Senior Clinical Research Associate ICON PlcSenior Clinical Research AssociateSCRemoteFlexible 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.
NewClinical Research Associate 1 Allen SpoldenClinical Research Associate 1Charleston, South CarolinaConduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, inspection of study files, and related monitoring functions. Initiate studies performing initiation site visits, arrange for shipment of clinical supplies, case report forms, and other necessary materials.
Per Diem Clinical Research Nurse - Home Visits Science 37Per Diem Clinical Research Nurse - Home VisitsCharleston, SC$50–$55 / hourWith interest/expertise in Science 37's decentralized model of care delivery, the Mobile Research Nurse will perform delivery of care to participants as well as collaborate with brick and mortar sites, if indicated, for shared clinical trial implementation. Science 37's Nursing Solutions Group brings together expert nurses who share a passion for organizing, planning and implementing mobile clinical nurse services to participants in clinical trials.
Clinical 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;].
Clinical Trial Liaison / Clinical Research Lead ICON PlcClinical Trial Liaison / Clinical Research LeadSCProactively find opportunities to reach new patients, accelerate enrollment and increase impact at priority sites, including for example, novel site models, community-based research initiatives etc. Act as a key liaison between field teams, vendors, and investigators, ensuring alignment, shared purpose, and continuous knowledge transfer.
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.
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;].
Per Diem Clinical Research Nurse - Home Visits Science 37 IncPer Diem Clinical Research Nurse - Home VisitsCharleston, SC$50–$55 / hourWith interest/expertise in Science 37's decentralized model of care delivery, the Mobile Research Nurse will perform delivery of care to participants as well as collaborate with brick and mortar sites, if indicated, for shared clinical trial implementation. Science 37's Nursing Solutions Group brings together expert nurses who share a passion for organizing, planning and implementing mobile clinical nurse services to participants in clinical trials.
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.
UNIV - Clinical Research Assistant - Department of Medicine: Division of Pulmonary MUSCUNIV - Clinical Research Assistant - 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.
UNIV - Clinical Research Assistant - Department of Medicine: Division of Pulmonary Medical University of South CarolinaUNIV - Clinical Research Assistant - Department of Medicine: Division of PulmonaryCharleston, SCJob Duties: 35% - 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.
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.
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 – 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, 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, 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.
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 - 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.
UNIV - 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.
UNIV - Research Finance Billing Compliance Analyst - Hollings Cancer Center Medical University of South CarolinaUNIV - Research Finance Billing Compliance Analyst - Hollings Cancer CenterCharleston, SCAfter the notification that the study has been pushed to the Universitys 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 Universitys system called SPARCRequest (Services, Pricing, & Application for Research Centers) that outlines the study procedures and proper billing designations per the PRA document.
Research Assistant / Medical Assistant Alcanza Clinical Research LLCResearch Assistant / Medical AssistantNorth Charleston, SCResponsibilities may include but are not limited to: Under the direction of the Site Manager/Director and the Principal/Sub Investigators, assists the CRCs and other site staff in their responsibilities by conducting the following according to study protocol: Assists with the basic screening of patients for study enrollment; Assists with patient follow-up visits; Documents in source clinic charts; Enters data in EDC and answers queries; Obtains vital signs and ECGs; May perform blood draws; 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; Request and track medical record requests; Enters data in EDC and answers queries; Assists the CRC with updating and maintaining logs and filing in charts, and with chart filing; and. Schedules subjects for study visits, conducts appointment reminders, and reschedules visits if needed; Ensures study related reports and patient results are reviewed by the Research Coordinator and/or investigator in a timely manner.
Research Assistant / Medical Assistant Alcanza Clinical ResearchResearch Assistant / Medical AssistantCharleston, South CarolinaResponsibilities may include but are not limited to: Under the direction of the Site Manager/Director and the Principal/Sub Investigators, assists the CRCs and other site staff in their responsibilities by conducting the following according to study protocol: Assists with the basic screening of patients for study enrollment; Assists with patient follow-up visits; Documents in source clinic charts; Enters data in EDC and answers queries; Obtains vital signs and ECGs; May perform blood draws; 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; Request and track medical record requests; Enters data in EDC and answers queries; Assists the CRC with updating and maintaining logs and filing in charts, and with chart filing; and . Schedules subjects for study visits, conducts appointment reminders, and reschedules visits if needed; Ensures study related reports and patient results are reviewed by the Research Coordinator and/or investigator in a timely manner.
UNIV - Research Study Coordinator-Hollings Cancer Center Medical University of South CarolinaUNIV - Research Study Coordinator-Hollings Cancer CenterCharleston, SCSummary: 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.
UNIV - 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 Program Coordinator II – Advanced - Pediatrics: PRG MUSCUNIV - Research Program Coordinator II – Advanced - Pediatrics: PRGCharleston, South Carolina3. Study visit preparation and documentation: Provides oversight and training to study team members, including clinic staff, regarding preparation of study visits, maintenance of subject level documentation and creation of study level SOPs. 2. Gene Therapy Specific Communications: Facilitates gene therapy specific coordination with various departments including but not limited to cryo-preservation, apheresis, radiology, bone marrow transplant team, and fertility banking.
