Senior Clinical Project Manager Azurity PharmaceuticalsSenior 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.
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.
Senior Clinical Project Manager, Phase I Fortrea IncSenior Clinical Project Manager, Phase IDurham, NCRemote$140,000–$150,000 / yearTEAM COMMUNICATION: Serve as key client contact for assigned projects, establishing working relationships with client project teams which result in client satisfaction, operational excellence and thereby increase potential for repeat business. Responsibilities typically include developing and managing project teams, communications, risk, scope, schedule, cost, quality, and stakeholders, effectively ensuring that variance from plan is proactively and effectively mitigated and client expectations are met.
Executive Director, Clinical Platforms & Product Development FortreaExecutive Director, Clinical Platforms & Product DevelopmentDurham, North CarolinaRemoteThe Executive Director leads the operating engine for Clinical Platforms, ensuring predictable delivery, strong governance, and high-quality execution across internal teams, external vendors, and client-facing activities. This position is accountable for the full lifecycle of clinical technology solutions—from concept and product strategy through engineering, deployment, and operational enablement—ensuring alignment with Fortrea’s clinical trial delivery model, regulatory environment, and sponsor expectations.
Senior Clinical Research Associate ICON PlcSenior Clinical Research AssociateRaleigh, NCRemoteICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
FSP - Clinical Team Lead - Ophthalmology - US & Canada FortreaFSP - Clinical Team Lead - Ophthalmology - US & CanadaDurham, North CarolinaLead the development of the clinical project strategy and ensures prioritization with the clinical project team and key stakeholders in the creation of clear, data driven strategies and proactive management of project scope, timelines, quality and budget. Demonstrated ability to lead by example and to encourage team members to seek solutions independently Demonstrated ability to handle multiple competing priorities and to utilize resources effectively.
Clinical Team Lead, FSP - Oncology - US & Canada FortreaClinical Team Lead, FSP - Oncology - US & CanadaDurham, North CarolinaLead the development of the clinical project strategy and ensures prioritization with the clinical project team and key stakeholders in the creation of clear, data driven strategies and proactive management of project scope, timelines, quality and budget. Demonstrated ability to lead by example and to encourage team members to seek solutions independently Demonstrated ability to handle multiple competing priorities and to utilize resources effectively.
Senior Clinical Project Manager, Immuno-Oncology, IQVIA Biotech IQVIA Holdings IncSenior Clinical Project Manager, Immuno-Oncology, IQVIA BiotechDurham, NC$93,100–$232,800 / yearAs a Senior Project Manager at IQVIA Biotech, you'll play a critical role in accelerating the delivery of clinical trials and improving patient lives by bringing new therapies to market faster. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
Vice President, Clinical Development Grifols SAVice President, Clinical DevelopmentNCWith responsibility across a diverse therapeutic portfolio and modalities - including plasma-derived products and recombinant proteins - this role offers a rare opportunity to build future-ready development capabilities, influence portfolio strategy, and lead teams that translate deep biological insight into medicines that meaningfully improve patients' lives. Author and deliver high-quality clinical regulatory documents: Lead the planning, writing, and review of key documents including clinical study reports (CSRs), protocols, investigator brochures, briefing packages, and regulatory submissions, ensuring clarity, scientific rigor, and compliance with ICH/GCP and regulatory guidelines.
Clinical Trial Manager - CAR T or Ophthalmology FortreaClinical Trial Manager - CAR T or OphthalmologyDurham, North CarolinaProactively identify and address start-up and clinical project, financial, and quality risks by applying comprehensive risk management strategies and ensuring compliance, including tracking within applicable systems. This role collaborates with project managers and other functional leads to deliver clinical and start-up activities within budget and contract, ensuring quality, compliance and meeting country-specific commitments.
Senior Clinical Project Manager, Phase I FortreaSenior Clinical Project Manager, Phase IDurham, North CarolinaRemoteTEAM COMMUNICATION: Serve as key client contact for assigned projects, establishing working relationships with client project teams which result in client satisfaction, operational excellence and thereby increase potential for repeat business. Responsibilities typically include developing and managing project teams, communications, risk, scope, schedule, cost, quality, and stakeholders, effectively ensuring that variance from plan is proactively and effectively mitigated and client expectations are met.
