Inside Sales Development Account Manager Worldwide Clinical Trials Holdings IncInside Sales Development Account ManagerDurham, NC$50,500–$100,000 / yearYou must be comfortable engaging prospective clients using various methods (i.e., calls, emails, and social), working with your Business Development and Marketing partners, generating interest and qualifying prospects and opportunities before hand-off to business development.*. Leverage Social Selling techniques and tools to reach clients through digital channels, sharing information including Worldwide's services, web conferences, industry meetings, SME news, etc.
NewHOSPICE CLINICAL MANAGER - RN Liberty HealthHOSPICE CLINICAL MANAGER - RNBurlington, NCProvides direct patient care as necessary to include case management, Oasis care planning, assigning Care staff, and ensuring the efficient, effective utilization of existing staffing resource. That is why Liberty Hospice provides our hospice patients with state-of-the-art care and pain management services, delivered by our specially trained staff with emphasis on strength, dignity and compassion.
NewClinical Research Coordinator Revival Research Institute, LLCClinical Research CoordinatorCary, NCStrong computer proficiency including Microsoft Office (Word, Excel, Outlook); excellent verbal and written communication; ability to work independently, manage competing protocol deadlines, and assume ownership of assigned studies. Clinical Research Coordinators at Revival coordinate and manage multiple concurrent studies and support the Investigators and clinical staff with study-related tasks including, but not limited to: Responsibilities Screening, recruitment, and enrollment.
NewInternational Medical Graduate (IMG) - Clinical Research Coordinator Revival Research Institute, LLCInternational Medical Graduate (IMG) - Clinical Research CoordinatorCary, NCAdditional Qualifications: Database and computer skills: Microsoft Office (Word, Excel), Outlook, excellent verbal and written communication skills, ability to work independently and assume responsibility, excellent organizational skills, ability to meet data deadlines and maintain confidentiality. Education/ Training: International Medical Graduate; MBBS, BMBS, MBChC, MBBCh, MD, DO, MCM, DM, MCM, MMSc, MMedSc, MM, MMed, MS, MSurg, MChir, MCh, ChM, CM, MSc, DCM, DClinSurg, DMSc, DMedSc, DS, DSurg.
NewAdvanced Practice Provider (CNS) Clinical Nurse Specialist Pediatrics UVA HealthAdvanced Practice Provider (CNS) Clinical Nurse Specialist PediatricsRALEIGH, NCUVA Health is an integrated health system with a world-class academic medical center that includes a level 1 trauma center, a level IV NICU, the first NCI-designated Comprehensive Cancer Center in Virginia, and UVA Health Children's, the #1 pediatric hospital in Virginia. UVA Health consists of UVA Health University Medical Center, UVA School of Medicine, UVA School of Nursing, UVA Claude Moore Health Sciences Library, UVA Community Health, and UVA Physicians Group.
Director, Clinical Quality Assurance CellectisDirector, Clinical Quality AssuranceRaleigh, NCThe Director, Clinical Quality Assurance is primarily responsible for establishing and leading the Clinical QA function and providing independent oversight of Good Clinical Practices (GCP) activities to ensure compliance with FDA, EMA, ICH, and other applicable global and national regulatory requirements across Cellectis’ clinical programs. Knowledge and understanding of regulations regarding cell/gene therapies including but not limited to ICH guideline, GCP, and GMP as defined by the US Food and Drug Administration and European Medicines Agency.
NewNon-Clinical AxelonNon-ClinicalDurham, NC$1–$2 / hourSupports program build requirements by assisting in placing medical supplies into bins according to the 2-Bin system guidelines, labeling bins and carts accurately to ensure proper identification and inventory tracking and transporting supply carts to designated areas within the hospital system as needed. Key Responsibilities: Work with the 2-bin Team Lead in all aspects of the 2-bin project, including meeting with clinical clients, building cart hardware, maintaining and supporting hardware inventory, and following Team Lead requests as needed.
Senior Clinical Research Associate, Early Clinical Development IQVIASenior Clinical Research Associate, Early Clinical DevelopmentDurham, North CarolinaConduct all types of site visits—selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time).
Clinical Manager, Clinical Science, Cronos IQVIAClinical Manager, Clinical Science, CronosDurham, North CarolinaCronos combines deep clinical and scientific expertise with advanced clinical analytics, proprietary technology platforms and scalable global delivery models to support a broad range of therapeutic areas, partnering flexibly with sponsors, IQVIA CRO teams, and external CROs to reduce variability, prevent measurement risk, and enable more conclusive clinical research outcomes. Cronos is IQVIA’s global clinical outcome assessment and rater services business within the Patient‑Centered Solutions and Connected Technologies (PACT) business, providing scientifically rigorous rater training, certification, monitoring, and data quality oversight to improve endpoint reliability in clinical trials.
Global Clinical Operations Leader / Clinical Trial Manager Parexel International CorpGlobal Clinical Operations Leader / Clinical Trial ManagerRaleigh, NCRemoteWith more than 22,000 employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient focused clinical trials that broaden access and make research a care option for anyone anywhere. You will serve as the primary clinical liaison to project leadership and sponsor teams coordinating cross functional contributors across regions and time zones.
