Clinical Decision Unit Clinical Nurse Coordinator Mission HospitalClinical Decision Unit Clinical Nurse CoordinatorAsheville, NCAdditional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-term care coverage, moving assistance, pet insurance and more. As a majority owner of Galen College of Nursing, which joins Research College of Nursing and Mercy School of Nursing as educational facilities within the HCA Healthcare family, we make it easier and more affordable to gain certifications and job skills.
Med-Surg Clinical Nurse Coordinator Mission HospitalMed-Surg Clinical Nurse CoordinatorMorganton, NCIn collaboration with other members of the management team, the CNC directs, monitors, and evaluates nursing care in accordance with established policies/procedures, serves as a resource person for staff, and models a commitment to the organization’s vision/mission/values to support an unparalleled patient experience and clinical outcomes that contribute to overall departmental performance. Additional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-term care coverage, moving assistance, pet insurance and more.
Licensed Clinical Social Worker (LeJeune) Choctaw GlobalLicensed Clinical Social Worker (LeJeune)Jacksonville, NC$90,000–$92,000 / yearAbility to obtain and maintain Secret OR Top Secret/SCI clearance .Current certification in Basic Life Support (BLS) issued by the American Red Cross or the American Heart Association Basic Life Support for Healthcare Providers. WHY JOIN CHOCTAW WORKFORCE SERVICES: Step into a role that goes beyond traditional clinical care – join a mission-driven team supporting the elite warriors of the United States Special Operations Command (USSOCOM).
NewRN Clinical Nurse II (Per Diem)- GI Surgery & Surgical Oncology Acute Care Unit UNC HealthRN Clinical Nurse II (Per Diem)- GI Surgery & Surgical Oncology Acute Care UnitChapel Hill, NC$33.88–$47.91 / hourOur patient populations require close post-operative observation, occasional remote cardiac telemetry, early aggressive mobilization, pulmonary hygiene, extensive physical therapies, IV, central line/PICC line care, administration of TPN, anticoagulation, oxygen therapy, pain management, blood product administration, intake/output and ostomy care. Our interdisciplinary team provides evidence-based and high-quality care primarily to adult post-surgical patients with weight loss issue, gastrointestinal (GI) cancers, and complex non-cancer GI-related illnesses.
RN Clinical Nurse II (Per Diem)- Trauma & Acute Care Surgery- 5 Bedtower UNC HealthRN Clinical Nurse II (Per Diem)- Trauma & Acute Care Surgery- 5 BedtowerChapel Hill, NC$34.22–$48.38 / hourInnovative Learning Opportunities in a Dynamic Work Environment: Ideal for new learners, our unit offers unique experiences and educational opportunities that foster professional growth and skill development. Consults with appropriate resources in a timely fashion regarding patients with complex care issues, unusual teaching needs and/or those at high risk for discharge planning.
NewData Coordinator ECLAROData CoordinatorChapel Hill, NC$28 / hourWorking closely with study coordinators, investigators, regulatory staff, sponsors, and clinical teams, the Data Coordinator helps maintain data integrity, support protocol compliance, and ensure high-quality research operations in accordance with Good Clinical Practice (GCP), federal regulations, sponsor requirements, and institutional policies. This position independently manages data-related activities for multiple studies throughout the clinical trial lifecycle, including startup, implementation, monitoring, and closeout.
Clinical Instructor/Clinical Assistant Professor/Clinical Associate Professor/Clinical Professor/Teaching Assistant Professor/Teaching Associate Professor/Teaching Professor/Research Assistant Professor/Research Associate Professor/Research Professor East Carolina UniversityClinical Instructor/Clinical Assistant Professor/Clinical Associate Professor/Clinical Professor/Teaching Assistant Professor/Teaching Associate Professor/Teaching Professor/Research Assistant Professor/Research Associate Professor/Research ProfessorGreenville, NCJob Title Clinical Instructor/Clinical Assistant Professor/Clinical Associate Professor/Clinical Professor/Teaching Assistant Professor/Teaching Associate Professor/Teaching Professor/Research Assistant Professor/Research Associate Professor/Research Professor Position Number MR-EM-2026-01 Vacancy Open to All Candidates Department EHH BSOM Emergency Medicine Department Homepage https://emergency-medicine.ecu.edu/ In the Department of Emergency Medicine, our mission is to provide and continue to improve the quality of health care services whenever and wherever the patient needs them; to promote scholarly activity regarding emergency health care through education and research; and to maximize the accumulation and utilization of resources in order to accomplish service and scholarly activities, and promote the wellness and satisfaction of department members.
