Assistant Electrical Supervisor – 2nd Shift MUSCAssistant Electrical Supervisor – 2nd ShiftCharleston, South CarolinaUnder limited supervision, the Assistant Electrical Supervisor assists in the management, supervision and administration of the MUSC Enterprise, MUHA and University Facilities Electrical Systems MUSC Enterprise MUHA and University staff electricians. This position is knowledgeable with the Hospital Building, Research, Automation and Fire Alarm Systems and assists in managing all utility outages for the MUSC Enterprise, Hospital and University Facilities.
Assistant Electrical Supervisor - 2nd Shift Medical University of South CarolinaAssistant Electrical Supervisor - 2nd ShiftCharleston, SCUnder limited supervision, the Assistant Electrical Supervisor assists in the management, supervision and administration of the MUSC Enterprise, MUHA and University Facilities Electrical Systems MUSC Enterprise MUHA and University staff electricians. This position is knowledgeable with the Hospital Building, Research, Automation and Fire Alarm Systems and assists in managing all utility outages for the MUSC Enterprise, Hospital and University Facilities.
NewAssistant Electrical Supervisor – 2nd Shift Medical University of South CarolinaAssistant Electrical Supervisor – 2nd ShiftCharleston, South CarolinaUnder limited supervision, the Assistant Electrical Supervisor assists in the management, supervision and administration of the MUSC Enterprise, MUHA and University Facilities Electrical Systems MUSC Enterprise MUHA and University staff electricians. This position is knowledgeable with the Hospital Building, Research, Automation and Fire Alarm Systems and assists in managing all utility outages for the MUSC Enterprise, Hospital and University Facilities.
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, SC30% - Supports the MUSC OCR industry sponsor invoicing program for clinical research; provides and supports Sponsor Invoicing, billing reconciliation, communication and reporting to ensure that earned revenue is realized to support the activities of industry sponsored research: Monitor study startup, invoiceable, milestone, per patient visit and administrative (PRA, OCR Finance, IRB, and CTMS fees) activity to ensure proper and full financial reimbursement for these activities. 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 and provide training, mentorship and guidance for sponsor invoicing within MUSC's Clinical Trial Management System.
UNIV - Clinical Research Assistant - Surgery: Clinical Trials MUSCUNIV - Clinical Research Assistant - Surgery: Clinical TrialsCharleston, South Carolina$37,200–$48,300 / yearNote: 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. This person will also conduct all research in adherence with the FDA Code of Federal Regulations, "Good Clinical Practices”, and adhere to the MUSC IRB regulations for the protection of human subjects.
UNIV - Clinical Research Assistant - Surgery: Clinical Trials Medical University of South CarolinaUNIV - Clinical Research Assistant - Surgery: Clinical TrialsCharleston, South CarolinaNote: 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. This person will also conduct all research in adherence with the FDA Code of Federal Regulations, "Good Clinical Practices”, and adhere to the MUSC IRB regulations for the protection of human subjects.
NewUNIV - Clinical Research Assistant - Department of Medicine: Division of Pulmonary MUSCUNIV - Clinical Research Assistant - Department of Medicine: Division of PulmonaryCharleston, South Carolina25% - Assists research coordinators and management with subject-related activities as needed including: escorting research patients around campus, conducting minor visits (non-interventional trials), transporting research supplies to the ICUs and other inpatient units, performing clinical assessments such as EKG, PFT, 6MWT, vitals monitoring, data entry, and other research procedures as dictated by the protocol; processing, storing, and shipping laboratory specimens within acceptable guidelines; completing subject reminder phone calls; rescheduling subject appointments as necessary; retrieving external medical records; completing initial medical history review of subjects; managing shipments of study related items to and from subjects and CRO/sponsors. 25% - Responsible for meticulous and careful pharmacy and laboratory management for clinical trials, including, but not limited to: receiving study drug and/or device shipments; managing IVRS/IWRS/IXRS forms; documenting receipt, dispensation, return, destruction and quarantine of investigational product/devices when applicable in pharmacy binder; monitoring temperature control; acting as the Investigational Drug Services (IDS) liaison for the Pulmonary & Critical Care and COVID-19 Clinical Research Program; providing education on the pharmacy process to the research team; meeting and reviewing pharmacy documentation with the research monitors.
NewUNIV - Clinical Research Assistant - Department of Medicine: Division of Pulmonary Medical University of South CarolinaUNIV - Clinical Research Assistant - Department of Medicine: Division of PulmonaryCharleston, South Carolina25% - Assists research coordinators and management with subject-related activities as needed including: escorting research patients around campus, conducting minor visits (non-interventional trials), transporting research supplies to the ICUs and other inpatient units, performing clinical assessments such as EKG, PFT, 6MWT, vitals monitoring, data entry, and other research procedures as dictated by the protocol; processing, storing, and shipping laboratory specimens within acceptable guidelines; completing subject reminder phone calls; rescheduling subject appointments as necessary; retrieving external medical records; completing initial medical history review of subjects; managing shipments of study related items to and from subjects and CRO/sponsors. 25% - Responsible for meticulous and careful pharmacy and laboratory management for clinical trials, including, but not limited to: receiving study drug and/or device shipments; managing IVRS/IWRS/IXRS forms; documenting receipt, dispensation, return, destruction and quarantine of investigational product/devices when applicable in pharmacy binder; monitoring temperature control; acting as the Investigational Drug Services (IDS) liaison for the Pulmonary & Critical Care and COVID-19 Clinical Research Program; providing education on the pharmacy process to the research team; meeting and reviewing pharmacy documentation with the research monitors.
