NewHOME CARE CLINICAL MANAGER - RN Liberty HealthHOME CARE CLINICAL MANAGER - RNFayetteville, NCProvide direct patient care as necessary to include case management, Oasis care planning, assigning Care staff, and ensuring the efficient, effective utilization of existing staffing resources. Ability to independently organize work, provide appropriate case management, cost-effective home healthcare services, and timely, accurate documentation of said care.
General Dentistry Faculty - Community Service Learning Center, Clinical Assistant Professor, Clinical Associate Professor, Clinical Professor East Carolina UniversityGeneral Dentistry Faculty - Community Service Learning Center, Clinical Assistant Professor, Clinical Associate Professor, Clinical ProfessorLumberton, NCAdvertising Department DENTAL MEDICINE, SCHOOL OF Division Academic Affairs Classification Title General Dentistry Faculty - Community Service Learning Center, Clinical Assistant Professor, Clinical Associate Professor, Clinical Professor Working Title General Dentistry Faculty - Community Service Learning Center, Clinical Assistant Professor, Clinical Associate Professor, Clinical Professor Number of Vacancies 1 Full Time Equivalent (FTE) 1.00 Full Time or Part Time Full Time Anticipated Recruitment Range. The Administrative units include the Offices of the Dean, Vice Dean, Associate Dean for Student Affairs, Associate Dean for Research, Associate Dean for Clinical Affairs, Associate Dean for Extramural Clinical Practices, Assistant Dean for Dental Education and Informatics, Assistant Dean for Educational Support and Faculty Development, Assistant Dean for Academic Success, and the Assistant Dean for Business Operations and Financial Affairs.
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.
Assistant Professor in Clinical Mental Health Counseling/Clinical Placement Coordinator Methodist UniversityAssistant Professor in Clinical Mental Health Counseling/Clinical Placement CoordinatorFayetteville, NCServe as liaison with students, other educators, staff, and outside community agencies and partners in facilitating program objectives, including but not limited to developing, and facilitating residency workshops, coordinating logistics, site vetting, site supervision, training and other student activities and duties. For full consideration, qualified applicants should submit the following: 1) letter of intent; 2) curriculum vitae; teaching and supervision philosophy statements; 4) concise statement about your approach to teaching or other initiatives designed to foster a sense of student engagement, community, and belonging; 5) transcripts; and 6) contact information for three references.
Clinical Research Coordinator II Care AccessClinical Research Coordinator IIFayetteville, North Carolina$60,000–$90,000 / yearWith programs like Future of Medicine , which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers , which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. The Clinical Research Coordinator ’s primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.
Manager, Site Contracts with Clinical Trials experience Hybrid or Remote in USA-NC Syneos HealthManager, Site Contracts with Clinical Trials experience Hybrid or Remote in USA-NCNorth CarolinaRemoteBachelor’s degree in life sciences, nursing degree, or equivalent related experience, plus extensive clinical research experience in a contract research organization, pharmaceutical or Biotechnology Company, including some time in a leadership capacity or equivalent combination of education, training and experience is required. Participates in managing the resource availability for their team members to ensure they are suitably resourced and resource needs are identified in a timely fashion; resolves potential resourcing conflicts to facilitate mutually beneficial resolutions.
Clinical Research Coordinator Odyssey Systems Consulting Group, Ltd.Clinical Research CoordinatorFort Bragg, North CarolinaFull timePosition Summary: Odyssey is looking for a Clinical Research Coordinator to coordinate and assure the integrity of all activities associated with conducting Traumatic Brain Injury Center of Excellence (TBICoE) clinical investigations in TBI, brain health, and related outcomes. Prepares requests for actions/proposals to include assisting with and providing coordination for grant proposal applications and their associated documentations and requirements as Facilitates the flow and approval processes for relevant projects as needed or requested.
Clinical Project Manager - Oncology (Client Dedicated/Remote) Syneos HealthClinical Project Manager - Oncology (Client Dedicated/Remote)North CarolinaRemoteWe are seeking experienced Clinical Project Managers with strong global oncology clinical trial experience to join a high-performing sponsor-dedicated team supporting a diverse portfolio of oncology studies across multiple indications and phases of development. We are specifically seeking professionals with 3+ years of hands-on Clinical Project Management experience leading global oncology studies and collaborating with cross-functional teams, vendors, and international stakeholders.
Experienced Clinical Project Manager – Cell & Gene Therapy (Sponsor Dedicated/ Remote: US only) Syneos HealthExperienced Clinical Project Manager – Cell & Gene Therapy (Sponsor Dedicated/ Remote: US only)North CarolinaRemoteWe are seeking a skilled and motivated Project Manager I to join our sponsor-dedicated team supporting high-impact oncology and cell & gene therapy trials, including CAR-T studies. Experienced Clinical Project Manager – Cell & Gene Therapy (Sponsor Dedicated/ Remote: US only) Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.
