Sr. Clinical Trials Manager Agilent Technologies IncSr. Clinical Trials ManagerVAMonitor and review study budget and data management activities, such as PRF development, training, and facilitating query resolution with proper documentation • Support monitoring efforts by setting quality and compliance goals by overseeing and approving study monitoring plans, may review, suggest edits and approve monitoring trip reports • Contribute to contract review and negotiations with outside vendors and study sites or laboratories • Mentor CTMs and CRAs • Demonstrate an ability to influence others to achieve positive results and collaboration through diplomacy and respect for others, appropriate prioritization and facilitation of the decision-making process Qualifications Qualifications: • Bachelors degree or higher, or equivalent credentials • Knowledge of GCP, ICH guidelines, and other clinical regulatory requirements • Strong interpersonal skills (verbal and written), organizational, and prioritization skills, able to communicate at multiple levels of an organization and with sponsors/clients. Primary Responsibilities (all levels): • Manage, design and implement all clinical operational aspects of IVD clinical trials from inception through close-out • Serve as main point of contact for internal and external study stakeholders; effectively communicating, collaborating, managing escalation of issues, where necessary, as well as participating and leading internal and external study meetings • Identify, evaluate, and oversee qualification and contracting for study investigators, study sites, CRO and/or vendor management for the study, where applicable • Develop or assist in the development of study-related plans and documents including protocols, informed consent forms, monitoring plans, case report forms, training plans and engagement materials • Ensure trial master file (TMF/eTMF) is established, current, and maintained per ICH E6.
Per Diem Clinical Research Nurse - Home Visits Science 37 IncPer Diem Clinical Research Nurse - Home VisitsRichmond, VA$50–$55 / hourWith interest/expertise in Science 37's decentralized model of care delivery, the Mobile Research Nurse will perform delivery of care to participants as well as collaborate with brick and mortar sites, if indicated, for shared clinical trial implementation. Science 37's Nursing Solutions Group brings together expert nurses who share a passion for organizing, planning and implementing mobile clinical nurse services to participants in clinical trials.
Per Diem Clinical Research Nurse - Home Visits Science 37Per Diem Clinical Research Nurse - Home VisitsRichmond, VA$50–$55 / hourWith interest/expertise in Science 37's decentralized model of care delivery, the Mobile Research Nurse will perform delivery of care to participants as well as collaborate with brick and mortar sites, if indicated, for shared clinical trial implementation. Science 37's Nursing Solutions Group brings together expert nurses who share a passion for organizing, planning and implementing mobile clinical nurse services to participants in clinical trials.
Clinical Research Coordinator 2, Joint Emerging Diseases Initiative (JEDI) Commonwealth of VirginiaClinical Research Coordinator 2, Joint Emerging Diseases Initiative (JEDI)Charlottesville, VAProcess, prepare and ship study research samples Ability to work a flexible schedule, when needed, given the nature of the studies open to enrollment Ability to work on weekends, when needed, given the nature of the studies open to enrollment Ability to enroll COVID positive patients in the inpatient or outpatient settings Ability to draw blood when necessary, or become phlebotomy trained Support and providing guidance to faculty and trainees with clinical research projects in the department. The Division of Infectious Diseases & International Health at the University of Virginia (UVA) School of Medicine is currently seeking applicants for a Clinical Research Coordinators (CRC), non-licensed or licensed, that has the skill and experience of a CRC 2 to join the JEDI clinical trials team to assist with oversight of multiple clinical research projects.
Clinical Research Coordinator 2-3, Joint Emerging Diseases Initiative (JEDI) Commonwealth of VirginiaClinical Research Coordinator 2-3, Joint Emerging Diseases Initiative (JEDI)Charlottesville, VA$62,000–$70,000 / yearp>blocks--linked-image#click keydown.enter->blocks--linked-image#click" data-controller="" data-open-newtab="false" id="page_block_1abc4ef3edc569846f0d83e2f82d8d57" style="background-image: linear-gradient(rgba(0, 0, 0, 0.5),rgba(0, 0, 0, 0.5)), url("https://d25wby5c7p9100.cloudfront.net/public/uploads/599e9569ce634cc6f690338b21af637e/images/files/b11c644db1e4b7c02146bb405507b1a2/large/mountainview.jpg?1674243607");background-position: 50% 50%" title="Virginia Mountain View">. The Division of Infectious Diseases & International Health at the University of Virginia (UVA) School of Medicine is currently seeking applicants for a Clinical Research Coordinators (CRC), non-licensed or licensed, that has the skill and experience of a CRC2 or CRC3 to join the JEDI clinical trials team to assist with oversight of multiple clinical research projects.
