89 Results for

1st Shift Research Jobs in South Carolina

Jobs

Dillon, SC

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30+ days ago

Anderson, SC

Provides direction to the Pelzer Point management team for the development and implementation of risk reduction solutions, safety best practices, and continuous improvements to drive to zero injuries.

Responsible for planning, implementing, and managing local Environmental, Health, and Safety (EHS) programs, projects, and initiatives to maintain compliance and promote a culture of safety at the Vertiv Anderson facility.

11 days ago

Moncks Corner, SC

Full time

What you need to succeed at GXO: At a minimum, you'll need: Ability to speak, read (fine print) and write in English, including reading, understanding and interpreting safety rules, operating instructions and procedural documents . Our greatest strength is our global team - energetic, innovative people of all experience levels and talents who make GXO a great place to work.

30+ days ago

Moncks Corner, SC

Full time

Our greatest strength is our global team - energetic, innovative people of all experience levels and talents who make GXO a great place to work. Excellent verbal and written communication skills; ability to present clean, organized and thorough information and data appropriate for intended audience.

30+ days ago

Simpsonville, South Carolina

Not Required

At RTX, the world largest aerospace and defense company, 185,000 great minds are united by purpose and inspired to make a difference solving the world’s most complex problems.

As part of our commitment to maintaining a secure hiring process, candidates may be asked to attend select steps of the interview process in-person at one of our office locations, regardless of whether the role is designated as on-site, hybrid or remote..

30+ days ago

Woodruff, SC

Objectives | Purpose: Receiving operation is responsible for accurately receiving product from the B&L Manufacturing Operation along with other third-party vendors, putting product into assigned storage locations, and retrieving product and delivering it to the pick area and/or shipping lanes. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe.

30+ days ago

Greenville, SC

We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe.

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world-from the moment of birth through every phase of life.

30+ days ago

North Charleston, SC

Provides support to customers in solving technical problems incurred in the installation or operation of company products; consults with customers regarding pre and post-installation problems; may review customer equipment interface requirements. This position frequently requires standing, walking, sitting, using hands, reaching, climbing, stooping, kneeling, crouching, crawling, talking, and hearing, as well as vision abilities including close, distance, color, peripheral, and depth perception, and focus adjustment.

28 days ago

Simpsonville, SC

Regardless of your role type, collaboration and innovation are critical to our business and all employees will have access to digital tools so they can work with colleagues around the world and access to Collins sites when their work requires in-person meetings. At RTX, the world largest aerospace and defense company, 185,000 great minds are united by purpose and inspired to make a difference solving the worlds most complex problems.

30+ days ago

Simpsonville, SC

Regardless of your role type, collaboration and innovation are critical to our business and all employees will have access to digital tools so they can work with colleagues around the world - and access to Collins sites when their work requires in-person meetings. At RTX, the world largest aerospace and defense company, 185,000 great minds are united by purpose and inspired to make a difference solving the world's most complex problems.

30+ days ago

Ladson, South Carolina

p style="margin:0px">Important Note:Some positions require additional screening that may include employment and education verification; motor vehicle records check and a road test; and/or badging or background requirements of the customer to which you are assigned.

At Ryder, you will be part of a team-first culture built on respect when joining a community of proud women and men in Supply Chain, including many Military Reservists and Veterans.

2 days ago

Duncan, SC

Utilize packing slips to generate print move tickets, breakdown material, sort styles, verify count and restock appropriate warehouse locations via use of LXE computers to scan material, styles, location and re-verify count. In this role, you will: Operate reach truck and order picker in order to retrieve appropriate styles and quantities of material from warehouse locations (often from varying levels of height) using appropriate picking process.

30+ days ago

Moncks Corner, SC

li>It'd be great if you also have: • Bachelor's degree in Occupational Health and Safety • Solid understanding of OSHA requirements is preferred • Solid time and project management skills with the ability to multitask and prioritize workloads • Solid skills in Microsoft Office applications. Our greatest strength is our global team - energetic, innovative people of all experience levels and talents who make GXO a great place to work.

30+ days ago

Duncan, SC

In this role, you will:

Operate reach truck and order picker in order to retrieve appropriate styles and quantities of material from warehouse locations (often from varying levels of height) using appropriate picking process.

