356 Results for

Clinical Research Manager Jobs in South Carolina

Jobs

Spartanburg, SC

Remote

Full time

p>The Inside Sales Specialist is responsible for identifying, qualifying, and nurturing potential customers interested in real-world data solutions for healthcare, life sciences, and related research markets. • Proactively identify and qualify potential customers for RWD products and services via outbound calls, emails, and digital outreach.

8 days ago

Greenville, SC

Experience - Two (2) years of Allied health, medical or research related experience In Lieu Of In lieu of education and experience noted above, equivalent combination of work/academic experience may be considered (i.e., Bachelor's degree in clinical, healthcare or scientific related field of study) Required Certifications, Registrations, Licenses SoCRA or ACRP certification - Preferred Oncology medical research experience - Preferred Some medical office experience preferable in oncology - Preferred Knowledge, Skills and Abilities Computer skills (word processing, spreadsheets, database, data entry) Medical terminology knowledge - Preferred Work Shift Day (United States of America) Location Cancer Centers - Faris Road Facility 1008 Greenville Memorial Hospital Department 10559220 OP Oncology Research-CIF Share your talent with us! Compiles medical records of research subjects during the on-study, treatment and follow-up periods and reports required elements to the research sponsor in a complete, accurate and timely manner.

30+ 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.

30+ days ago

Charleston, SC

$50–$55 / hour

17 days ago

North Charleston, SC

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.

13 days ago

Charleston, South Carolina

14 days ago

Charleston, South Carolina

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.

30+ days ago

Charleston, South Carolina

30+ days ago

Charleston, South Carolina

30+ days ago

Charleston, SC

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.

30+ days ago

Charleston, SC

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.

30+ days ago

North Charleston, SC

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.

30+ days ago

Charleston, South Carolina

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.

30+ days ago

North Charleston, SC

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.

30+ days ago

Charleston, SC

Remote

Your previous roles/job titles may include Clinical Data Manager, Senior Clinical Data Manager, Lead Data Manager, Principal Data Manager, and/or Data Management Project Manager. IQVIA is seeking experienced Clinical Data Management Leads to oversee end-to-end data management delivery for global clinical trials.

30+ 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

Charleston, South Carolina

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

Columbia, SC

$124,000–$280,000 / year

p>PwC does not intend to hire experienced or entry level job seekers who will need, now or in the future, PwC sponsorship through the H-1B lottery, except as set forth within the following policy: https://pwc.to/H-1B-Lottery-Policy.

As a Payer STARS/Quality Clinical Consultant, Senior Manager, you will engage with clients in the health services sector, providing strategic guidance and operational consulting to enhance their clinical quality and performance metrics.

2 days ago

Greenville, South Carolina

Primary responsibilities include recruiting and monitoring study participants, maintaining research materials required for coordinating projects, protocol compliance, assisting research investigators in developing and completing research projects. Bon Secours seeks people that are committed to our values of compassion, human dignity, integrity, service and stewardship to create an environment where associates want to work and help communities thrive.

30+ days ago

Richland County, SC

Clickhttps://nam02.safelinks.protection.outlook.com/?url=https%3A%2F%2Fsc.edu%2Fabout%2Foffices_and_divisions%2Fhuman_resources%2Fcareers%2Findex.php&data=05%7C01%7CKURTRS%40email.sc.edu%7Ceca45df616784275e15908dab2a706ac%7C4b2a4b19d135420e8bb2b1cd238998cc%7C0%7C0%7C638018727680845870%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=j6sQGvabHDZHDmRBFwMrq8P8QCuDmChuJ%2FH5%2F8hDRUw%3D&reserved=0 to learn more about why you should work at USC . The University of South Carolina College of Nursing invites applications for a full-time, on-site Research Program Manager To provide strategic and operational leadership for the Center for Advancing Chronic Care Outcomes through Research and Innovation (ACORN ) portfolio of funded and unfunded research activities.

