston, SCMaintains accurate study registration as applicable (ClinicalTrials.gov, etc) for all investigator-initiated projects; provides guidance on issues such as when to re-consent subjects, when to report events per IRB policy. This includes coding and building of source structure, field editing based on protocol amendments or usage needs, creating reports and alerts as needed, and alerting study team of any changes made.
UNIV - Regulatory Coordinator - Department of Medicine: Division of Pulmonary MUSCUNIV - Regulatory Coordinator - Department of Medicine: Division of PulmonaryCharleston, South CarolinaMaintains accurate study registration as applicable (ClinicalTrials.gov, etc) for all investigator-initiated projects; provides guidance on issues such as when to re-consent subjects, when to report events per IRB policy. This includes coding and building of source structure, field editing based on protocol amendments or usage needs, creating reports and alerts as needed, and alerting study team of any changes made.
EMT/Paramedic - Weekday evenings (Between 7pm-7am) and weekend shifts needed - PRN Alcanza Clinical ResearchEMT/Paramedic - Weekday evenings (Between 7pm-7am) and weekend shifts needed - PRNCharleston, South CarolinaThis position provides support to the Clinical Research Coordinators (CRCs), Site Manager, Principal and Sub Investigators, and other site staff in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs. Essential Job Duties: In collaboration with other members of the clinical research site team, assists with the execution of assigned studies, and support functions as needed.
Medical Assistant - Weekday evenings (Between 7pm-7am) and weekend shifts needed - PRN Alcanza Clinical ResearchMedical Assistant - Weekday evenings (Between 7pm-7am) and weekend shifts needed - PRNNorth Charleston, South CarolinaThis position provides support to the Clinical Research Coordinators (CRCs), Site Manager, Principal and Sub Investigators, and other site staff in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs. Essential Job Duties: In collaboration with other members of the clinical research site team, assists with the execution of assigned studies, and support functions as needed.
UNIV-Quality Assurance Auditor - Hollings Cancer Center Medical University of South CarolinaUNIV-Quality Assurance Auditor - Hollings Cancer CenterCharleston, South CarolinaThe auditor prepares for NCI National Clinical Trials Network (NCTN) audits, MUSC compliance checks, and sponsor quality control visits by reviewing informed consent documentation, eligibility, treatment administration, adverse events, disease response, and overall data quality. Responsibilities include reviewing research chart organization, patient registration workflows, and documentation practices across systems such as Medidata Rave, TRIAD, electronic patient‑reported outcome platforms, and NCI specimen tracking systems.
APP Lead - Neurosurgery ICU Medical University of South CarolinaAPP Lead - Neurosurgery ICUCharleston, 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. Nurse Practitioner 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.
Nurse Practitioner or Physician Assistant - Burn Surgery Medical University of South CarolinaNurse Practitioner or Physician Assistant - Burn SurgeryCharleston, SCProvides timely, courteous, and efficacious care to patient; examine, diagnose, prescribe treatments and medications, performs or orders tests and/or procedures for a variety of diseases and injuries using applicable medical instruments and equipment within the healthcare delivery system, referring to medical specialist for consultation and communicating with patients' primary physicians as indicated. The Clinical Thermal Injury Specialist Advanced Practiced Provider (APP) provides patient centered healthcare utilizing a holistic and multidisciplinary approach to deliver state of the art care to patients with thermal injury and other skin and soft tissue disorders.
APP Lead - Neurosurgery ICU MUSCAPP Lead - Neurosurgery ICUCharleston, 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. The APP Lead (Nurse Practitioner or Physician Assistant) will provide guidance and oversight to a defined team of APPs working in the NSICU areas, while also working clinically as an APP on the unit.
UNIV-Quality Assurance Auditor - Hollings Cancer Center MUSCUNIV-Quality Assurance Auditor - Hollings Cancer CenterCharleston, South CarolinaThe auditor prepares for NCI National Clinical Trials Network (NCTN) audits, MUSC compliance checks, and sponsor quality control visits by reviewing informed consent documentation, eligibility, treatment administration, adverse events, disease response, and overall data quality. Responsibilities include reviewing research chart organization, patient registration workflows, and documentation practices across systems such as Medidata Rave, TRIAD, electronic patient‑reported outcome platforms, and NCI specimen tracking systems.