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).
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.
Clinical Research Associate II - Oncology - United States (Remote) Worldwide Clinical TrialsClinical Research Associate II - Oncology - United States (Remote)Durham, NCRemote$79,500–$158,500 / yearWe are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way. As a CRA II, you will play a critical role in ensuring the successful execution of clinical trials by: Performing on-site and remote monitoring visits in accordance with protocol, GCP, ICH guidelines, and company SOPs.
Clinical Research Associate II - Psychiatry - United States (Remote) Worldwide Clinical TrialsClinical Research Associate II - Psychiatry - United States (Remote)Durham, NCRemote$79,500–$158,500 / yearWe are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way. As a CRA II, you will play a critical role in ensuring the successful execution of clinical trials by: Performing on-site and remote monitoring visits in accordance with protocol, GCP, ICH guidelines, and company SOPs.
Clinical Research Coordinator Duke UniversityClinical Research CoordinatorDurham, NC$59,829–$99,960 / yearThis CRP will perform EMR review, participant screening, travelling for screening events as needed, consenting, enrollment, recruitment and retention, conducting study visits in the healthcare setting as well as in the community, management of specimens, study and site documentation, data collection and entry, query resolution, interventional- drug/device studies, IP management, IRB/regulatory submissions and maintenance, and participant payment processing. Composed of more than 2,500 faculty physicians and researchers, more than 1,300 students, and more than 6,000 staff, the Duke University School of Medicine along with the Duke University School of Nursing, Duke University Health System and the Private Diagnostic Clinic (PDC) comprise Duke Health.
Director, Clinical Research Scientist IREDirector, Clinical Research ScientistRaleigh, North Carolinamanagement, Project Teams, Joint Project Teams and/or Steering Committees (if appropriate), Clinical sub-teams, internal strategy, and governance meetings, eDMC meetings, steering committees, advocacy groups, scientific advisory boards, and publications committees. Will lead the clinical matrix teams for assigned studies, represent clinical development on project teams and serve as liaison to project teams, CRO's and others.
Associate Director, Strategy & Insights- Clinical Research Group Thermo Fisher ScientificAssociate Director, Strategy & Insights- Clinical Research GroupMorrisville, North CarolinaRemoteIn this prominent position, you’ll serve as a trusted expert and visionary leader, crafting bold, patient-centric recruitment and engagement strategies that empower individuals, support diverse communities, and accelerate our clients’ research and drug development goals. Serve as a trusted strategic advisor and subject matter expert for clients and internal stakeholders—guiding best practices, influencing direction, and helping teams adopt a patient-first mindset.
Sr Clinical Research Associate VeranexSr Clinical Research AssociateRaleigh, NCRemoteGenerates high-quality site qualification, initiation, monitoring, and close-out visit reports in timely manner (in accordance with the Clinical Monitoring Plan)Contributes to protocol, informed consent, case report form (CRF) and study plan development as well as annual progress reports (APRs) and the clinical study report (CSR) at study conclusion to report the study results to FDA and other regulatory authorities. Conducts site qualification visits, study start-up activities (essential document collection), site qualification visits, site initiation visits and training, monitoring visits for source data verification (reported study data are accurate, complete, and verifiable from source documents in the site's medical records), and site close-out visits.
Lead Procurement Analyst, Category Management (Clinical Research) United Therapeutics CorporationLead Procurement Analyst, Category Management (Clinical Research)Raleigh, NCAs Lead Procurement Analyst, Category Management, you'll support clinical research by partnering with internal teams (Clinical Operations, Medical Affairs, etc.) to understand what they need, connect them with the right suppliers, and help make sure services and services are in place when they're needed. This is a role for someone who can balance business needs, supplier relationships, compliance, and cost awareness while keeping the bigger purpose in mind: helping execute the research that can bring new therapies and technologies closer to patients.