30+ days ago

Columbia, SC

Logo Posting Number STA00244PO26 Job Family Research Job Function Research Program Management USC Market Title Research Program Manager Link to USC Market Title https://uscjobs.sc.edu/titles/133775 Job Level M0 - Managerial Business Title (Internal Title) Research Program Manager Campus Columbia Work County Richland College/Division College of Nursing Department CON College of Nursing State Pay Range G11 USC Market Range MRI - $69,913 $87,391 $104,870 Anticipated Hiring Range Salary commensurate with qualifications Location of Vacancy Part/Full Time Full Time Hours per Week 37.5 Work Schedule. The University of South Carolina College of Nursing invites applications for a full-time, on-site Research Program Manager To provide strategic and operational leadership for the Center for Advancing Chronic Care Outcomes through Research and Innovation (ACORN) portfolio of funded and unfunded research activities.

30+ days ago

Lancaster, SC

$78,900–$106,300 / year

Current BLS (Basic Life Support) required • Planning, organization, prioritization and time-management skills • Strong interpersonal, oral and written communication skills, to include presentation skills • Ability to work with others in a team environment and to communicate in laymen's terms at all levels of the organization • Ability to work on multiple projects at the same time • Strong customer service skills and follow-up skills • Strong analytical and quantitative skills • Leadership skills • Team-building and motivational skills • Research and teaching skills • Change management and demonstrated problem-solving skills • Proficiency in Microsoft Suite (Excel, Word, Outlook, Power Point) preferred • Working knowledge of systems/applications in hospital databases and web-based databases • Physical Demands: • Being in a stationary position for extended periods of time (4 hours or more) • Viewing computer screen for extended periods of time (4 hours or more) • Keying frequently on a computer for 4 hours or more • Moving about • Close, distance and peripheral vision • Reading • Communicating • Writing • Lifting/moving items up to 20 pounds • Lifting/moving items up to 75 pounds with equipment assistance • Pushing/pulling • Bending/stooping • Reaching/grasping/touching with hands • Traveling distances (car, airplane, etc.). • Organizes and prioritizes clinical responsibilities, provides clinical oversight to clinical staff, such as Registered Nurses (RNs); Licensed Practical Nurses (LPNs) or Licensed Vocational Nurses (LVNs); Certified Medical Assistants (CMAs); Hyperbaric Oxygen Technicians, etc.

30+ days ago

Conway, SC

$70,600–$95,100 / year

Organizes and prioritizes clinical responsibilities, provides clinical oversight to clinical staff, such as Registered Nurses (RNs); Licensed Practical Nurses (LPNs) or Licensed Vocational Nurses (LVNs); Certified Medical Assistants (CMAs); Hyperbaric Oxygen Technicians, etc. May be required to provide case management to a group of patients providing specific assessments according to protocols and procedures, clinical competence in procedural skills, treatments, and patient/caregiver education related to wound care management.

22 days ago

Summerville, SC

$78,900–$106,300 / year

p>• Current BLS (Basic Life Support) required • Planning, organization, prioritization and time-management skills • Strong interpersonal, oral and written communication skills, to include presentation skills • Ability to work with others in a team environment and to communicate in laymen's terms at all levels of the organization • Ability to work on multiple projects at the same time • Strong customer service skills and follow-up skills • Strong analytical and quantitative skills • Leadership skills • Team-building and motivational skills • Research and teaching skills • Change management and demonstrated problem-solving skills • Proficiency in Microsoft Suite (Excel, Word, Outlook, Power Point) preferred • Working knowledge of systems/applications in hospital databases and web-based databases • Physical Demands: • Being in a stationary position for extended periods of time (4 hours or more) • Viewing computer screen for extended periods of time (4 hours or more) • Keying frequently on a computer for 4 hours or more • Moving about • Close, distance and peripheral vision • Reading • Communicating • Writing • Lifting/moving items up to 20 pounds • Lifting/moving items up to 75 pounds with equipment assistance • Pushing/pulling • Bending/stooping • Reaching/grasping/touching with hands • Traveling distances (car, airplane, etc.). • Organizes and prioritizes clinical responsibilities, provides clinical oversight to clinical staff, such as Registered Nurses (RNs); Licensed Practical Nurses (LPNs) or Licensed Vocational Nurses (LVNs); Certified Medical Assistants (CMAs); Hyperbaric Oxygen Technicians, etc.