Investigator Initiated Trial Research Operations Project Manager Commonwealth of VirginiaInvestigator Initiated Trial Research Operations Project ManagerRichmond, VAResearch Administrators often serve as a key point of contact between the university and the research sponsor, research project staff, and participants, ensuring effective coordination and communication across all stakeholders involved in study development and conduct; Maintain systems and processes for managing at both a project and a program level, including development and tracking of project timelines, study start-up activities, and key study milestones; Work closely with Principal Investigators (PI), study staff, unit administrators, and coordinate with central offices in pre and/or post award stages of project management; as well as providing research program level reporting and analytics to leadership, while facilitating cross-functional coordination (e.g., regulatory, data management, and clinical operations) to support study activation and ongoing execution; Support and coordinate study start-up activities, including feasibility assessment, site readiness, and activation planning, ensuring studies are prepared for timely execution; Oversee and coordinate activities across participating sites or teams, ensuring consistency in study conduct and timely resolution of issues; Identify potential risks, delays, or gaps in project execution and proactively implement mitigation strategies; Track and report study progress, including key milestones such as activation, enrollment, and study completion, to support leadership oversight and decision-making; Other duties as assigned. Bachelor"s degree or equivalent applicable combination of training, education and experience required; Candidates whose resumes highlight the following previous experience will be prioritized: Demonstrated experience working in and fostering an environment of respect, professionalism and civility with a population of faculty, staff, and students from various backgrounds and experiences, or a commitment to do so as a staff member at VCU; Advanced proficiency with data entry and word processing skills, with the ability to analyze and interpret information effectively; Advanced organizational abilities and a keen eye for detail to ensure accuracy and efficiency in all tasks with the ability to multitask and prioritize autonomously; Clear and professional written and verbal communication skills, with the ability to interact effectively with colleagues and stakeholders; Interpersonal skills, capable of building relationships and collaborating with team members at all levels to gather information and support compliance efforts; Problem-solving and organizational aptitude, with the ability to manage multiple tasks, meet deadlines in a dynamic environment and independently make critical decisions.
Clinical Research Coordinator I - Nurse- Richmond, VA Iterative Scopes IncClinical Research Coordinator I - Nurse- Richmond, VARichmond, VABy combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies.
Clinical Research Coordinator 2; Plastic Surgery Commonwealth of VirginiaClinical Research Coordinator 2; Plastic SurgeryCharlottesville, VAWith excellence in physician leadership, research, education, and innovations, we strive to improve perioperative outcomes, establish unparalleled practices in patient care, and advance the field of plastic surgery globally. This position coordinates and implements clinical trial research studies, works closely with the Principal Investigators, Operational Managers, and other research team members during the performance of the trials.
Clinical Research Coordinator II - Richmond, VA Iterative Scopes IncClinical Research Coordinator II - Richmond, VARichmond, VALead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies, with accountability for achieving enrollment goals. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.
Oncology Research Manager Riverside HospitalOncology Research ManagerNewport News, VirginiaSupervises research work to include the following but not limited to listed duties - resource to research coordinators, train as needed, work as a coordinator, manage productivity/workload, compliance for studies and regulatory and work closely with physicians for study selection. Maintain a professional courteous and considerate demeanor in all interactions with RMG practices, facility and support service team members, research team members, caregivers, patients and visitors.
Registered Nurse (RN), Clinical Research — Physician Office — Cancer Institute Medical Oncology Bon Secours Mercy HealthRegistered Nurse (RN), Clinical Research — Physician Office — Cancer Institute Medical OncologyMidlothian, VirginiaEssential Job Functions : Enroll patients in research studies, associating visits / appointments / admissions with research studies and reviewing charges via the Research Billing Report to determine which are billed to Insurance and which are billed to the research study. Obtain required medical information from patients, advise patients of visits, assign numbers to the patients as required by protocol, and ensure that all study-related documentation, forms, CRF’s, are complete.
