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. Charleston, South Carolina4 days ago
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.
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.
Charleston, SC30+ days ago
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.
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.
North Charleston, SC7 days ago
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.
Charleston, South Carolina8 days ago
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.
Greenville, SC30+ days ago
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.
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.
Spartanburg, SC5 days ago
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.
Charleston, SC22 days ago
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.
Columbia, South Carolina30+ days ago
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.
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.
Charleston, South Carolina30+ days ago
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;].
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.
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.
Spartanburg, SC25 days ago
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.
Charleston, SC30+ days ago
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.
Indian Land, SC30+ days ago
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.
Charleston, SC30+ days ago
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.
Charleston, South Carolina19 days ago
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.
Charleston, South Carolina14 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.Entity. For further information about the E-Verify program, please click here: http://www.uscis.gov/e-verify/employees.
Charleston, SC19 days ago
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.
Charleston, SC11 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.
Richland County, SC30+ days ago
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.
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.
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.
Greenville, South Carolina30+ days ago
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. 
.
li>Coordinate, with supervision, assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing, and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports. Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites.
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.
North Charleston, SC18 days ago
li>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.
Greenville, SC12 days ago
We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
Greenville, SC30+ days ago
Responsible for the implementation, management and oversight of clinical trial research studies including the education of research staff, healthcare team member, participants and their caregivers. Coordinates industry sponsored clinical trials by implementing sponsor provided protocols, completing required regulatory submissions, and ensuring adherence to study procedures and timelines.
ul>Performs the full scope of Registered Dietitian practices; including, but not limited to, providing virtual lifestyle counseling visits to improve nutrition and dietary quality, mental health and developing coping skills, and building health behavior and lifestyle habits that align with participant’s goals and values. Works cooperatively with Clinical Project Manager and site personnel to complete visits and submit accurate source documents in a timely manner.
Charleston, South Carolina27 days ago
The Research Specialist III of the Medical University of South Carolina (MUSC) Hollings Cancer Center (HCC) Translational Science Laboratory (TSL) Shared Resource core performs various experimental procedures including operating and maintaining complex scientific instruments at the core.Entity.
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.
Charleston, South Carolina26 days ago
p/>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. The Research Specialist III of the Medical University of South Carolina (MUSC) Hollings Cancer Center (HCC) Translational Science Laboratory (TSL) Shared Resource core performs various experimental procedures including operating and maintaining complex scientific instruments at the core.
Entity.
Charleston, South Carolina19 days ago
The candidate will assist the Principal Investigator in the recruitment of research participants, the collection of psychological research data, data entry and organizational tasks for studies being conducted in the Department of Psychiatry/Addiction Sciences Division. For further information about the E-Verify program, please click here: http://www.uscis.gov/e-verify/employees.
Charleston, SC19 days ago
p>The candidate will assist the Principal Investigator in the recruitment of research participants, the collection of psychological research data, data entry and organizational tasks for studies being conducted in the Department of Psychiatry/Addiction Sciences Division. 20% Initiate and maintain accurate and comprehensive documentation as required by FDA, Institutional Review Board, study sponsors and Good Clinical Practice Guidelines in connection with research trials.
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.
Lancaster, SC30+ days ago
li>Performs routine activities such as facilitating site recruitment, site training and study initiation, in-life and close-out activities in order to ensure site activities are in accordance with project objectives. Minimum Education:
- Masters degree preferably in animal science, biology, veterinary, or related life science with 4+ years of experience with a producer of nutraceutical or pharmaceutical products.
Charleston, SC30+ days ago
Edwards College of Dental Medicine seeks a dynamic and innovative Assistant Professor to develop an independent, externally funded research program focused on wound healing, musculoskeletal repair and regeneration, with a complementary emphasis on alveolar bone regeneration and craniofacial biology. Position Summary:
The Department seeks a dynamic and innovative Assistant Professor to develop an independent, externally funded research program focused on wound healing, musculoskeletal repair and regeneration, with a complementary emphasis on alveolar bone regeneration and craniofacial biology.
Charleston, South Carolina30+ days ago
Edwards College of Dental Medicine seeks a dynamic and innovative Assistant Professor to develop an independent, externally funded research program focused on wound healing, musculoskeletal repair and regeneration, with a complementary emphasis on alveolar bone regeneration and craniofacial biology. The Department seeks a dynamic and innovative Assistant Professor to develop an independent, externally funded research program focused on wound healing, musculoskeletal repair and regeneration, with a complementary emphasis on alveolar bone regeneration and craniofacial biology.
You will complete a short screening form so our system can match you with relevant consumer research opportunities within our national insights program. All tasks are conducted online and can be completed outside traditional business hours.
Charleston, South Carolina19 days ago
li>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
p>The Sleep, Mood, Anxiety Research & Treatment (SMART) Division within the Department of Psychiatry and Behavioral Sciences at the Medical University of South Carolina (MUSC) in Charleston, SC is seeking a full-time faculty member to provide evidence-based outpatient treatment for a wide spectrum of sleep, anxiety or mood disorders, including common co-morbid sensory processing conditions (tinnitus, eating, smell & taste disturbances). The Sleep, Mood, Anxiety Research & Treatment (SMART) Division within the Department of Psychiatry and Behavioral Sciences at the Medical University of South Carolina (MUSC) in Charleston, SC is seeking a full-time faculty member to provide evidence-based outpatient treatment for a wide spectrum of sleep, anxiety or mood disorders, including common co-morbid sensory processing conditions (tinnitus, eating, smell & taste disturbances).
li>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.