NewHOSPICE CLINICAL MANAGER - RN Liberty HealthHOSPICE CLINICAL MANAGER - RNDunn, 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.
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 ProfessorNCThe 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. The General Dentistry Faculty at a Community Service Learning Center (CSLC) of the School of Dental Medicine, East Carolina University, is a full-time faculty member who will provide leadership and supervision of educational and clinical activities in the Community Service Learning Center (CSLC) while providing a full range of general dentistry services in an underserved community.
Clinical Research Associate/Senior Clinical Research Associate- FSP Parexel International CorpClinical Research Associate/Senior Clinical Research Associate- FSPNCFollows 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 works in close collaboration with other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study commitments are achieved in a timely and efficient manner.
Senior Clinical Research Associate/Clinical Research Associate - All US Locations - FSP Parexel International CorpSenior Clinical Research Associate/Clinical Research Associate - All US Locations - FSPNCFollows 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/Clinical Research Associate - All US Locations - FSP ParexelSenior Clinical Research Associate/Clinical Research Associate - All US Locations - 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.
Director, Project Management - (Clinical Trials) - Oncology - Home Based Parexel International CorpDirector, Project Management - (Clinical Trials) - Oncology - Home BasedNCSuccessful candidates will have a minimum of an undergraduate degree in a science or health related field, (advanced degree preferred); minimum of 10 -15 years clinical research experience preferred with at least 10 years Project Management experience with a focus leading domestic and international oncology studies across phases. Reporting to the SVP, Head of Biotech Project Leadership Americas, this Home-Based position requires a seasoned professional with extensive experience at the Director level, overseeing both client management and deliverables of clinical trials as well as providing line management and individual team member development.
Clinical Sr Project Manager / Assoc Director (Global role, Multisponsor) ** Remote US & Canada ** Syneos HealthClinical Sr Project Manager / Assoc Director (Global role, Multisponsor) ** Remote US & Canada **North CarolinaRemoteThe position provides customer focused leadership in managing and delivering the operational and financial aspects of one or more clinical projects from proposal development to final deliverables and ranging in size and complexity from single service studies to full scope, multiple protocol projects and/or global projects across various phases and functional areas with limited interaction from supervisor. Directs the activities of assigned Project Support staff; line manages and mentors other project management team members and clinical staff; facilitates team building and communication.
NewSenior Clinical Research Associate - Rare CNS - Southeast/Mid-Atlantic (Remote) Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - Rare CNS - Southeast/Mid-Atlantic (Remote)NCRemote$97,000–$193,000 / yearTypically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.
Senior Clinical Research Associate - Cardio - East Coast - Remote Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - Cardio - East Coast - RemoteNCRemote$97,000–$193,000 / yearTypically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.
Senior Clinical Research Associate - Rare Disease - East Coast/Central (Remote) Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - Rare Disease - East Coast/Central (Remote)NCRemote$97,000–$193,000 / yearTypically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.
Regional Travel, Clinical Research Coordinator Care AccessRegional Travel, Clinical Research CoordinatorFayetteville, NCRemote$75,000–$105,000 / 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.
Clinical Research Associate II - North Carolina, East Coast Perspective Therapeutics IncClinical Research Associate II - North Carolina, East CoastNCClinical Trial Monitoring: Conduct site qualification, site initiation, interim monitoring, and close-out visits to ensure compliance with the study protocol, Good Clinical Practice (GCP), and regulatory guidelines. As a Clinical Research Associate II (CRA II) specializing in oncology, you will play a crucial role in the execution and management of Phase 1, Phase 2, and Phase 3 clinical trials.
NewSenior Clinical Trial Manager - Oncology - U.S. (Remote) Worldwide Clinical Trials Holdings IncSenior Clinical Trial Manager - Oncology - U.S. (Remote)NCRemote$112,000–$222,000 / yearClinical Trial Managers (CTMs) and Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve. We 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.
Regional Travel, Clinical Research Coordinator Care Access Research LLCRegional Travel, Clinical Research CoordinatorFayetteville, NCRemote$75,000–$105,000 / 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.