Clinical Trial Manager - Full Service Syneos HealthClinical Trial Manager - Full ServiceNorth CarolinaClinical Trial Management System (CTMS), Electronic Data Capture (EDC), eDiary, Electronic Patient Reported Outcomes (ePROs), Trial Master File (TMF), IVRS/IWRS, Central Monitoring dashboards), to oversee site and patient activities, study team conduct and to ensure the data has been updated to reflect timely execution of all operational aspects (required visits/calls, duration, and frequency) according to plan. Reviews the content and quality of site and central monitoring documentation (site monitoring calls, site visit reports, site letters, central monitoring reports and pertinent correspondence), to ensure they represent site management activities and conduct and that they appropriately convey any risks to protocol/GCP compliance, trial conduct, patient safety or data integrity.
NewDirector, Clinical Development Sciences BioCryst PharmaceuticalsDirector, Clinical Development SciencesNorth CarolinaServes as subject matter expert for assigned clinical development program(s) and works closely with relevant stakeholders to lead development and implementation of trials and programs, including trial/program design, trial/program-specific data collection tools, data review tasks, and data analysis to ensure quality and consistency across the program. Is a primary member of the clinical development study team responsible for optimal study execution and collection of data together with clinical operations, data management and statistics, accomplished through training CRAs, selection of laboratory assessments for safety and pharmacodynamics, and providing input into tables, listings and figures to be generated.
Clinical Research Coordinator II- Murtha Cancer Center The Henry M Jackson Foundation for the Advancement of Military Medicine IncClinical Research Coordinator II- Murtha Cancer CenterFort Bragg, NCHJF is seeking a Clinical Research Coordinator II to perform clinical research and patient treatment in conjunction with one or more specified clinical research protocols at Womack Army Medical Center (WAMC) at Fort Bragg, North Carolina. Its comprehensive core of military and civilian oncologists and other cancer-trained clinicians and researchers provide multidisciplinary cancer-care delivery and patient-family support services.
Principal Research Scientist ONC -Clinical Development Scientist (Sponsor Dedicated/ Remote US) Syneos HealthPrincipal Research Scientist ONC -Clinical Development Scientist (Sponsor Dedicated/ Remote US)North CarolinaRemoteWe are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. Principal Research Scientist ONC -Clinical Development Scientist (Sponsor Dedicated/ Remote US) Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success.
Clinical Client Success Manager MPOWERHealthClinical Client Success ManagerNorth CarolinaFull timeThe Clinical Client Success Manager is responsible for routinely managing client accounts, proactively communicating with all clients, and providing day-to-day management and operational support of clinical services. · Perform regular calls or face-to-face meetings with assigned clients to review reporting, additional training needs, project status, review outstanding issues and any new opportunities to integrate additional services.
NewClinical Scientist - FSP ParexelClinical Scientist - FSPNorth CarolinaThe Clinical Scientist (CS) assists the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies (e.g., adjudication support, medical monitoring, imaging data reconciliation preparation of meeting materials, protocol deviation management). From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
NewClinical Research Coordinator II - Murtha Cancer Center (Prometheus 31B) The Henry M Jackson Foundation for the Advancement of Military Medicine IncClinical Research Coordinator II - Murtha Cancer Center (Prometheus 31B)Fort Bragg, NCThe study entitled "Capillary Blood Collection Study for Service Members Stationed at Fort Bragg" seeks to demonstrate the feasibility and utility of "dried blood spot" technology as a sampling and biorepository mechanism. The incumbent will coordinate all research activities related to the performance and compliance of all research projects in multidisciplinary areas under the directions of designated Principal Investigators and the leadership of Murtha Cancer Center at Walter Reed Bethesda.
Experienced Clinical Research Associate - Sponsor Dedicated Syneos HealthExperienced Clinical Research Associate - Sponsor DedicatedNorth CarolinaPerforms site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan.
Clinical Research Associate - Full-Service Syneos HealthClinical Research Associate - Full-ServiceNorth CarolinaPerforms site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan.
Clinical Research Coordinator II Care Access Research LLCClinical Research Coordinator IIFayetteville, NC$60,000–$90,000 / yearWith programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. The Clinical Research Coordinator's primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.
Biotech Project Leadership - Clinical Trials - Home- Based - (Future Needs) ParexelBiotech Project Leadership - Clinical Trials - Home- Based - (Future Needs)North CarolinaSuccessful candidates possess an undergraduate degree in a clinical or health related field: advanced degree preferred, along with at minimum, 2+ years' experience leading Global Clinal Trials in Project Management within a CRO (preferred), Biotech or Pharma company. Parexel has upcoming opportunities at the Project Leader (PM) and Senior Project Leader (SPM) level for candidates with experience leading global studies in a variety of therapeutics including Neurology, Oncology (Hematology), Respiratory, Cardio, General Medicine and GLP-1 /Obesity.