Clinical Research Nurse, Clinical Operations Commonwealth of VirginiaClinical Research Nurse, Clinical OperationsRichmond, VARecruitment, Enrollment, Retention, and Data Collection A CRN drives study coordination and regulatory management with participant recruitment, enrollment, tracking, data collection, data processing, resolution of discrepancies, queries, etc., verification, case-finding, evaluation, abstraction of source documentation, case report form completion, database use, management, data abstraction, organization, and archiving of data in the study database for research studies. Mission To reduce the state cancer burden for all Virginians by addressing the confluence between biological, social, and policy drivers through high-impact, cutting-edge research, person-centered care across the continuum from prevention through survivorship, community integration, and training the next generation of community-centric researchers and healthcare professionals.
Investigator Initiated Trial Research Operations Project Manager Virginia Commonwealth UniversityInvestigator Initiated Trial Research Operations Project ManagerRichmond, VAResearch Administrators often serve as a key point of contact between the university and the research sponsor, research project staff, and participants, ensuring effective coordination and communication across all stakeholders involved in study development and conduct; Maintain systems and processes for managing at both a project and a program level, including development and tracking of project timelines, study start-up activities, and key study milestones; Work closely with Principal Investigators (PI), study staff, unit administrators, and coordinate with central offices in pre and/or post award stages of project management; as well as providing research program level reporting and analytics to leadership, while facilitating cross-functional coordination (e.g., regulatory, data management, and clinical operations) to support study activation and ongoing execution; Support and coordinate study start-up activities, including feasibility assessment, site readiness, and activation planning, ensuring studies are prepared for timely execution; Oversee and coordinate activities across participating sites or teams, ensuring consistency in study conduct and timely resolution of issues; Identify potential risks, delays, or gaps in project execution and proactively implement mitigation strategies; Track and report study progress, including key milestones such as activation, enrollment, and study completion, to support leadership oversight and decision-making; Other duties as assigned. Bachelor''s degree or equivalent applicable combination of training, education and experience required; Candidates whose resumes highlight the following previous experience will be prioritized: Demonstrated experience working in and fostering an environment of respect, professionalism and civility with a population of faculty, staff, and students from various backgrounds and experiences, or a commitment to do so as a staff member at VCU; Advanced proficiency with data entry and word processing skills, with the ability to analyze and interpret information effectively; Advanced organizational abilities and a keen eye for detail to ensure accuracy and efficiency in all tasks with the ability to multitask and prioritize autonomously; Clear and professional written and verbal communication skills, with the ability to interact effectively with colleagues and stakeholders; Interpersonal skills, capable of building relationships and collaborating with team members at all levels to gather information and support compliance efforts; Problem-solving and organizational aptitude, with the ability to manage multiple tasks, meet deadlines in a dynamic environment and independently make critical decisions.
Registered Nurse (RN), Clinical Research - Physician Office - Cancer Institute Medical Oncology Bon Secours Mercy Health IncRegistered Nurse (RN), Clinical Research - Physician Office - Cancer Institute Medical OncologyVAEssential Job Functions : Enroll patients in research studies, associating visits / appointments / admissions with research studies and reviewing charges via the Research Billing Report to determine which are billed to Insurance and which are billed to the research study. Obtain required medical information from patients, advise patients of visits, assign numbers to the patients as required by protocol, and ensure that all study-related documentation, forms, CRF's, are complete.
Clinical Research Coordinator 2, Joint Emerging Diseases Initiative (JEDI) University of VirginiaClinical Research Coordinator 2, Joint Emerging Diseases Initiative (JEDI)Charlottesville, VAProcess, prepare and ship study research samples Ability to work a flexible schedule, when needed, given the nature of the studies open to enrollment Ability to work on weekends, when needed, given the nature of the studies open to enrollment Ability to enroll COVID positive patients in the inpatient or outpatient settings Ability to draw blood when necessary, or become phlebotomy trained Support and providing guidance to faculty and trainees with clinical research projects in the department. The Division of Infectious Diseases & International Health at the University of Virginia (UVA) School of Medicine is currently seeking applicants for a Clinical Research Coordinators (CRC), non-licensed or licensed, that has the skill and experience of a CRC 2 to join the JEDI clinical trials team to assist with oversight of multiple clinical research projects.