Clinical Project Manager (US) AlimentivClinical Project Manager (US)Raleigh-Durham, North CarolinaAct as primary liaison throughout the project life cycle ensuring client/sponsor expectations are appropriately managed by addressing and resolving queries/issues, planning and executing all project meetings, assisting with site and patient recruitment strategies and materials, assisting with the development of stakeholder training and by regularly providing sponsor/client with project status and update reports. Identify, assign and monitor the completion of interdisciplinary project tasks that include site monitoring, CRF and database development and revision, data collection, patient safety/adverse event management, document management, statistical analysis and/or final report writing and publications.
Director, Project Management - (Clinical Trials) - Oncology - Home Based ParexelDirector, Project Management - (Clinical Trials) - Oncology - Home BasedNorth CarolinaSuccessful candidates will have a minimum of an undergraduate degree in a science or health related field, (advanced degree preferred); minimum of 10 -15 years clinical research experience preferred with at least 10 years Project Management experience with a focus leading domestic and international oncology studies across phases. Reporting to the SVP, Head of Biotech Project Leadership Americas, this Home-Based position requires a seasoned professional with extensive experience at the Director level, overseeing both client management and deliverables of clinical trials as well as providing line management and individual team member development.
Project Leadership - Biotech (clinical trials) - Oncology - Home Based - (Future Needs) Parexel International CorpProject Leadership - Biotech (clinical trials) - Oncology - Home Based - (Future Needs)NCSuccessful 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. Individuals selected for these roles will provide leadership to project teams and manage the day-to-day operations while striving to achieve operational excellence through on time delivery within budget and to the highest quality with the goal to exceed client expectations.
Project Leadership - Biotech (clinical trials) -Neurology/Psych/Rare Disease - Home Based - (Future Needs) Parexel International CorpProject Leadership - Biotech (clinical trials) -Neurology/Psych/Rare Disease - Home Based - (Future Needs)NCSuccessful 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. Individuals selected for these roles will provide leadership to project teams and manage the day-to-day operations while striving to achieve operational excellence through on time delivery within budget and to the highest quality with the goal to exceed client expectations.
Project Leadership - Mid/Large- (clinical trials) - Homebased - (future needs) Parexel International CorpProject Leadership - Mid/Large- (clinical trials) - Homebased - (future needs)NCThe Global Project Leadership department has dedicated members at all levels who are aligned to work with specific types of clients and deliver solutions customized to fit those client's needs, working on projects spanning across all phases of global clinical trials, in a wide array of therapeutic areas. Parexel has upcoming opportunities in a variety of therapeutics at the Project Leader (PM) and Senior Project Leader (SPM) level for candidates with experience leading global studies in a variety of therapeutics supporting mid to large size biotech/ pharma clients.
Project Leadership - Biotech (Clinical Trials) - GLP-1 / Obesity - Home Based Parexel International CorpProject Leadership - Biotech (Clinical Trials) - GLP-1 / Obesity - Home BasedNCSuccessful candidates possess an undergraduate degree in a clinical or health related field: advanced degree preferred, along with at minimum, 2+ years experience leading Global Clinical Trials in Project Management within a CRO (preferred), Biotech or Pharma company. Individuals selected for these roles will provide leadership to project teams and manage the day-to-day operations while striving to achieve operational excellence through on time delivery within budget and to the highest quality with the goal to exceed client expectations.
Biotech Project Leadership - Clinical Trials - Home- Based - (Future Needs) Parexel International CorpBiotech Project Leadership - Clinical Trials - Home- Based - (Future Needs)NCParexel has upcoming future 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. Successful 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.
Project Leadership - Biotech (clinical trials) -Dermatology - Home Based - (Future Needs) Parexel International CorpProject Leadership - Biotech (clinical trials) -Dermatology - Home Based - (Future Needs)NCSuccessful 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. Individuals selected for these roles will provide leadership to project teams and manage the day-to-day operations while striving to achieve operational excellence through on time delivery within budget and to the highest quality with the goal to exceed client expectations.
