Research Assistant ProPharma Group Holdings LLCResearch AssistantRaleigh, NCWith deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs. For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies.
Case Manager SE Advocate Health and Hospitals CorporationCase Manager SEWake Forest, North CarolinaHe/she collaborates with a patient care team that includes, but is not limited to physicians, nurses and assistive staff, rehabilitative therapies, respiratory therapy, pharmacy, dietetics, psychosocial support disciplines, infection control, fiscal services, performance improvement, and any other disciplines directly and indirectly involved in patient care. Providing care under the names Advocate Health Care in Illinois; Atrium Health in the Carolinas, Georgia and Alabama; and Aurora Health Care in Wisconsin, Advocate Health is a national leader in clinical innovation, health outcomes, consumer experience and value-based care.
Manager Biosample Operations #4899 GrailManager Biosample Operations #4899Durham, NC$100,000–$133,000 / yearWe have built a multi-disciplinary organization of scientists, engineers, and physicians and we are using the power of next-generation sequencing (NGS), population-scale clinical studies, and state-of-the-art computer science and data science to overcome one of medicine's greatest challenges. The Manager, Biorepository Operations provides leadership and oversight for the organization's on-site and off-site biorepository operations, ensuring operational excellence, regulatory compliance, and alignment with organizational goals.
NewFDA IND-IDE Specialist University of North Carolina at Chapel HillFDA IND-IDE SpecialistChapel Hill, NCDepartment Research Compliance Services - 620200 Career Area Research Professionals Posting Open Date 08/31/2026 Application Deadline 09/03/2026 Position Type Temporary Staff (SHRA) Position Title FDA IND-IDE Specialist Position Number 20078418 Vacancy ID S028020 Full-time/Part-time Part-Time Temporary Hours per week 16 Work Schedule Position Location North Carolina, US Hiring Range $30.00 per hour Proposed Start Date 10/01/2026 Estimated Duration of Appointment 1 to 6 months. The temporary FDA IND/IDE Specialist is responsible for the organization, coordination, review, and submission of regulatory documents supporting Investigational New Drug (IND) applications, Investigational Device Exemption (IDE) applications, amendments, supplements, annual reports, and related FDA communications.
Director of Business Development M3 USA CorpDirector of Business DevelopmentRaleigh, NCRemoteM3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs). As of today, our board-certified physicians have completed more than 7,000+ successful clinical trials, while consistently exceeding sponsor expectations for integrity, timeliness, subject enrollment, human protection, and expeditious delivery of accurate evaluable data.
Global Clinical Trial Leader - FSP ParexelGlobal Clinical Trial Leader - FSPNorth CarolinaThe CTL provides leadership and direction to the trial team (core and extended team members) and is accountable for the overall success and delivery of their assigned clinical trial according to defined milestones and key performance indicators. CTLs are accountable for the set-up, execution and delivery of their assigned trial(s) and contribute to delivery of client’s pipeline through accurate planning and efficient execution of trials that bring speed and value to participating subjects and sites.
Research Faculty - Center for Sleep & Circadian Rhythms - Wake Forest University School of Medicine (WFUSM) Advocate Health and Hospitals CorporationResearch Faculty - Center for Sleep & Circadian Rhythms - Wake Forest University School of Medicine (WFUSM)Wake Forest, North CarolinaProviding care under the names Advocate Health Care in Illinois, Atrium Health in the Carolinas, Georgia and Alabama, and Aurora Health Care in Wisconsin, Advocate Health is a national leader in clinical innovation, health outcomes, consumer experience and value-based care, with Wake Forest University School of Medicine serving as the academic core of the enterprise. Create a centralized resource of sleep and rhythms expertise and technologies for use throughout the Enterprise (both research and clinical domains), and serve as a coordinating ‘hub’ for bringing together different investigators and organizational units involved in sleep- and rhythms-related research and clinical practice.
Director, Enterprise Epic Applications- Clinical - SolutionHealth - Full Time SolutionHealthDirector, Enterprise Epic Applications- Clinical - SolutionHealth - Full TimeNCThis role provides deep domain leadership for Epic and tightly integrated third party clinical and ancillary systems that enable safe, efficient, and high-quality clinical workflows, including documentation, orders, clinical decision support, ancillary services, and care coordination within the clinical record. Provides strategic leadership for Epic and third-party clinical applications supporting inpatient, ambulatory, home care, and ancillary care delivery, including clinical documentation, orders, results, clinical decision support, and specialty workflows across the continuum of care.