NewUNIV - Research Program Coordinator II - Advanced - Pediatrics: PRG Medical University of South CarolinaUNIV - Research Program Coordinator II - Advanced - Pediatrics: PRGCharleston, SCStudy visit preparation and documentation: Provides oversight and training to study team members, including clinic staff, regarding preparation of study visits, maintenance of subject level documentation and creation of study level SOPs. Gene Therapy Specific Communications: Facilitates gene therapy specific coordination with various departments including but not limited to cryo-preservation, apheresis, radiology, bone marrow transplant team, and fertility banking.
NewUNIV - Research Program Coordinator II – Advanced - Pediatrics: PRG Medical University of South CarolinaUNIV - Research Program Coordinator II – Advanced - Pediatrics: PRGCharleston, South Carolina3. Study visit preparation and documentation: Provides oversight and training to study team members, including clinic staff, regarding preparation of study visits, maintenance of subject level documentation and creation of study level SOPs. 2. Gene Therapy Specific Communications: Facilitates gene therapy specific coordination with various departments including but not limited to cryo-preservation, apheresis, radiology, bone marrow transplant team, and fertility banking.
UNIV - 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.
UNIV - Research Regulatory Specialist - Hollings Cancer Center Medical University of South CarolinaUNIV - Research Regulatory Specialist - Hollings Cancer CenterCharleston, SC$39,764–$56,670 / yearOversees 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.
UNIV - 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.
UNIV - 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.
UNIV - Research Specialist I - Department of Neurosurgery: Pediatric MUSCUNIV - Research Specialist I - Department of Neurosurgery: PediatricCharleston, 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 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.
UNIV - 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.
UNIV - Statistical Research Analyst - Orthopaedic Spine - Department of Orthopaedics MUSCUNIV - Statistical Research Analyst - Orthopaedic Spine - Department of OrthopaedicsCharleston, South CarolinaWhile experiencing the field of orthopaedic surgery hands-on, the analyst will assist our orthoapedic spine physicians in continuing their extensive research being conducting for the field as a whole, while also providing care to their patients- whether in the clinic or the operating room. 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 - TSL Shared Resources Research Specialist - Hollings Cancer Center Medical University of South CarolinaUNIV - 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.
UNIV - Research Specialist I - Department of Dermatology Medical University of South CarolinaUNIV - 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.
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. 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.
UNIV - Research Specialist III - Pharmacology & Immunology Medical University of South CarolinaUNIV - 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.
UNIV - Research Specialist I - Department of Neurosurgery: Pediatric Medical University of South CarolinaUNIV - Research Specialist I - Department of Neurosurgery: PediatricCharleston, 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. 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 - Statistical Research Analyst - Orthopaedic Spine - Department of Orthopaedics Medical University of South CarolinaUNIV - Statistical Research Analyst - Orthopaedic Spine - Department of OrthopaedicsCharleston, SCEntity Medical University of South Carolina MUSC - UnivWorker TypeEmployeeWorker Sub-TypeTemporaryCost CenterCC000989 COM Orthopaedic Surgery & Physical Medicine CCPay Rate TypeHourlyPay GradeUniversity-03Pay Range28060.00 - 39991.00 - 51923.000Scheduled While experiencing the field of orthopaedic surgery hands-on, the analyst will assist our orthopaedic spine physicians in continuing their extensive research and conducting studies for the field as a whole, while also providing care to their patients, whether in the clinic or the operating room.
NewUNIV - Research Program Coordinator I - Psychiatry: ASD Medical University of South CarolinaUNIV - Research Program Coordinator I - Psychiatry: ASDCharleston, SCInitiates 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. 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 Pharmacology & Immunology Medical University of South CarolinaUNIV - Research Specialist I - Department of Pharmacology & ImmunologyCharleston, SCMedical University of South Carolina MUSC - UnivWorker TypeEmployeeWorker Sub-TypeResearch GrantCost CenterCC001034 COM PHARM Operations CCPay Rate TypeHourlyPay GradeUniversity-GEN06Pay Range37200.00 - 48300.00 - 59500.000Scheduled Minimum Requirements A high school diploma and two years work experience in a clinical or research setting a bachelors degree in chemistry biology or other natural life or health care science may be substituted for the two years of required experience.
NewUNIV - Research Program Coordinator I - Psychiatry: ASD MUSCUNIV - Research Program Coordinator I - Psychiatry: ASDCharleston, South CarolinaInitiates 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. 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 III - Department of Pharmacology Medical University of South CarolinaUNIV - Research Specialist III - Department of PharmacologyCharleston, South CarolinaStudies will require data visualization using Python, integration of spatial data sets, graph-based modeling of spatial neighborhood networks, develop machine learning models derived from molecular pathology, and contribute to integrating imaging data with proteomic data. 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.
UNIV – Research Specialist I – Department of Pharmacology & Immunology MUSCUNIV – Research Specialist I – Department of Pharmacology & ImmunologyCharleston, South Carolina$33,339–$47,509 / yearSpecifically, the applicant will utilize cell and molecular biology techniques including but limited to, cell culture, molecular cloning, and enzymatic assays; transfections and gene expression assays; protein, RNA and DNA isolation and separation; ELISA; real-time RTPCR; immunostaining and flow cytometry; proliferation and apoptosis assays and immunohistochemistry. 35% - Perform work involving the use of small laboratory animals, including measuring tumors, collecting fluids and tissues; administering drugs and cells; performing cellular, chemical, and DNA analysis of blood and tissue samples, and freezing and thawing cells.
UNIV - 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.
UNIV - Research Specialist I - Department of Neurosciences Medical University of South CarolinaUNIV - Research Specialist I - Department of NeurosciencesCharleston, SC30% - 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.