Clinical Research Coordinator 2-3, Joint Emerging Diseases Initiative (JEDI) University of VirginiaClinical Research Coordinator 2-3, Joint Emerging Diseases Initiative (JEDI)Charlottesville, VA$62,000–$70,000 / yearp>The Division of Infectious Diseases & International Health at the University of Virginia (UVA) School of Medicine is currently seeking applicants for a Clinical Research Coordinators (CRC), non-licensed or licensed, that has the skill and experience of a CRC2 or CRC3 to join the JEDI clinical trials team to assist with oversight of multiple clinical research projects. Currently we have 2 inpatient trials (ARDS & Viral PNA), 1 acute COVID outpatient trial, 2 Long COVID outpatient trials in close-out and soon we will have 3 new Long COVID trials in startup.
Clinical Site Manager CRA - Richmond Charlottesville Northern VA Astellas Pharma IncClinical Site Manager CRA - Richmond Charlottesville Northern VACharlottesville, VAThe Site Manager will partner with Clinical Trial Lead (CTL,) Clinical Trial Manager (CTM,) Clinical Trial Specialist (CTS,) and Study Start-Up Specialist (SSS) to ensure overall site management while performing trial related activities for assigned protocols. Responsible for driving activities within site initiation and start-up, preparation and conduct of site monitoring (including remote monitoring), site management (by study specific systems and other reports/dashboards) and site/study close-out according to SOPs, Work Instructions (WIs) and policies.
Clinical Research Site Director Alcanza Clinical Research LLCClinical Research Site DirectorCharlottesville, VAOverseeing resourcing allocations, site assignments, and study team members output and performance to ensure study deliverables are on track, identifying risks to delivery or quality and escalating any risks to clinical trial management deliverables timeline, quality, and budget. Collaborating with department leaders in Business Development, Patient Recruitment, Finance and Budgets, Contracts and Quality to coordinate delivery expectations, meet expected study milestones such as site activation targets, enrollment targets, etc., meet budgets and delivery quality data to sponsors.
Clinical Research Associate, Sponsor Dedicated IQVIA Holdings IncClinical Research Associate, Sponsor DedicatedVAEnsure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Clinical Research Physician - part time - Open to either Psychiatrist, Obesity medicine Alcanza Clinical ResearchClinical Research Physician - part time - Open to either Psychiatrist, Obesity medicineCharlottesville, VirginiaEssential Job Duties:Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes . The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes.
Clinical Research Physician - part time - Open to either Neurologist, Psychiatrist, Obesity, Dermatologist Alcanza Clinical Research LLCClinical Research Physician - part time - Open to either Neurologist, Psychiatrist, Obesity, DermatologistCharlottesville, VAp>• Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials in adherence with FDA, ICH, NIH, GCPs, & HIPAA guidelines, study protocols, as well as company policies and processes. The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH, FDA, DAGCP, guidelines, local regulations, study protocol, and company policies and processes.
Clinical Research Coordinator II - Richmond, VA Iterative HealthClinical Research Coordinator II - Richmond, VARichmond, VABy combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies, with accountability for achieving enrollment goals.
Clinical Research Coordinator (varying levels), Pulmonary and Critical Care Commonwealth of VirginiaClinical Research Coordinator (varying levels), Pulmonary and Critical CareCharlottesville, VAThe Division of Pulmonary and Critical Care Medicine at the University of Virginia's (UVA) School of Medicine is seeking applicants for a Clinical Research Coordinator 2 Licensed or Non-licensed or Clinical Research 3 Licensed or Non-licensed, to participate in clinical trials and registries. This position works closely with world-renowned Principal Investigators and other research team members who specialize in pulmonary fibrosis and sarcoidosis, diseases that cause progressive scarring of the lungs and shortness of breath.
Clinical Research Nurse, SOM, Stravitz-Sanyal Institute for Liver Disease Commonwealth of VirginiaClinical Research Nurse, SOM, Stravitz-Sanyal Institute for Liver DiseaseRichmond, VA$57,900–$95,900 / yearThe Stravitz-Sanyal Liver Institute of Virginia Commonwealth University is seeking a Clinical Research Nurse to join its world-renowned team of Hepatologists, researchers, and imaging experts in changing the landscape of liver and metabolic diseases through research. Maintain current CITI credentials for Human Subjects Protections, Good Clinical Practice (GCP), Clinical Research Coordinator, plus additional sponsor GCP certifications as required.