Development Technologist or Research Technician, Rotational Program Locus BiosciencesDevelopment Technologist or Research Technician, Rotational ProgramResearch Triangle Park, North CarolinaDesign and deploy automated workflows for molecular biology and microbiology assays, including liquid handling automation, next-generation sequencing (NGS) library preparation, and high-throughput screening of phage activity to accelerate research timelines and improve experimental reproducibility. The Locus platform engineers bacterial viruses called bacteriophages to specifically kill target pathogens while leaving non-target bacteria (i.e., the rest of the patient’s microbiome) unharmed and to deliver biotherapeutic payloads to the body sites where they are needed.
Open Rank University of North Carolina at Chapel HillOpen RankChapel Hill, NCDepartment Medicine-Internal Medicine - 411430 Posting Open Date 06/01/2026 Application Deadline Open Until Filled Yes Position Type Permanent Faculty Working Title Open Rank Appointment Type Open Rank Vacancy ID FAC0005961 Full-time/Part-time Full-Time Permanent Hours per week 40 FTE 1 Position Location North Carolina, US Hiring Range Proposed Start Date 01/01/2027. Patient care: The Palliative Care & Hospice Program, in partnership with the medical faculty of the School of Medicine, promotes health and provides superb clinical care while maintaining our strong tradition of reaching underserved populations and improving access to high quality healthcare across North Carolina and beyond.
Research Assistant ProPharma GroupResearch AssistantRaleigh, North CarolinaWith deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs. For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies.
Flex Nurse Educator - New Orleans, LA IQVIAFlex Nurse Educator - New Orleans, LADurham, LouisianaRemoteIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
Flex Nurse Educator - Indianapolis, IN IQVIAFlex Nurse Educator - Indianapolis, INDurham, IndianaRemoteIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
Flex Nurse Educator - Miami, FL IQVIAFlex Nurse Educator - Miami, FLDurham, FloridaRemoteIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
Flex Nurse Educator - Lakeland, FL IQVIAFlex Nurse Educator - Lakeland, FLDurham, FloridaRemoteIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
Flex Nurse Educator - San Antonio E, TX IQVIAFlex Nurse Educator - San Antonio E, TXDurham, TexasRemoteIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
Director, Regulatory Affairs CMC ProPharma Group Holdings LLCDirector, Regulatory Affairs CMCRaleigh, NCThe Director, Regulatory Affairs - Chemistry, Manufacturing, and Controls (CMC) is a senior-level contractor role responsible for defining and executing global CMC regulatory strategies across Dyne's development programs, from early-stage development through commercialization and post-approval lifecycle management. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs.
Senior Medical Writer - FSP ParexelSenior Medical Writer - FSPNorth CarolinaServe as the Medical Writing representative on assigned project teams and demonstrate document leadership: communicate content requirements, coordinate and conduct interdepartmental team review of draft and final documents, schedule and lead/facilitate authoring team meetings to agree on expectations, evaluate progress on tasks, identify issues and facilitate resolutions, manage/drive the timeline, and advance document development to approval, according to Parexel or client guidelines/SOPs. Gather, review, analyze, and evaluate pertinent resources to prepare, develop, and finalize clinical documents for submission to regulatory authorities, including but not limited to: briefing documents, investigator brochures, study protocols, model informed consents, interim and final clinical study reports, common technical document (CTD) clinical overviews and summaries, safety update/aggregate reports, and integrated summaries of safety and efficacy.
Senior Clinical Project Manager Azurity Pharmaceuticals IncSenior Clinical Project ManagerRaleigh, NCEnsures all clinical trials are executed in compliance with ICH/GCP guidelines/regulations and applicable SOPs: participates in the planning of quality assurance activities and coordinates resolution of audit findings; ensures audit-ready condition of clinical trial documentation including central clinical files, Trial Master File (TMF), and clinical trial registry submissions. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline.
Clinical Supervisor (SUD) - Sign-On Bonus $2,000 Steadfast HealthClinical Supervisor (SUD) - Sign-On Bonus $2,000Raleigh, North CarolinaYou must hold at least one of the following: LCSW (NC) with a minimum of 2 years of post-licensure clinical practice and an MSW from a CSWE-accredited program, in good standing with the NC Social Work Certification and Licensure Board — eligible to supervise LCSW Associates (LCSWA). Keywords: Clinical Supervisor · Behavioral Health Supervisor · LCSW · LCMHC · LCMHCS · LMFT · LMFT-S · LCAS · CCS · CCS-I · CADC · Substance Use Disorder · SUD · Addiction Treatment · Clinical Supervision · Raleigh, NC · Opioid Treatment Program · Player-Coach .