190 Results for

Clinical Research Jobs in Charleston, SC

Jobs

Mount Pleasant, SC30+ days ago

Remote

Flexible 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.

Charleston, SC30+ days ago

$52,100–$70,300 Per Year

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 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.

Mt. Pleasant, SC10 days ago

Proactively 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.

North Charleston, SC30+ days ago

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 answering queries • Obtaining vital signs and ECGs • May perform basic lab procedures per protocol such as blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens, and notification of courier for specimen pick-up • Requesting and tracking medical record requests • Updating and maintaining logs, chart filings • Maintaining & ordering study specific supplies • Scheduling subjects for study visits and conducts appointment reminders • Building, updating source as needed • Conducting monitoring visits and resolves issues as needed in a timely manner • Ensuring study related reports and patient results are reviewed by investigator in a timely manner • Filing SAE • Deviation reports to Sponsor and IRB as needed • Documenting and reporting adverse events • Reporting non-compliance to appropriate staff in timely manner • Maintaining positive and effective communication with clients and team members • Always practicing ALCOAC principles with all documentation • May assist with study recruitment, patient enrollment, and tracking as needed • Maintaining confidentiality of patients, customers, and company information • Performing all other duties as requested or assigned • Complete all needed activities for study start-up including completing required training, uploading printing certificates to file in ISF, etc. A Medical Assistant diploma, LPN, VN, EMT credential, or Associates degree AND a minimum of 1 year of clinical research or clinical experience OR an equivalent combination of education and experience is required.

Charleston, SC14 days ago

$50–$55 Per Hour

With 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.

North Charleston, SC10 days ago

Oversee 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.

Charleston, South Carolina30+ days ago

Scheduling subjects for study visits and conducts appointment reminders; Building/updating source as needed; Conducting monitoring visits and resolves issues as needed in a timely manner; Ensuring study related reports and patient results are reviewed by investigator in a timely manner; Filing SAE/Deviation reports to Sponsor and IRB as needed; Documenting and reporting adverse events; Reporting non-compliance to appropriate staff in timely manner; Maintaining positive and effective communication with clients and team members; Always practicing ALCOAC principles with all documentation; May assist with study recruitment, patient enrollment, and tracking as needed; Maintaining confidentiality of patients, customers and company information, 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;].

Charleston, South Carolina11 days ago

Charleston, SC30+ days ago

$50–$55 Per Hour

New!

Charleston, South Carolina4 days ago

Responsibilities 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.

North Charleston, SC30+ days ago

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. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine.

North Charleston, SC30+ days ago

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. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine neurology dermatology psychiatry and general medicine.

Charleston, South Carolina30+ days ago

Essential 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.

Charleston, South Carolina30+ days ago

$37,200–$48,300 Per Year

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. The Research Grant & Regulatory Coordinator provides comprehensive administrative support for clinical and translational research activities.

Charleston, SC30+ days ago

$37,200–$48,300 Per Year

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. The Research Grant & Regulatory Coordinator provides comprehensive administrative support for clinical and translational research activities.

Charleston, SC30+ days ago

Ability 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.

Charleston, SC11 days ago

The 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.

Charleston, South Carolina11 days ago

Charleston, South Carolina30+ days ago

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. 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.

Charleston, South Carolina30+ days ago

Charleston, SC30+ days ago

Job 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.

Charleston, SC30+ days ago

Job 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.

Charleston, South Carolina30+ days ago

CHARLESTON, South Carolina30+ days ago

After 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.

Charleston, SC30+ days ago

After 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.

Charleston, SC17 days ago

This 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.

Charleston, South Carolina17 days ago

Charleston, SC30+ days ago

Ability 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.

Charleston, SC30+ days ago

$39,764–$56,670 Per Year

Oversees 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.

Charleston, South Carolina30+ days ago

The 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.

Charleston, South Carolina7 days ago

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. 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.

Charleston, South Carolina7 days ago

While 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.

Charleston, SC30+ days ago

MUSC Minimum Training and Experience 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. The 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.

Charleston, SC30+ days ago

Medical University of South Carolina MUSC - UnivWorker TypeEmployeeWorker Sub-TypeResearch GrantCost CenterCC000961 COM Dermatology CCPay Rate TypeHourlyPay GradeUniversity-04Pay Range33339.00 - 47509.00 - 61680.000Scheduled The 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.

Charleston, SC30+ days ago

$37,200–$48,300 Per Year

Entity & 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.

Charleston, SC11 days ago

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. Addition Knowledge, Skills, Ability Preferred: The applicant should have a strong academic record, must be creative, self-driven, reliable, and motivated to learn.

Charleston, South Carolina11 days ago

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 Carolina participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees.

Charleston, South Carolina18 days ago

35%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.

Charleston, South Carolina19 days ago

Charleston, South Carolina30+ days ago

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. 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.

Charleston, South Carolina30+ days ago

Studies 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.

Charleston, SC30+ days ago

Preferred Experience, Knowledge, and Skills: Experience 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.

Charleston, South Carolina21 days ago

Examples 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.

Charleston, South Carolina24 days ago

Examples 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 targetsPreferred 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.

Charleston, South Carolina7 days ago

$33,339–$47,509 Per Year

Specifically, 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.

Charleston, South Carolina30+ days ago

30% - 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.

Charleston, SC30+ days ago

Charleston, SC30 days ago

Establish 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.

New!