9 days ago

Duncan, SC

After making a conditional offer and running a background check, if Eaton is concerned about conviction that is directly related to the job, you will be given the chance to explain the circumstances surrounding the conviction, provide mitigating evidence, or challenge the accuracy of the background report. Please note that specific programs and options available to an employee may depend on eligibility factors such as geographic location, date of hire, and the applicability of collective bargaining agreements.

22 days ago

Sumter, SC

The primary function of this role is to be responsible for providing manufacturing expertise and support in the Shipping area including, but not limited to, allocation of materials, planning, scheduling, verifying, receiving, and shipping in either the Front or Back Storeroom. After making a conditional offer and running a background check, if Eaton is concerned about conviction that is directly related to the job, you will be given the chance to explain the circumstances surrounding the conviction, provide mitigating evidence, or challenge the accuracy of the background report.

30+ days ago

Sumter, SC

30+ days ago

Sumter, SC

4 days ago

Moncks Corner, SC

p>What you need to succeed at GXO:

At a minimum, youll need:

Ability to speak, read (fine print) and write in English, including reading, understanding and interpreting safety rules, operating instructions and procedural documents. Our greatest strength is our global team - energetic, innovative people of all experience levels and talents who make GXO a great place to work.

30+ days ago

Fountain Inn, SC

As a wholly owned subsidiary of KYOCERA Corporation structured to capitalize on shared resources and technical expertise, KYOCERA AVX has an expansive global footprint comprised of several dozen research, development, and manufacturing facilities spanning more than 15 countries and staffed with talented personnel dedicated to innovation, component quality, customer service, and enabling a brighter future through technology. KYOCERA AVX designs, develops, manufactures, and supplies advanced capacitors, antennas, connectors, circuit protection and timing devices, sensors, controls, filters, fuses, diodes, resistors, couplers, and inductors optimized for employment in the international 5G, IoT, aerospace, automotive, consumer electronics, industrial, medical, and military markets.

30+ days ago

Fountain Inn, SC

KYOCERA AVX designs, develops, manufactures, and supplies advanced capacitors, antennas, connectors, circuit protection and timing devices, sensors, controls, filters, fuses, diodes, resistors, couplers, and inductors optimized for employment in the international 5G, IoT, aerospace, automotive, consumer electronics, industrial, medical, and military markets.

22 days ago

Fountain Inn, SC

30+ days ago

Charleston, SC

$52,100–$70,300 / 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.

30+ days ago

Myrtle Beach, SC

p>Qualifications:

Minimum of two years of experience as a licensed physician assistant, family or non-acute adult nurse practitioner treating a wide variety of therapeutic areas for the adult and geriatric patient population required (internal medicine, family medicine, urgent care, emergency medicine).
Dynamic Team Environment: You'll help Headlands Research continue to build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists.

30+ days ago

Myrtle Beach, South Carolina

div>

Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.

20 days ago

New
Charleston, SC
p>Job 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.
5 days ago

New
Charleston, South Carolina
ul>
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. For further information about the E-Verify program, please click here: http://www.uscis.gov/e-verify/employees.
5 days ago

Charleston, SC
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.
30+ days ago

Charleston, SC
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.
26 days ago

North Charleston, SC
Responsibilities 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.
8 days ago

Charleston, South Carolina
Responsibilities 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 . The Research Assistant (RA) 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.

9 days ago

North Charleston, SC
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.
30+ days ago

Greenville, SC
Employees in a FT or PT status (40+ hours per pay period) will also be eligible for paid time off, life insurance, short term and long-term disability and the Flexible Spending Account (FSA) plans and a Health Savings Account (HSA) if a High Deductible Health Plan (HDHP) is elected.
Greenville, South Carolina has been named among American's Best Small Cities by Condé Nast Traveler and one of the South's Best Cities on the Rise by Southern Living.
30+ days ago

Charleston, South Carolina
li>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;].