Project Leadership - Biotech (clinical trials) -Respiratory - Home Based - (Future Needs) Parexel International CorpProject Leadership - Biotech (clinical trials) -Respiratory - Home Based - (Future Needs)NCSuccessful candidates possess an undergraduate degree in a clinical or health related field: advanced degree preferred, along with at minimum, 2+ years experience leading Global Clinical Trials in Project Management within a CRO (preferred), Biotech or Pharma company. Individuals selected for these roles will provide leadership to project teams and manage the day-to-day operations while striving to achieve operational excellence through on time delivery within budget and to the highest quality with the goal to exceed client expectations.
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.
Experienced Clinical Trial Manager - Full-Service Syneos HealthExperienced Clinical 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.
Site Contracts Specialist with Clinical Trials experience Home-Based in US Syneos HealthSite Contracts Specialist with Clinical Trials experience Home-Based in USNorth CarolinaSite Contracts Specialist with Clinical Trials experience Home-Based in US Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. Support in generating amended contract and/or budget documents as necessary, preparing contract management documentation for projects, and streamlining the contract/proposal or internal processes; and initiates and introduces creative ideas and solutions.
Regulatory Affairs Consultant - Clinical Regulatory Affairs Parexel International CorpRegulatory Affairs Consultant - Clinical Regulatory AffairsNCThis highly visible role combines regulatory strategy, global project leadership, health authority engagement, and cross-functional collaboration across programs ranging from early clinical development through registration planning and lifecycle management. Manage and support regulatory submissions and maintenance activities, including IND applications, annual reports, safety submissions, CTA-related activities, protocol amendments, informed consent updates, and end-of-trial deliverables.
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.
Clinical Data Manager Worldwide Clinical Trials Holdings IncClinical Data ManagerNCProvide fully independent and autonomous leadership of data management services (start up, conduct, and close out) across multiple complex global projects/programs, including: Ensure appropriate resources are allocated to complete all DM activities on time and within budget. We 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.
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 Pharmacist North Carolina license required Shields Health Solutions Holdings LLCClinical Pharmacist North Carolina license requiredNCIdentify trends, resolves problems; recommend improvements; implements change; Actively participates in process improvement initiatives; Protects organization''s value by keeping information confidential; Updates job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations; Willing to do whatever is necessary for the betterment of the Company; Other duties as assigned; Skills: Analyze information, exercise good judgment, possess strong verbal and written communication skills, have deep knowledge of specialty medication pharmacology, local/state/federal pharmacy regulations, able to manage processes, exhibit strong technical and clinical skills, excellent leader and manager of people, constant focus on legal compliance, highly productive, quality focused and attention to detail. Specialties: Knowledge of complex/chronic diseases states and therapies used within specialty pharmacy: Oncology, Transplant, Hepatitis C, Infectious Disease (including HIV), Multiple Sclerosis, Rheumatoid Arthritis, GI disorders (including IBD), Cystic Fibrosis, Psoriasis, Hyperlipidemia and many various inflammatory conditions (including Lupus) preferred.
Mgr Clinical Appeals and Grievances HealthfirstMgr Clinical Appeals and GrievancesNC$103,400–$149,430 / yearPreferred Qualifications: • Experience in clinical practice with a focus in appeals & grievances, claims processing, utilization review or utilization management/case management • Demonstrated understanding of Utilization Review Guidelines (NYS ART 44 and 49 PHL), InterQual, Milliman or Medicare local coverage guidelines • Extensive experience in healthcare appeals • MBA or master's degree from an accredited institution with focus in training & development, education, business, or healthcare administration • Management experience in an operational department within the healthcare industry focused on clinical leadership • Leadership experience in a focus area of operational excellence or audit • Experience developing strategy and processes for a department or function • Experience managing vendors as an extension of a core team • Familiar with creating accountable ownership of a vendor team. Minimum Qualifications: • Bachelor's degree from an accredited institution or equivalent work experience • RN • Experience with utilization management or appeals and grievance processing and compliance • Working experience in a fast-paced environment overseeing multiple priorities, tasks and/or teams • Proven track record of exercising independent thinking, ability to problem solve, understand process flows and correlating platforms to recommend and implement solutions • Experience preparing and delivering written and verbal information to multiple types of audiences • Demonstrated ability to build and foster effective relationships.