NewUNIV - Clinical Research Assistant (Regulatory) - Department of Medicine: Division of Pulmonary MUSCUNIV - Clinical Research Assistant (Regulatory) - Department of Medicine: Division of PulmonaryCharleston, South Carolina35% - Responsible for meticulous and careful management of regulatory documentation of the Program’s regulatory files; maintains up-to-date files of CVs, medical licensure, note-to-files, conflict of interests, training documentation, laboratory certifications and other documents as needed. Will be responsible for preparing regulatory files for on-site monitoring visits, sponsor audits and regulatory authority audits, as well as reconciling and resolving action items following said on-site visits.
NewUNIV - Clinical Research Assistant (Regulatory) - Department of Medicine: Division of Pulmonary Medical University of South CarolinaUNIV - Clinical Research Assistant (Regulatory) - Department of Medicine: Division of PulmonaryCharleston, South Carolina35% - Responsible for meticulous and careful management of regulatory documentation of the Program’s regulatory files; maintains up-to-date files of CVs, medical licensure, note-to-files, conflict of interests, training documentation, laboratory certifications and other documents as needed. Will be responsible for preparing regulatory files for on-site monitoring visits, sponsor audits and regulatory authority audits, as well as reconciling and resolving action items following said on-site visits.
NewUNIV - Research Program Assistant - Surgery: Clinical Trials MUSCUNIV - Research Program Assistant - Surgery: Clinical TrialsCharleston, South Carolina$37,944–$49,266 / yearNote: 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. This person will also conduct all research in adherence with the FDA Code of Federal Regulations, "Good Clinical Practices”, and adhere to the MUSC IRB regulations for the protection of human subjects.
NewClinical Research Coordinator Alcanza Clinical Research LLCClinical Research CoordinatorNorth Charleston, SCScheduling 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;].
UNIV - Research Program Assistant - Advance - Department of Dermatology Medical University of South CarolinaUNIV - Research Program Assistant - Advance - Department of DermatologyCharleston, South CarolinaThis position assists investigators and research staff with participant recruitment, scheduling, data management, regulatory documentation, and study coordination activities while ensuring compliance with institutional, sponsor, IRB, and federal requirements. 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 - Research Program Assistant - Advance - Department of Dermatology MUSCUNIV - Research Program Assistant - Advance - Department of DermatologyCharleston, South CarolinaThis position assists investigators and research staff with participant recruitment, scheduling, data management, regulatory documentation, and study coordination activities while ensuring compliance with institutional, sponsor, IRB, and federal requirements. 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.
NewClinical Research Coordinator DelRicht ResearchClinical Research CoordinatorMount Pleasant, SC$50,000–$55,000 / yearNice-to-have experience includes: Exposure to healthcare, patient care, or clinical trials (nurse, medical assistant, or medical scribe experience is ideal!); comfort with clinical documentation and charting; experience with blood draws, ECGs, and vital signs. Overall, the Clinical Research Coordinator is responsible for delivering an excellent patient experience while driving accurate, efficient study execution, ensuring: Patients have a positive, professional, and comfortable experience throughout their time in our clinic.
UNIV - Research Program Coordinator II - Regulatory Coordinator - Department of Neurology Medical University of South CarolinaUNIV - Research Program Coordinator II - Regulatory Coordinator - Department of NeurologyCharleston, South CarolinaThe Regulatory Coordinator manages study start-up submissions and approvals, facilitates communication with the Institutional Review Board (IRB) and other oversight committees, maintains regulatory compliance throughout the research lifecycle, and serves as a departmental resource to research personnel regarding regulatory requirements, policies, and best practices. This position supports compliance with institutional, state, federal, sponsor, FDA, OHRP, HIPAA, and ICH-GCP requirements to help ensure protection of research participants and successful execution of the department's clinical research portfolio.
UNIV - Research Program Coordinator II - Regulatory Coordinator - Department of Neurology MUSCUNIV - Research Program Coordinator II - Regulatory Coordinator - Department of NeurologyCharleston, South CarolinaThe Regulatory Coordinator manages study start-up submissions and approvals, facilitates communication with the Institutional Review Board (IRB) and other oversight committees, maintains regulatory compliance throughout the research lifecycle, and serves as a departmental resource to research personnel regarding regulatory requirements, policies, and best practices. This position supports compliance with institutional, state, federal, sponsor, FDA, OHRP, HIPAA, and ICH-GCP requirements to help ensure protection of research participants and successful execution of the department's clinical research portfolio.
UNIV - 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. 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 - Research Specialist I - Department of Biochemistry Medical University of South CarolinaUNIV - 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. 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 - Research Program Assistant - Psychiatry: Neuromodulation & Behavioral Medicine Medical University of South CarolinaUNIV - Research Program Assistant - Psychiatry: Neuromodulation & Behavioral MedicineCharleston, South CarolinaDescription of Position: The program assistant will oversee, coordinate, and assist in the screening, recruitment, and enrollment of research participants for clinical treatment trials using behavioral and medication-based interventions for patients with obesity and tobacco use. The program assistant will oversee, coordinate, and assist in the screening, recruitment, and enrollment of research participants for clinical treatment trials using behavioral and medication-based interventions for patients with obesity and tobacco use.