30+ days ago

New
Spartanburg, SC
Screens for potential patients for clinical trial opportunities, educating patients and families about research and, obtaining and developing research data, and monitoring compliance with research protocols.
· Current certification in clinical research (SOCRA-CCRP, ACRP-CCRC or ACRP-CP) with three years clinical research experience with human subjects.
6 days ago

Charleston, SC
$50–$55 / 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.
23 days ago

Columbia, South Carolina
div>Seeking a highly organized, detail-oriented Clinical Research Coordinator to join our team and bridge the gap between innovative medical research and compassionate patient care. You will work closely with our Principal Investigators (PIs), clinical staff, and industry sponsors to ensure that all research is conducted with the highest degree of integrity, compliance, and patient safety.
30+ days ago

Clemson, SC
p>SiteBridge Research Inc:
Founded in 2021, SiteBridge Research (SBR) is an integrated research organization, building a national network of small and community practices to deliver world-class industry sponsored clinical research on time and on budget, accelerating time to market and product adoption in communities that are hardest to reach. The role involves close collaboration with the site team, sponsors, and clinical monitors to ensure ICH/GCP compliance, optimize site efficiency, and support timely study completion.
12 days ago

Charleston, SC
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.
30+ days ago

Spartanburg, SC
Completes study documentation and maintains study files in accordance with sponsor requirements including, but not limited to, consent forms, source documentation, and note to file, case report forms, and investigational material accountability forms. ESSENTIAL DUTIES AND RESPONSIBILITIES: Coordinates with Principal Investigator, department, and administration to help ensure that clinical research and related activities are performed in accordance with Federal Regulations and sponsoring agency (pharmaceutical and or CRO) policies and procedures.
26 days ago

Clemson, SC
p>Founded in 2021, SiteBridge Research (SBR) is an integrated research organization, building a national network of small and community practices to deliver world-class industry sponsored clinical research on time and on budget, accelerating time to market and product adoption in communities that are hardest to reach. The role involves close collaboration with the site team, sponsors, and clinical monitors to ensure ICH/GCP compliance, optimize site efficiency, and support timely study completion.
13 days ago

Indian Land, SC
li>Not easily distracted: You have the ability to stay focused while running different protocols, resolving and submitting IRB responses and audit findings, tracking AE and SAE events, and maintaining eSource material for assigned studies.
ObjectiveHealth is a clinical research company that uses proprietary technology to:
Increase patient access to research trials within our communities,
Provide physicians with enhanced care options for current patients, and.
30+ days ago

Charleston, SC
For further information about the E-Verify program, please click here: http://www.uscis.gov/e-verify/employees. 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.
20 days ago

Charleston, SC
p>Entity 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.
30+ days ago

Charleston, South Carolina
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.
Entity. For further information about the E-Verify program, please click here: http://www.uscis.gov/e-verify/employees.
15 days ago

SC
li>
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.
30+ days ago

Richland County, SC
li>It is desirable that candidates demonstrate experience with: (i) analysis of microvascular function using wire myography; (ii) proficiency in small-animal (mouse) surgical techniques, including radiotelemetry device implantation; (iii) cardiac transthoracic echocardiography in mice to assess diastolic function, vascular remodeling (e.g., pulse wave velocity), and coronary artery flow; and (iv) in vivo endothelial cell reprogramming strategies.
Under limited supervision of the Principal Investigator (PI; Dr. Camilla Ferreira Wenceslau), the Research Assistant Professor will evaluate research projects for consideration in the Cardiovascular Translational Research Center (CTRC ) at the Department of Cell Biology and Anatomy (CBA ), School of Medicine Columbia and develop experiments in collaboration with the PI's laboratory on projects focused on cardiovascular physiology and pharmacology.
30+ days ago

Columbia, SC
p>Logo Posting Number: RTF00050PO21 USC Market Title: Research Assistant Professor Link to USC Market Title: [insert link] Business Title: Research Assistant Professor Campus: Columbia Work County: Richland College Division: College of Pharmacy Department: COP Drug Discovery and Biomedical Sciences Location of Vacancy: Part-time.
Under limited supervision of the Principal Investigator (PI), the Research Assistant Professor will evaluate research projects for consideration in the Center for Translational Therapeutics (CTT) - Drug Design and Synthesis Core (DDBS) department at the College of Pharmacy and develop synthetic routes and implement synthesis for compounds requested by the DDBS.
30+ days ago