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 Research Associate/Senior Clinical Research Associate- FSP ParexelClinical Research Associate/Senior Clinical Research Associate- FSPNorth CarolinaFollows quality issue processes by escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance issues to Local Management and/or Clinical Quality Management (CQM) as required. The CRA is responsible for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies, in compliance with Client Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies.
Senior Clinical Research Associate, Early Clinical Development IQVIA Holdings IncSenior Clinical Research Associate, Early Clinical DevelopmentDurham, NC$87,200–$169,300 / yearConduct 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).
In-house Clinical Research Associate II - CNS/Oncology Worldwide Clinical Trials Holdings IncIn-house Clinical Research Associate II - CNS/OncologyNC$50,000–$99,000 / yearThe In-House Clinical Research Associate II provides support to Clinical Trial Managers (CTM) and field Clinical Research Associates (CRA) and collaborates with project team members across a variety of roles and departments to ensure timely achievement of site management deliverables per contracted timelines. Provide visit preparation support for field CRAs, including but not limited to routine summation/communication of (e.g., Action Items, Protocol Deviations, EDC queries, vendor queries, study supplies, and/or pending site staff training prior to scheduled onsite visits, etc.).
In-house Clinical Research Associate II - CNS/Neurology Worldwide Clinical Trials Holdings IncIn-house Clinical Research Associate II - CNS/NeurologyNC$50,000–$99,000 / yearThe In-House Clinical Research Associate II provides support to Clinical Trial Managers (CTM) and field Clinical Research Associates (CRA) and collaborates with project team members across a variety of roles and departments to ensure timely achievement of site management deliverables per contracted timelines. Provide visit preparation support for field CRAs, including but not limited to routine summation/communication of (e.g., Action Items, Protocol Deviations, EDC queries, vendor queries, study supplies, and/or pending site staff training prior to scheduled onsite visits, etc.).
Senior Clinical Research Associate (level dependent on experience) CTISenior Clinical Research Associate (level dependent on experience)Raleigh, North CarolinaFor that reason, we treat our team members with the respect they deserve, and our numbers show it: We support career progression – We believe in promoting from within and we have a structured mentoring program and program for recent graduates to provide the support employees need to move forward. To help support the unique job functions of our CRAs, we have a dedicated training department that offers ongoing therapeutic training sessions from our world-class medical directors, and an experienced and supportive management team that is there to offer continual guidance.
Clinical Research Associate (CRA) Zp Group LlcClinical Research Associate (CRA)RALEIGH, NC$100,000–$130,000 / yearYou will work closely with investigators, site personnel, and study teams to support the delivery of high-quality clinical research and contribute to the advancement of groundbreaking oncology therapies. Zachary Piper Solutions is seeking a talented REMOTE Clinical Research Associate (CRA) to support a leading clinical research organization advancing innovative oncology studies.
FSP 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.
FSP 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.
FSP Clinical Research Associate 2 - California or Colorado Fortrea IncFSP Clinical Research Associate 2 - California or ColoradoDurham, 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.
FSP Sr. Clinical Research Associate II - NYC Metro or PHL - Onc Fortrea IncFSP Sr. Clinical Research Associate II - NYC Metro or PHL - OncDurham, NCRemote$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 - West Region Fortrea IncFSP Clinical Research Associate 2 - West 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.
Clinical Research Associate III Connexion Systems + EngineeringClinical Research Associate IIIDurham, NCThis position is ideal for an experienced oncology CRA with direct early-phase (Phase I) monitoring experience who enjoys working collaboratively across cross-functional teams while serving as the primary sponsor representative for assigned study sites. Our client is seeking an experienced Clinical Research Associate III to join its Clinical Operations team supporting Phase I oncology clinical trials .