Clinical Research Coordinator - School of Medicine, Neurology Commonwealth of VirginiaClinical Research Coordinator - School of Medicine, NeurologyRichmond, VA$55,000–$57,300 / yearTypical duties of a Clinical Research Coordinators include but are not limited to: assist the PI in assessing study feasibility, determining participation eligibility, and establishing guidelines for clinical data collection; serve as patient/participant recruiters; and perform a variety of complex activities involved in the collection, compilation, documentation, and analysis of clinical research data. The Department of Neurology has a talented, robust team of faculty members and staff spanning nine divisions which includes representatives from every neurology subspecialty in adult and child neurology, plus award-winning educators, clinical and translational neuroscientists and master clinicians.
Clinical Research Coordinator - SOM/Pediatrics Commonwealth of VirginiaClinical Research Coordinator - SOM/PediatricsRichmond, VAJob duties may include entering information into the medical record; provide documentation assistance with transcribing provider orders; performing study assessments, including point of care testing; providing documentation assistance with transcribing provider orders in EPIC; the handling, transportation, access to and/or contact with medications and related supplies; minimum qualifications include HIPAA training, EMR navigation/computerized order entry. Tasks may include attend clinics/rounds to discuss studies with patients and care team members, screen patient charts, determine eligibility for multiple studies, develop recruitment plans and reports of expected vs observed enrollment rate, etc.
Manager, Inova Schar Heart & Vascular Research Program Inova Health SystemManager, Inova Schar Heart & Vascular Research ProgramFalls Church, VAManager, ISHV Research Program Responsibilities: Oversees assigned department or functional area to ensure it is performing effectively, which may include but not limited to, hiring and training team members, creating and implementing business strategies, managing performance of team members, and delegating tasks. Develops and oversees research study budget, negotiation and implementation to ensure selected research studies have an adequate subject population and will result in financially and academically productive research.
Lead Clinical Data Manager (Remote) IQVIA Holdings IncLead Clinical Data Manager (Remote)Virginia Beach, VARemoteYour previous roles/job titles may include Clinical Data Manager, Senior Clinical Data Manager, Lead Data Manager, Principal Data Manager, and/or Data Management Project Manager. IQVIA is seeking experienced Clinical Data Management Leads to oversee end-to-end data management delivery for global clinical trials.
Clinical Research Coordinator 621500 Commonwealth of VirginiaClinical Research Coordinator 621500Richmond, VA$52,500–$55,000 / yearli>Strong communication skills, both written and verbal, excellent interpersonal/organizational skills; Strong interpersonal skills such as establishing rapport, maintaining participant motivation, empathic responding, ability to work effectively as part of a multidisciplinary team, and ability to use clinical judgment in (rare) emergency situations. Under the supervision of the Principal Investigator and project manager, the incumbent will collaborate with all members of the research teams, to ensure all federal, state, university, and protocol requirements are followed, institutional research objectives are met, and ethical obligations are kept.
Sr. Clinical Data Manager Karwell TechnologiesSr. Clinical Data ManagerRichmond, VAFacilitate cross-functional Data Management meetings with Study Managers, Project Managers, Programming, and Regulatory teams. Develop and manage study timelines and ensure the quality and timeliness of data from service providers (e.g., Central Reading Centers, Labs, Medical Coders).
Clinical Analyst- Research Registered Nurse U.S. Department of Veterans AffairsClinical Analyst- Research Registered NurseRichmond, VA$82,228–$163,760 / yearMSN and 2 years of specialized nursing experience, one of which is equivalent to Nurse II and meets all dimension requirements for Nurse III; OR a Masters degree in related field with BSN and two years of specialized nursing experience, one of which is equivalent to Nurse II and meets all dimension requirements for Nurse III; OR a Doctoral degree in Nursing with and one year of specialized nursing experience equivalent to Nurse II and meets all dimension requirements for Nurse III; OR a Doctoral degree in a related field with a BSN and one year of specialized nursing experience equivalent to Nurse II and meets all dimension requirements for Nurse III. Graduate of a school of professional nursing approved by the appropriate accrediting agency and accredited by one of the following accrediting bodies at the time the program was completed by the applicant: The Accreditation Commission for Education in Nursing (ACEN) or The Commission on Collegiate Nursing Education (CCNE); OR Individuals attending a masters level bridge program in nursing who have completed coursework equivalent to a bachelors level degree in Nursing may have opportunity to become registered as a nurse with a state licensing board prior to completion of the bridge program.