New
Columbia, SC
p>Logo Posting Number STA00481PO26 Job Family Research Job Function Research Laboratory Management USC Market Title Research Laboratory Manager Link to USC Market Title https://uscjobs.sc.edu/titles/133738 Job Level M1 - Managerial Business Title (Internal Title) Lab Director, Biobehvrl Research Center Campus Columbia Work County Richland College/Division College of Nursing Department CON Biobehvrl Hlth Nrsng Sci Oper State Pay Range G10 USC Market Range MRH - $63,557 $79,446 $95,336 Anticipated Hiring Range 63,557 Location of Vacancy Columbia, SC Part/Full Time Full Time Hours per Week 37.5 Work Schedule.
Understanding of both theoretical and technical aspects of a diverse set of laboratory procedures to include the operation and maintenance of basic protein measurement (ELISA, Western Blot), DNA extraction, RNA extraction, cDNA synthesis, and PCR Quant studio real-time and digital PCR.
4 days ago

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1st Shift Research Jobs in South Carolina

Wastewater Manager - 1st Shift Perdue Farms Inc

EHS Technician-1st shift Vertiv Group Corp.

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Production Technician Supervisor - 1st Shift - Travel GXO Logistics Worldwide, LLC

Mechanical Assembler IV Lead - 1st Shift(Onsite) RTX

Distribution Associate I, 1st Shift Bausch & Lomb Inc

Accessory Operator I, 1st Shift Bausch & Lomb Inc

Field Support Technician - 1st Shift (Onsite) RTX Corp

Material Handling Lead V 1st Shift(Onsite) RTX Corp

Mechanical Assembler IV Lead - 1st Shift(Onsite) RTX Corp

Warehouse Administrative Assistant 1st Shift Ryder

Picker (Forklift Operator)-1st Shift Eaton Corporation Plc

EHS Senior Supervisor - 1st Shift GXO Logistics Inc

Picker (Forklift Operator) - 1st Shift Eaton Corporation Plc

Packer (Material Handler)- 1st Shift Eaton Corporation Plc

Material Handler 1st Shift Eaton Corporation Plc

Material Handler - 1st Shift Eaton Corporation Plc

Material Handler Back Storeroom (1st Shift) Eaton Corporation Plc

Clerk - 1st Shift GXO Logistics Inc

Production Supervisor - 1st Shift Kyocera AVX Components Corp

Engineering Technician - 1st Shift Kyocera AVX Components Corp

Production Operator 1st shift Kyocera AVX Components Corp

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

Nurse Practitioner or Physician Assistant - Clinical Research Headlands Research Inc

Nurse Practitioner or Physician Assistant - Clinical Research Headlands Research

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

UNIV - Clinical Research Assistant - Department of Medicine: Division of Pulmonary MUSC

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

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

Research Assistant / Medical Assistant Alcanza Clinical Research LLC

Research Assistant / Medical Assistant Alcanza Clinical Research

Clinical Research Coordinator Alcanza Clinical Research LLC

Clinical Research Coordinator I (Temp Position Tentatively July 20, 2026 July 20, 2027) Shriners Hospitals for Children

Clinical Research Coordinator Alcanza Clinical Research

Coord-Clinical Research Spartanburg Regional Healthcare System

Per Diem Clinical Research Nurse - Home Visits Science 37

Research Coordinator Midlands Neurology and Pain Associates, P.A.

Clinical Research Coordinator (Clemson, SC) SiteBridge Research Inc

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

Clinical Research Coordinator - Spartanburg, SC Advanced Dermatology & Cosmetic Surgery

Clinical Research Coordinator (Clemson, SC) SiteBridge Research, Inc.

Per Diem Clinical Research Nurse - Home Visits Science 37 Inc

Clinical Research Coordinator I ObjectiveHealth Inc

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

UNIV - Statistical Research Analyst - Orthopaedic Spine - Department of Orthopaedics Medical University of South Carolina

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

Senior Clinical Research Associate ICON Plc

Research Assistant Professor State of South Carolina

Research Assistant Professor University of South Carolina

Lab Director, Biobehvrl Research Center University of South Carolina

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