NewClinical Scientist/Senior Clinical Scientist, Cronos IQVIAClinical Scientist/Senior Clinical Scientist, CronosDurham, North CarolinaCronos combines deep clinical and scientific expertise with advanced clinical analytics, proprietary technology platforms and scalable global delivery models to support a broad range of therapeutic areas, partnering flexibly with sponsors, IQVIA CRO teams, and external CROs to reduce variability, prevent measurement risk, and enable more conclusive clinical research outcomes. Cronos is IQVIA’s global clinical outcome assessment and rater services business within the Patient‑Centered Solutions and Connected Technologies (PACT) business, providing scientifically rigorous rater training, certification, monitoring, and data quality oversight to improve endpoint reliability in clinical trials.
Clinical Assistant Professor or Clinical Associate Professor University of North Carolina at Chapel HillClinical Assistant Professor or Clinical Associate ProfessorChapel Hill, NCThe faculty member will have the primary responsibilities of: Teaching upper division undergraduate degree courses related to professional communication, leadership, research, medicolegal issues, and masters level research courses; Active role in leadership in the Division of Radiologic Science as specified with the Department Chair; Curriculum Director for master's degree program; Additional duties as assigned by Division Director or assumed role as Division Director. Department Health Sciences - Rad Sci - 405504 Posting Open Date 11/19/2025 Application Deadline Open Until Filled Yes Position Type Permanent Faculty Working Title Clinical Assistant Professor or Clinical Associate Professor Appointment Type Fixed Term Faculty Vacancy ID FAC0005738 Full-time/Part-time Full-Time Permanent Hours per week 40 FTE 1 Position Location North Carolina, US Hiring Range Dependent on Qualifications Proposed Start Date 05/01/2026.
Social/Clinical Research Specialist University of North Carolina at Chapel HillSocial/Clinical Research SpecialistChapel Hill, NC$62,000–$77,000 / yearDepartment Psychiatry - Research-412250 Career Area Research Professionals Posting Open Date 07/06/2026 Application Deadline 09/02/2026 Open Until Filled No Position Type Permanent Staff (EHRA NF) Working Title Social/Clinical Research Specialist Appointment Type EHRA Non-Faculty Position Number 20068826, 20068825 Vacancy ID NF0009862 Full Time/Part Time Full-Time Permanent FTE 1 Hours per week 40 Position Location North Carolina, US Hiring Range $62,000 - $77,000 Proposed Start Date 07/27/2026. The Senior Clinical Research Coordinator is responsible for the planning, organization, conduct, and evaluation of multi-faceted clinical research protocols, including study execution, developing strategies and solutions to improve study processes and execution, providing reviews of other team members' work product, and serving as mentor and subject matter expert.
NewSenior Clinical Project Manager (CAR-T) IQVIASenior Clinical Project Manager (CAR-T)Durham, North CarolinaYou'll work on some of the industry's most complex global clinical trials, partnering directly with leading pharmaceutical and biotechnology sponsors across therapeutic areas including Oncology, Rare Disease, CNS, Cardiovascular, Immunology, Respiratory, Cell & Gene Therapy, Infectious Disease, Ophthalmology and Women's Health. At IQVIA, you'll have the opportunity to work on high-profile global studies, collaborate with industry-leading sponsors, leverage cutting-edge technology and build a rewarding career with one of the world's leading clinical research organizations, all while helping bring innovative treatments to patients faster.
Per Diem Clinical Research Nurse - Home Visits Science 37 IncPer Diem Clinical Research Nurse - Home VisitsRaleigh, NC$50–$55 / hourWith 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.
Clinical Study Design Manager Science 37 IncClinical Study Design ManagerMorrisville, NCThe following qualifications are preferred and/or equivalent applicable experience: Required: 3+ years of experience in clinical research or life science industry, including at least 3 years in design of CRF/ePRO or other clinical trials database capture software. The Clinical Study Design Manager is responsible for working with our clients and internal staff to define the eSource platform specification design for the study, including all data capture requirements, bridging the gap between protocol requirements and implementation.
Clinical Research Associate 2, IQVIA IQVIAClinical Research Associate 2, IQVIADurham, North CarolinaEnsure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
RWE Clinical Project Manager (FSP) IQVIARWE Clinical Project Manager (FSP)Durham, North CarolinaIQVIA is hiring a clinical project manager to expand our dedicated Real World Evidence (RWE) FSP team, working fully within the environment of a prominent pharma company. In this role, the clinical project manager will be responsible for end-to-end project delivery of real-world observational studies within the oncology therapeutic area.
Manager, Clinical Operations IQVIAManager, Clinical OperationsDurham, North CarolinaManage a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced and employees are trained and meeting project objectives. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
Clinical Research Associate, Sponsor Dedicated IQVIAClinical Research Associate, Sponsor DedicatedDurham, North CarolinaEnsure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.