30+ days ago

Conway, South Carolina

23 days ago

Lancaster, South Carolina

17 days ago

$103,400–$149,430 / year

Preferred Qualifications: • Experience in clinical practice with a focus in appeals & grievances, claims processing, utilization review or utilization management/case management • Demonstrated understanding of Utilization Review Guidelines (NYS ART 44 and 49 PHL), InterQual, Milliman or Medicare local coverage guidelines • Extensive experience in healthcare appeals • MBA or master's degree from an accredited institution with focus in training & development, education, business, or healthcare administration • Management experience in an operational department within the healthcare industry focused on clinical leadership • Leadership experience in a focus area of operational excellence or audit • Experience developing strategy and processes for a department or function • Experience managing vendors as an extension of a core team • Familiar with creating accountable ownership of a vendor team. Minimum Qualifications: • Bachelor's degree from an accredited institution or equivalent work experience • RN • Experience with utilization management or appeals and grievance processing and compliance • Working experience in a fast-paced environment overseeing multiple priorities, tasks and/or teams • Proven track record of exercising independent thinking, ability to problem solve, understand process flows and correlating platforms to recommend and implement solutions • Experience preparing and delivering written and verbal information to multiple types of audiences • Demonstrated ability to build and foster effective relationships.

30+ days ago

Greenville, SC

30+ days ago

Columbia, SC

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.

30+ days ago

Columbia, South Carolina

Provides patients/families with information regarding clinical trial participation and provides education regarding individual treatment including purpose, potential side effects, and self-care measures, documents interaction. Collaborates with the IRB of record and sponsoring agencies as well as local agencies, when applicable, to ensure global awareness regarding the progression of various studies, amendments and regulatory monitoring.

30+ days ago

Greenville, SC

27 days ago

Lancaster, SC

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.

30+ days ago

Columbia, SC

20 days ago

Columbia, South Carolina

16 days ago

Charleston, South Carolina

Under general supervision of the Clinical Trials Office (CTO) and specific disease group Program Manager within the Clinical Operations Unit, this position coordinates, establishes, and supervises complex research protocols at the Hollings Cancer Center (HCC) to efficiently and effectively integrate the National Cancer Institute (NCI), investigator initiated and industry sponsored oncology trials at the Medical University of South Carolina (MUSC). Under guidance of the team lead coordinator(s) and program manager, will support research activities at any of the MUSC main campus and HCC satellite locations and make necessary coverage plans in advance, to avoid interruption of quality CTO services.

2 days ago

Charleston, SC

p>Summary:

2 days ago

Charleston, SC

$39,764–$56,670 / 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.

30+ days ago

Charleston, SC

$127,530–$236,841 / year

Built on a 70-year plus commitment to science and research, Ferring is relentless in its pursuit of science that drives powerful discoveries and therapies to help people build families, stay healthy, and stand up to the world's oldest enemy: disease. With Ferring, you will be joining a recognized leader, identified as one of "The World's Most Innovative Companies" by Fast Company, and honored by Fortune with inclusion on its "Change the World List," for addressing society's unmet needs.

30+ days ago

CHARLESTON, South Carolina

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.

30+ days ago

Charleston, SC

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.

30+ days ago

Columbia, SC

p>Position Description Advertised Job Summary Community Health Worker will work with licensed research nurse RN and other team members to assist in coordinating and delivering a telehealth/remote intervention with patients with chronic health conditions, as well as their Carepartners for a research study funded by the National Institutes of Health (NIH) that seeks to improve current and future chronic illness management among adults and their caregivers in medically underserved and rural areas of South Carolina. Ability to work with a level of independence and also in concert with the research team, patients, and their respective care partners to operationalize the devised wellness goals/plans by providing resource navigation, coordination, referral assistance, and facilitating access to care and other community resources.

30+ 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.

2 days ago

Charleston, South Carolina

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.

21 days ago

Charleston, South Carolina

22 days ago

Charleston, South Carolina

Coordinate/perform the reporting and communications with the IRB, government agencies and study sponsors regarding adverse effects, study implementations, study renewals, study terminations, study close-out and other activities necessary for exceptional performance of all studies from inception to close. 25%: Coordinate proper data management according to protocol requirements and protocol compliance, i.e. collect and record all data pertaining to study patients on specific (funded or unfunded) studies and submit on time to research bases.

15 days ago

Charleston, South Carolina

16 days ago

Greenville, SC

$80,000–$100,000 / year

Identify, define, and execute on market opportunities by implementing new marketing strategies, developing effective sales plans, and achieving balanced revenue growth from all customer accounts through targeted sales channels (hospitals, medical centers, surgical centers and related entities) within assigned territory. Promote and sell the Company's surgical products and tissues by interacting with established agency partners, customers and developing new prospects (agent partners and customers).