Project Leadership - Mid/Large- (clinical trials) - Homebased - (future needs) ParexelProject Leadership - Mid/Large- (clinical trials) - Homebased - (future needs)North CarolinaThe Global Project Leadership department has dedicated members at all levels who are aligned to work with specific types of clients and deliver solutions customized to fit those client’s needs, working on projects spanning across all phases of global clinical trials, in a wide array of therapeutic areas. Parexel has upcoming opportunities in a variety of therapeutics at the Project Leader (PM) and Senior Project Leader (SPM) level for candidates with experience leading global studies in a variety of therapeutics supporting mid to large size biotech/ pharma clients.
Project Leadership – Biotech (Clinical Trials) - Metabolic / GLP-1 / Obesity - Home-Based - (Future Needs) ParexelProject Leadership – Biotech (Clinical Trials) - Metabolic / GLP-1 / Obesity - 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. Individuals selected for these roles will provide leadership to project teams and manage the day-to-day operations while striving to achieve operational excellence through on time delivery within budget and to the highest quality with the goal to exceed client expectations.
Project Leadership – Biotech (clinical trials) –Dermatology - Home Based - (Future Needs) ParexelProject Leadership – Biotech (clinical trials) –Dermatology - 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. Individuals selected for these roles will provide leadership to project teams and manage the day-to-day operations while striving to achieve operational excellence through on time delivery within budget and to the highest quality with the goal to exceed client expectations.
Biotech Project Leadership - Clinical Trials - Home- Based - (Future Needs) ParexelBiotech Project Leadership - Clinical Trials - Home- Based - (Future Needs)North CarolinaParexel has upcoming future 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. Successful 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.
Project Leadership – Biotech (clinical trials) –Respiratory - Home Based - (Future Needs) ParexelProject Leadership – Biotech (clinical trials) –Respiratory - 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. Individuals selected for these roles will provide leadership to project teams and manage the day-to-day operations while striving to achieve operational excellence through on time delivery within budget and to the highest quality with the goal to exceed client expectations.
Project Leadership – Biotech (clinical trials) –Neurology/Psych/Rare Disease - Home Based - (Future Needs) ParexelProject Leadership – Biotech (clinical trials) –Neurology/Psych/Rare Disease - 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. Individuals selected for these roles will provide leadership to project teams and manage the day-to-day operations while striving to achieve operational excellence through on time delivery within budget and to the highest quality with the goal to exceed client expectations.
Project Leadership – Biotech (clinical trials) – Oncology - Home Based - (Future Needs) ParexelProject Leadership – Biotech (clinical trials) – Oncology - 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. Individuals selected for these roles will provide leadership to project teams and manage the day-to-day operations while striving to achieve operational excellence through on time delivery within budget and to the highest quality with the goal to exceed client expectations.
Speech-Language Pathologist Clinical Manager - SLP PediaStaffSpeech-Language Pathologist Clinical Manager - SLPLumberton, NC$72,000–$85,000 / yearMust have completed your CFY plus at least one additional year as a CCC-SLP, Active NC SLP License, Minimum of 2 years of pediatric experience, Strong communication and interpersonal skills, experience treating pediatric and adolescent populations, CPR for all ages, Basic computer proficiency (MS Word preferred), and a passion for mentoring, leadership and clinical excellence. This multi-clinic practice is seeking a Speech-Language Pathologist Clinical Manager who takes a collaborative and multi-disciplinary approach to therapy.