Associate Principal, Patient-Centered Research IQVIAAssociate Principal, Patient-Centered ResearchDurham, North CarolinaThis research includes qualitative (e.g., patient interviews, focus groups), quantitative (e.g., clinical outcome assessments (COAs)/patient-reported outcomes (PROs), preference research) and passive (e.g., digital health technology tools) approaches to understand patient, caregiver and physician experiences and expectations of disease and treatment. Strong experience working in roles generating or communicating robust clinical data suitable for submission to regulatory bodies, payers or for publication; preferably with exposure to COA/PRO, patient preference and/or HEOR.
NewPostdoctoral Research Associate University of North Carolina at Chapel HillPostdoctoral Research AssociateChapel Hill, NCDepartment SOP-DPMP - 452400 Posting Open Date 08/13/2026 Application Deadline 08/27/2026 Open Until Filled No Position Type Postdoctoral Scholar Position Title Postdoctoral Research Associate Vacancy ID PDS004942 Full-time/Part-time Full-Time Temporary Hours per week 40 FTE 1 Work Location Chapel Hill, NC Position Location North Carolina, US Hiring Range $60,000.00 Proposed Start Date Estimated Duration of Appointment 12 Months. A global higher education leader in innovative teaching, research and public service, the University of North Carolina at Chapel Hill consistently ranks as one of the nation's top public universities and is among is the top ten research universities in the nation for federal research expenditures as well as for federally funded social and behavioral sciences research and development.
NewFSP Clinical Research Associate 2 - OH, PA, VA Fortrea IncFSP Clinical Research Associate 2 - OH, PA, VADurham, NCRemote$100,000–$112,000 / yearResponsibilities: Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.
NewFSP Clinical Research Associate 2 - Central Region Fortrea IncFSP Clinical Research Associate 2 - Central RegionDurham, NCRemote$100,000–$112,000 / yearResponsibilities: Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.
Senior Clinical Research Associate ProPharma GroupSenior Clinical Research AssociateRaleigh, North CarolinaCommunicate with assigned clinical sites, investigators, site personnel, client personnel, and any other cross functional team member involved in the assigned clinical trials to address any study needs related to the monitoring and site management activities as assigned. Monitor assigned clinical trials and clinical sites by reviewing and reporting site enrollment, and termination updates, monitoring visits, protocol deviations, serious adverse events, laboratory abnormalities and any other activity at the site that contributes to proper conduct of the clinical trial per protocol, and regulatory requirements.
Principal, Patient-Centered Research IQVIAPrincipal, Patient-Centered ResearchDurham, North CarolinaSuccess will be measured by the ability to take on larger and more complex projects, establishing new business relationships, coaching and professionally developing team members, and contributing to the continuous improvement and development of the PCS function. Our diverse team of experts works together to develop, deploy, and validate psychometric instruments that capture the patient experience with their treatment or disease, analyze and interpret outcomes, and translate the information to advance the initiatives of life science companies.
FSP Sr. Clinical Research Associate II - NYC Metro or PHL - Onc FortreaFSP Sr. Clinical Research Associate II - NYC Metro or PHL - OncDurham, North CarolinaRemote$125,000–$140,000 / yearResponsibilities : Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.
FSP Sr. Clinical Research Associate II - Denver, CO - Oncology FortreaFSP Sr. Clinical Research Associate II - Denver, CO - OncologyDurham, North CarolinaRemote$125,000–$140,000 / yearResponsibilities : Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.
FSP Clinical Research Associate 2 - California or Colorado FortreaFSP Clinical Research Associate 2 - California or ColoradoDurham, North CarolinaRemote$100,000–$112,000 / yearResponsibilities : Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.
NewFSP Clinical Research Associate 2 - OH, PA, VA FortreaFSP Clinical Research Associate 2 - OH, PA, VADurham, North CarolinaRemote$100,000–$112,000 / yearResponsibilities : Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.
NewFSP Clinical Research Associate 2 - Central Region FortreaFSP Clinical Research Associate 2 - Central RegionDurham, North CarolinaRemote$100,000–$112,000 / yearResponsibilities : Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.