Clinical Research Coordinator 4, Post-Award Supervisor Commonwealth of VirginiaClinical Research Coordinator 4, Post-Award SupervisorCharlottesville, VAli>Work with the Clinical Trials leadership to manage a team of Clinical Research Coordinators and/or laboratory or research support staff, with responsibilities that include hiring, scheduling, workload management, compensation, rewards, professional development, and performance management. The CRC in this role is able to work independently and has the authority to interact with internal or external stakeholders involved in a clinical trial or modify clinical trial workflow or processes within their respective Department or Division to meet the needs of a given study.
Clinical Research Coordinator 3, Non-licensed; Asthma, Allergy and Immunology Commonwealth of VirginiaClinical Research Coordinator 3, Non-licensed; Asthma, Allergy and ImmunologyCharlottesville, VAli>May manage or lead a team of Clinical Research Coordinators and/or laboratory or research support staff, with responsibilities that include hiring, scheduling, workload, compensation, rewards, professional development, and performance management. Demonstrate a high level of proficiency with the various electronic platforms utilized in clinical research such as: IRB Pro, Protocol Builder, CRConnect, OnCore, e-regulatory platforms and Epic.
Senior Research Operations Manager IVPRL, Department of Surgery Commonwealth of VirginiaSenior Research Operations Manager IVPRL, Department of SurgeryRichmond, VA$80,000–$90,000 / yearp>Manage all IRB submissions, amendments, continuing reviews, and protocol adherence Prepare and submit annual reports, RPPR closeout reports, and milestone updates for NIH and CDC grants Ensure compliance with federal regulations and internal policies related to research conduct, ethics, and data protection Work with industry on industry-sponsored research. Coordinate administrative tasks and timelines for new grant submissions Manage budgets, personnel allocations, and procurement for active projects Oversee and be responsible for data sharing plans and reporting to NIH, including NIMH Data Archive uploads and tracking project milestones.
Clinical Research Coordinator (varying levels), Pulmonary and Critical Care University of VirginiaClinical Research Coordinator (varying levels), Pulmonary and Critical CareCharlottesville, VAThe Division of Pulmonary and Critical Care Medicine at the University of Virginia's (UVA) School of Medicine is seeking applicants for a Clinical Research Coordinator 2 Licensed or Non-licensed or Clinical Research 3 Licensed or Non-licensed, to participate in clinical trials and registries. This position works closely with world-renowned Principal Investigators and other research team members who specialize in pulmonary fibrosis and sarcoidosis, diseases that cause progressive scarring of the lungs and shortness of breath.
Clinical Informatics Program Manager LifeNet Health IncClinical Informatics Program ManagerRichmond, VA$87,226–$116,301 / yearWHAT YOU'LL BRING Minimum Requirements: Bachelor's Degree - Healthcare related field (nursing, allied health, or health informatics) FIVE (5) Years - Experience supporting healthcare technology or working extensively with Electronic Medical Records or Electronic Health Record systems SEVEN (7) Years - Clinical experience within the hospital setting to include critical care, medical/surgical, trauma, ER, pediatrics, cardiovascular, surgical, or transplant center Preferred Experience/Skills/Certifications: Master's Degree - Healthcare related field (nursing, allied health, or health informatics) SEVEN (7) Years - Experience supporting healthcare technology or working extensively with Electronic Medical Records or Electronic Health Record systems TEN (10) Years - Clinical experience within the hospital setting to include critical care, medical/surgical, trauma, ER, pediatrics, cardiovascular, surgical, or transplant center THREE (3) Years - Clinical consulting experience in clinical workflow analysis or process design NI-BC - Nursing Informatics Board Certification PMP - Project Management Certification Key Knowledge, Skills, & Abilities: Organ Donation and Healthcare Operations Process Knowledge: Strong understanding of the organ donation and healthcare operations processes. In this position, you'll be responsible for designing, implementing, and maintaining clinical information systems, including but not limited to Electronic Medical Records (EMRs) - both OPO and donor hospitals, integrated OPO systems, and reporting output, to improve operational workflows to maximize donation opportunities.