13 days ago

Charleston, SC

Maintains all incoming payments, including but not limited to: preparing ACH Wire and Check Deposit forms to ensure that the funds hit the correct accounts; reviewing the unclaimed cash report and completes the necessary forms to claim the funds earned by the program; communicating with sponsors to secure supporting documentation, if needed; Responsible for ensuring all activities are in compliance with Federal, State, and Institutional policies and award specific regulations and requirements. Works closely with Department Leadership and Grant and Finance colleagues to proactively submit cost allocations, ASWs, and payroll accounting adjustments in OurDay as needed, while ensuring accurate accounting of research effort and adherence to divisional funds flow plan.

30+ days ago

$139,100–$231,900 / year

Identify and explore areas where real‑world clinical practice, systems of care, or patient experience may diverge from established evidence, guidelines, or evolving scientific understanding, and engage customers in scientific dialogue to better understand contributing factors and potential opportunities for improvement. Support patient‑focused discussions that highlight unmet needs, variability in care delivery, and barriers to optimal outcomes across diverse care settings, ensuring engagements remain grounded in scientific evidence and compliant medical exchange.

27 days ago

$189,200–$315,400 / year

27 days ago

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Clinical Research Manager Jobs in South Carolina

Inside Sales Specialist - REMOTE Guardian Research Network

Clinical Research Coordinator, Oncology Research, Full Time, Days Prisma Health

Per Diem Clinical Research Nurse - Home Visits Science 37 Inc

Per Diem Clinical Research Nurse - Home Visits Science 37

Clinical Research Patient Recruitment Supervisor Alcanza Clinical Research LLC

Clinical Research Patient Recruitment Supervisor Alcanza Clinical Research

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 MUSC

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

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

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

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

Lead Clinical Data Manager (Remote) IQVIA Holdings Inc

Clinical Research Coordinator Alcanza Clinical Research LLC

Clinical Research Coordinator Alcanza Clinical Research

Payer STARS/Quality Clinical Consultant, Senior Manager PricewaterhouseCoopers LLP

Registered Nurse (RN) - Clinical Research - Upstate Cardiology Bon Secours Mercy Health

Research Program Manager State of South Carolina

Research Program Manager University of South Carolina

Clinical Nurse Manager - CNM - BSN Required Healogics Inc

Clinical Nurse Manager -Registered Nurse - BSN Preferred Healogics Inc

Clinical Nurse Manager - CNM Healogics Inc

Clinical Nurse Manager -Registered Nurse - BSN Preferred Healogics

Clinical Nurse Manager - CNM - BSN Required Healogics

Mgr Clinical Appeals and Grievances Healthfirst

Registered Nurse (RN) - Clinical Research - Upstate Cardiology Bon Secours Mercy Health Inc

Research Coordinator II, Cardiology Research, Full Time, Days Prisma Health

RN Research, Oncology Research, FT, Days Prisma Health

Research Coordinator II, Oncology, Full Time, Days Prisma Health

Research Scientist Nutramax Laboratories Inc

Registered Nurse (RN)- Research, Pediatric 9 Medical Park, FT, Day Prisma Health

Registered Nurse (RN)- Research, Pediatric Oncology 9 Medical Park , FT, Day Prisma Health

UNIV - Research Study Coordinator-Hollings Cancer Center MUSC

UNIV - Research Study Coordinator-Hollings Cancer Center Medical University of South Carolina

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

Manager, Medical Science Liaison, Uro Oncology - Mid-Atlantic Ferring Pharmaceuticals Inc

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

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

Research Program Coordinator I University of South Carolina

Research Assistant / Medical Assistant Alcanza Clinical Research LLC

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 Program Coordinator II - Journeyman - Department of Neurosurgery MUSC

UNIV - Research Program Coordinator II - Journeyman - Department of Neurosurgery Medical University of South Carolina

Surgical Territory Manager MiMedx Group Inc

UNIV - Finance Manager - Department of Medicine: Divisions of Cardiology & Endocrinology Medical University of South Carolina

Senior Manager, Field Medical, non-MD Pfizer Inc

Senior Manager, Field Medical, MD Pfizer Inc

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