Charleston, South Carolina4 days ago

Prior research experience in a lab, knowledge of REDCap data entry, management, reporting tools, interviewing research participants, conducting structured clinical interviews, neuropsychological tests and collecting biospecimens – including drawing blood and MRI assessments not required but valued. Applies technical knowledge to: Organize and coordinate biospecimen shipping and prepare reports for the Program Manager as needed; Support functional and structural MRI sessions and data transfer, troubleshoot issues arising during clinical sessions and scanning, and develop alternative approaches.

Charleston, South Carolina10 days ago

The incumbent will oversee, coordinate and assist in the screening, recruitment and enrollment of research participants, the collection of psychological and biological research data, data entry on case report forms and electronically, and organizational tasks including study status updates for the Principal Investigator in the Department of Psychiatry and Behavioral Sciences. 5% - Conduct study visits and/or recruitment outreach after regular work hours or off campus when necessary to accommodate participants’ schedules, ability to travel, and sites for recruitment.

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Clinical Research Jobs in Charleston, SC

Senior Clinical Research Associate ICON Plc

UNIV - Clinical Research Sponsor Invoicing Analyst - Office of Clinical Research, OVPR Medical University of South Carolina

Clinical Trial Liaison / Clinical Research Lead ICON Plc

Clinical Research Coordinator Alcanza Clinical Research LLC

Per Diem Clinical Research Nurse - Home Visits Science 37

Clinical Research Patient Recruitment Supervisor Alcanza Clinical Research LLC

Clinical Research Coordinator Alcanza Clinical Research

Clinical Research Patient Recruitment Supervisor Alcanza Clinical Research

Per Diem Clinical Research Nurse - Home Visits Science 37 Inc

UNIV - Clinical Research Coordinator - Department of Medicine: Division of Pulmonary Medical University of South Carolina

Clinical Research Physician (part time) - Metabolic: Endocrine, Hepatology, GI, Gen Med Alcanza Clinical Research LLC

Clinical Research Physician - Internal Medicine - Full time (32-40 hours per week) Alcanza Clinical Research LLC

Clinical Research Physician - Internal Medicine - Full time (32-40 hours per week) Alcanza Clinical Research

UNIV - Research Grant & Regulatory Coordinator - Surgery: Clinical Trials MUSC

UNIV - Research Grant & Regulatory Coordinator - Surgery: Clinical Trials Medical University of South Carolina

Nurse Practitioner or Physician Assistant - Psych: Sleep, Mood, Anxiety Research & Treatment (SMART) Medical University of South Carolina

UNIV - Open Rank Research Faculty - Surgery Medical University of South Carolina

UNIV - Open Rank Research Faculty - Surgery MUSC

UNIV - Program Manager I – Clinical Trials, Heart Failure - Department of Medicine: Division of Cardiology MUSC

UNIV - Program Manager I – EP, Structural & Preventative Cardiology Clinical Trials - Department of Medicine: Division of Cardiology MUSC

UNIV - Program Manager I - EP, Structural & Preventative Cardiology Clinical Trials - Department of Medicine: Division of Cardiology Medical University of South Carolina

UNIV - Program Manager I - Clinical Trials, Heart Failure - Department of Medicine: Division of Cardiology Medical University of South Carolina

UNIV - Program Manager I – Clinical Trials, Heart Failure - Department of Medicine: Division of Cardiology Medical University of South Carolina

UNIV - Research Finance Billing Compliance Analyst - Hollings Cancer Center MUSC

UNIV - Research Finance Billing Compliance Analyst - Hollings Cancer Center Medical University of South Carolina

UNIV - Research Assistant - Journey - Pediatrics: PRG Medical University of South Carolina

UNIV - Research Assistant - Journey - Pediatrics: PRG MUSC

UNIV - Research Program Assistant: Journey - Pediatrics: PRG Medical University of South Carolina

UNIV - Research Regulatory Specialist - Hollings Cancer Center Medical University of South Carolina

UNIV - Research Specialist III - Pharmacology & Immunology MUSC

UNIV - Research Specialist I - Department of Biochemistry MUSC

UNIV - Statistical Research Analyst - Orthopaedic Spine - Department of Orthopaedics MUSC

UNIV - Research Specialist III - Pharmacology & Immunology Medical University of South Carolina

UNIV - Research Specialist I - Department of Dermatology Medical University of South Carolina

UNIV - Research Specialist I - Department of Pharmacology & Immunology Medical University of South Carolina

UNIV - Statistical Research Analyst I - Hand and Upper Extremity - Department of Orthopaedics Medical University of South Carolina

UNIV - Statistical Research Analyst I - Hand and Upper Extremity - Department of Orthopaedics MUSC

UNIV - TSL Shared Resources Research Specialist - Hollings Cancer Center MUSC

UNIV - TSL Shared Resources Research Specialist - Hollings Cancer Center Medical University of South Carolina

UNIV - Research Specialist I - Department of Biochemistry Medical University of South Carolina

UNIV - Research Specialist III - Department of Pharmacology Medical University of South Carolina

UNIV - Research Specialist I - Department of Medicine: Division of Rheumatology Medical University of South Carolina

UNIV - Assistant Director of Community Site Research - Hollings Cancer Center MUSC

UNIV - Assistant Director of Community Site Research - Hollings Cancer Center Medical University of South Carolina

UNIV – Research Specialist I – Department of Pharmacology & Immunology MUSC

UNIV - Research Specialist I - Department of Neurosciences MUSC

UNIV - Research Specialist I - Department of Neurosciences Medical University of South Carolina

Deputy CIO, Academic and Research Technology - Information Solutions Medical University of South Carolina

UNIV - Research Program Coordinator I - Psychiatry: Addiction Sciences Division Medical University of South Carolina

UNIV - Research Program Assistant - Psychiatry: Admin MUSC

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