Clinical Research Coordinator - School of Medicine, Neurology Virginia Commonwealth UniversityClinical Research Coordinator - School of Medicine, NeurologyRichmond, VA$55,000–$57,300 / yearTypical duties of a Clinical Research Coordinators include but are not limited to: assist the PI in assessing study feasibility, determining participation eligibility, and establishing guidelines for clinical data collection; serve as patient/participant recruiters; and perform a variety of complex activities involved in the collection, compilation, documentation, and analysis of clinical research data. The Department of Neurology has a talented, robust team of faculty members and staff spanning nine divisions which includes representatives from every neurology subspecialty in adult and child neurology, plus award-winning educators, clinical and translational neuroscientists and master clinicians.
Clinical Research Coordinator - SOM/Pediatrics Virginia Commonwealth UniversityClinical Research Coordinator - SOM/PediatricsRichmond, VAJob duties may include entering information into the medical record; provide documentation assistance with transcribing provider orders; performing study assessments, including point of care testing; providing documentation assistance with transcribing provider orders in EPIC; the handling, transportation, access to and/or contact with medications and related supplies; minimum qualifications include HIPAA training, EMR navigation/computerized order entry. Tasks may include attend clinics/rounds to discuss studies with patients and care team members, screen patient charts, determine eligibility for multiple studies, develop recruitment plans and reports of expected vs observed enrollment rate, etc.
Clinical Research Nurse, SOM, Stravitz-Sanyal Institute for Liver Disease Virginia Commonwealth UniversityClinical Research Nurse, SOM, Stravitz-Sanyal Institute for Liver DiseaseRichmond, VA$57,900–$95,900 / yearConsults with appropriate research staff on participant devices and contraindications as needed • Obtain participant vascular access, vital signs as needed and other clinical duties in caring for research imaging participants during visit • Administers investigational medications and performs patient assessments during clinic visits to determine presence of side effects • Work with research staff to monitor participants post-injection while following all reaction protocols per ACR guidelines • Provides accurate and timely data collection, documentation, entry, and reporting in either internal and sponsor databases • Works with technologists on protocol questions, and participates in other operational tasks within the Imaging Center as needed including administrative duties such as maintaining inventory, staffing operations, and participant scheduling • Work with Associate Director of Clinical Trials to ensure best practice guidelines are followed for the research participant in areas such as study activation, study coordination, data management, and records management • Maintain current CITI credentials for Human Subjects Protections, Good Clinical Practice (GCP), Clinical Research Coordinator, plus additional sponsor GCP certifications as required. • Understand and adhere to all IRB requirements, Human Subjects protection regulations, and all aspects of IRB approved protocols • Ensures site compliance with research protocols by reviewing all regulatory requirements to confirm implementation of appropriate methods, practices, and procedures for all research activities • Ensures compliance with research protocols, by providing ongoing quality control audits, including maintaining ongoing investigational drug accountability • Maintain appropriate training, licensure and certifications per job requirements • Engage with staff and departmental leadership to streamline research workflow and operational efficiencies, while ensuring compliance to MRI and PET/CT policy and procedures • Perform quality assurance procedures and implement process improvement changes as required • Serve as an ongoing resource for providing information and expert advice on clinical research issues.
Clinical Research Coordinator II (31515) GI AllianceClinical Research Coordinator II (31515)VAli>Acts as an experienced resource for Clinical Research Coordinators I and Research Assistants during new hire training, newly initiated trials, and trial transitions. JOB RELATIONSHIPS: Reports to the Clinical Research Director, Vice President of Research, Market President, and the physicians at the local Market Clinic.
Clinical Research Coordinator 621500 Virginia Commonwealth UniversityClinical Research Coordinator 621500Richmond, VA$52,500–$55,000 / yearStrong communication skills, both written and verbal, excellent interpersonal/organizational skills; Strong interpersonal skills such as establishing rapport, maintaining participant motivation, empathic responding, ability to work effectively as part of a multidisciplinary team, and ability to use clinical judgment in (rare) emergency situations. Under the supervision of the Principal Investigator and project manager, the incumbent will collaborate with all members of the research teams, to ensure all federal, state, university, and protocol requirements are followed, institutional research objectives are met, and ethical obligations are kept.