Clinical Studies Registered Nurse II, Cardiology Advocate Health and Hospitals CorporationClinical Studies Registered Nurse II, CardiologyWake Forest, North CarolinaPromotes communication and collaborative activities between Radiation, Gynecological, Surgical and Medical Oncology staff, special laboratory staff, research personnel and investigators for multi-disciplinary (multimodality) research studies to ensure quality patient care, efficient and effective operation of protocol processes, and achievement of study-related objectives. Serves as an advocate for human subjects by establishing and maintaining communication with Investigators, research staff, Sponsors, participants and representatives of professional organizations, participant advocates, and public responsible for, or concerned about, protections for human participants of research.
Clinical Support Technician - University of North Carolina at Chapel Hill UNC HealthClinical Support Technician - University of North Carolina at Chapel HillChapel Hill, NCDepartmentTraCS Institute - 429801Career AreaHealth Professional (Physician/Nurse/Other)Posting Open Date08/14/2026Application Deadline09/07/2026Position TypeTemporary Staff (SHRA)Position TitleClinical Support TechnicianPosition Number20078107Vacancy IDS027967Full-time/Part-timeFull-Time TemporaryHours per week40Work Schedule. University employees can choose from a wide range of professional training opportunities for career growth, skill development and lifelong learning and enjoy exclusive perks that include numerous retail and restaurant discounts, savings on local child care centers and special rates for performing arts events.
Supervisor Clinical Nurse IV- Staffing Response Team Night Shift UNC HealthSupervisor Clinical Nurse IV- Staffing Response Team Night ShiftRaleigh, NC$38.51–$58.82 / hourThe Supervisor Clinical Nurse IV - Central Staffing Office is a senior nursing leader responsible for coordinating and supervising centralized staffing operations to support safe, high‑quality patient care across UNC Health Rex. Support daily operations of the Central Staffing Office, including: Coordination and deployment of nursing and support staff to inpatient areas and Emergency Departments at both UNC Rex Raleigh and UNC Rex Holly Springs.
Executive Assistant, Legal Velocity Clinical Research, Inc.Executive Assistant, LegalDurham, North CarolinaFull timeAdvanced proficiency in Microsoft Office and collaboration tools, including Word, Excel, PowerPoint, Outlook, Teams, SharePoint, Adobe Acrobat Pro, and document management systems; experience with project management tools preferred. The Executive Assistant serves as a trusted partner to the General Counsel, enabling efficient management of legal operations, communications, documentation, compliance initiatives, and departmental workflows.
Clinical Care Advisor IDD (Program Consultant) Elevance Health IncClinical Care Advisor IDD (Program Consultant)Durham, NCHow you will make an impact: In collaboration under the supervision of the Manager II this candidate will manage the ongoing compliance; daily operations with external client facing programs; helps ensure program meets its stated objectives; provides support to a team of advisors in day to day operations. Minimum Requirements: Requires a BA/BS in a related field and minimum of 3 years experience in external client facing program management; or any combination of education and experience, which would provide an equivalent background.
Executive Director, Clinical Development & Medical Affairs Humacyte IncExecutive Director, Clinical Development & Medical AffairsDurham, NCCOMPANY: Humacyte Inc (Nasdaq: HUMA) is developing a disruptive biotechnology platform to deliver universally implantable bioengineered human tissues, advanced tissue constructs, and organ systems designed to improve the lives of patients and transform the practice of medicine. Humacyte's initial opportunity, a portfolio of Acellular Tissue Engineered Vessel (ATEVs), is currently approved for use in vascular trauma repair and is in late-stage clinical trials targeting multiple other applications including AV access for hemodialysis and peripheral arterial disease.
Senior Clinical Project Manager- CNS IQVIA Holdings IncSenior Clinical Project Manager- CNSDurham, NC$93,100–$232,800 / yearBuild the cross-functional project team and lead their efforts, responsible for managing cross-collaboration of the core team and for overall project delivery to support milestone achievement and to manage study issues and obstacles. The Senior Project Lead is an essential member of the core project team leading the team and responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices.
Active_Clinical Research Coordinator 3 eTeam Inc.Active_Clinical Research Coordinator 3Durham, NC$38.87 / hourProvide clinical research support to investigators to prepare for and execute assigned research studies, including: Review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data. Collect, record, and maintain research subject study data according to study protocol and SOPs, preserving quality control for content, accuracy, and completeness.
Associate Clinical Lead Director IQVIA Holdings IncAssociate Clinical Lead DirectorDurham, NC$102,500–$285,500 / yearKnowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) and relevant local laws, regulations and guidelines, towards clinical trial conduct. Associate Clinical Lead Directors ensure clinical delivery to customers, lead clinical teams and partner with Project Leaders and other functional teams to ensure projects meet delivery requirements.