NewRegulatory Affairs Consultant / Senior Consultant - Clinical Regulatory Affairs ParexelRegulatory Affairs Consultant / Senior Consultant - Clinical Regulatory AffairsNorth CarolinaThis highly visible role combines regulatory strategy, global project leadership, health authority engagement, and cross-functional collaboration across programs ranging from early clinical development through registration planning and lifecycle management. Manage and support regulatory submissions and maintenance activities, including IND applications, annual reports, safety submissions, CTA-related activities, protocol amendments, informed consent updates, and end-of-trial deliverables.
Clinical Trial Navigator II JavaraClinical Trial Navigator IIFayetteville, North CarolinaOperate as the lead Clinical Trial Navigator for multiple clinical studies, dependent upon site-specific study needs such as study complexity and enrollment goal volume, by owning the enrollment plan and strategies to achieve and exceed expectations. Ensure scientific integrity of data and record source data appropriately and accurately inclusive of patient visit data within source, CTMS, electronic reporting systems, completing the sponsor’s case report form, and timely query resolution.
Dialysis Clinical Manager Registered Nurse - RN Fresenius Medical Care AG & Co KGaADialysis Clinical Manager Registered Nurse - RNFayetteville, NCOther: Collaborates closely with, providing oversight as needed to, the Clinical Manager/Charge RN acting as nurse manager, the Medical Director, and the physicians regarding the direct patient care responsibilities within the facility to ensure the provision of outstanding quality of patient care, as defined by the FMS quality goals, and compliance with the pertinent company policies and procedures. Demonstrated leadership competencies and management skills for the position, including excellent communication, customer service, continuous quality improvement, relationship development, results orientation, team building, motivating employees, performance management and decision making.
Associate Director, Operations - Clinical Assessment Technologies (CAT) - US/Canada - Remote Worldwide Clinical Trials Holdings IncAssociate Director, Operations - Clinical Assessment Technologies (CAT) - US/Canada - RemoteNCRemote$112,000–$223,000 / 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. Development Operations is a team of highly experienced Business Development professionals who drive significant bookings targets and support Worldwide's strategic position in a competitive market through a culture of collaboration and innovation.
Clinical Specialist, Vessel Closure - Fayetteville/Raleigh, NC Abbott LaboratoriesClinical Specialist, Vessel Closure - Fayetteville/Raleigh, NCFayetteville, NC$61,300–$122,700 / yearEducate customers on the merits and proper clinical usage of company products by giving presentations and demonstrations using a wide variety of formats and platforms (e.g., slides, transparencies, manuals) to keep all customers abreast of the latest product, therapy, and technology developments and current items of interest in the industry. Respond to customer needs and complaints regarding products and service by developing creative and feasible solutions or working with other related personnel (e.g., sales, clinical research, marketing, product development) to develop optimal solutions.
Clinical Specialist, Vessel Closure - Fayetteville/Raleigh, NC AbbottClinical Specialist, Vessel Closure - Fayetteville/Raleigh, NCFayetteville, North CarolinaContinuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Driving a personal auto or company car or truck, or a powered piece of material handling equipment, Keyboard use (greater or equal to 50% of the workday) . Educate customers on the merits and proper clinical usage of company products by giving presentations and demonstrations using a wide variety of formats and platforms (e.g., slides, transparencies, manuals) to keep all customers abreast of the latest product, therapy, and technology developments and current items of interest in the industry.
Clinical Scientist - Vaccine Syneos HealthClinical Scientist - VaccineNorth CarolinaCollaborates with study team members including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management (set-up and/or lead meetings as appropriate) to identify risks related to data integrity and subject safety. Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
Clinical Scientist - Respiratory Syneos HealthClinical Scientist - RespiratoryNorth CarolinaCollaborates with study team members including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management (set-up and/or lead meetings as appropriate) to identify risks related to data integrity and subject safety. Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
Clinical Scientist - Oncology Syneos HealthClinical Scientist - OncologyNorth CarolinaCollaborates with study team members including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management (set-up and/or lead meetings as appropriate) to identify risks related to data integrity and subject safety. Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.