RN Clinical Research Coordinator III Virginia Commonwealth University HealthRN Clinical Research Coordinator IIIRichmond, VAThis may include, but is not limited to, administrative and clinical processes, project initiation and maintenance, enrollment of patients, designing of case report forms, data collection, managing study patient follow-up, coordination of monitoring visits, collaborative writing of protocols and reports, and other administrative duties as determined for the successful conduct of innovative clinical research projects. Experience Preferred: Over eight (8) years of work experience in clinical research; Eight (8) years of work experience in disease/discipline; Extensive patient records review and abstraction experience; Over eight (8) years of work experience in a team environment; Publication experience; Protocol development experience; and Management of clinical research staff.
Clinical Research Coordinator 3, Non-licensed; Asthma, Allergy and Immunology University of VirginiaClinical Research Coordinator 3, Non-licensed; Asthma, Allergy and ImmunologyCharlottesville, VAMay manage or lead a team of Clinical Research Coordinators and/or laboratory or research support staff, with responsibilities that include hiring, scheduling, workload, compensation, rewards, professional development, and performance management. Demonstrate a high level of proficiency with the various electronic platforms utilized in clinical research such as: IRB Pro, Protocol Builder, CRConnect, OnCore, e-regulatory platforms and Epic.
Clinical Research Coordinator 4, Post-Award Supervisor University of VirginiaClinical Research Coordinator 4, Post-Award SupervisorCharlottesville, VAli>Work with the Clinical Trials leadership to manage a team of Clinical Research Coordinators and/or laboratory or research support staff, with responsibilities that include hiring, scheduling, workload management, compensation, rewards, professional development, and performance management. The CRC in this role is able to work independently and has the authority to interact with internal or external stakeholders involved in a clinical trial or modify clinical trial workflow or processes within their respective Department or Division to meet the needs of a given study.
Clinical Nurse Manager (RN) - IMCU (Intermediate Care Unit) Sentara Healthcare IncClinical Nurse Manager (RN) - IMCU (Intermediate Care Unit)Norfolk, VAJoin a team that has a mission to improve health every day and a vision to be the healthcare choice of the communities that we serve! keywords: #Indeed, Talroo - Nursing, clinical manager, nursing leadership, stepdown, IMCU, intermediate care, medical/surgical, med/surg, supervisor, manager, clinical leader. We are also home to the region's only 24-hour hyperbaric oxygen program that helps speed up the healing of carbon monoxide poisoning, wounds that won't heal, infections in which tissues are starved for oxygen, airborne chemical exposures, and scuba diving accidents.
Clinical Case Manager St Joseph's VillaClinical Case ManagerRichmond, VAProvides intensive case coordination using the High-Fidelity Wraparound model for individuals and families in coordination with Community Service Boards (CSB) and other appropriate organization including but not limited to schools, physicians, private providers, etc. to support stabilization upon discharge. Clinical Case Manager coordinates the overall services provided to individuals with external agencies and provides targeted discharge linkages for individuals to ensure ongoing stabilization for the next appropriate level of care.
Program Manager, Research Compliance Children's Hospital of The King's DaughtersProgram Manager, Research ComplianceNorfolk, VALICENSES AND/OR CERTIFICATIONS Required Licenses and/or Certifications MINIMUM EDUCATION AND EXPERIENCE REQUIREMENTS Required Education and Experience Bachelors degree in relevant fields such as biology, public health, or regulatory affairs. ESSENTIAL DUTIES AND RESPONSIBILITIES Program Administration: Provides research compliance program administration by interpreting and applying research compliance rules and regulations for the university and its community, research sponsors, and regulatory entities.
Category Manager, Clinical Contracts Owens & MinorCategory Manager, Clinical ContractsVirginiaThe Category Manager (Clinical Contract Steward) is an experienced sourcing and contracting professional responsible for owning the post‑award lifecycle of clinical sourcing contracts and ensuring that negotiated value is fully realized, governed, and sustained. Owens & Minor is a global healthcare solutions company providing essential products, services and technology solutions that support care delivery in leading hospitals, health systems and research centers around the world.
Clinical Research Site Director Alcanza Clinical ResearchClinical Research Site DirectorCharlottesville, VirginiaCollaborating with department leaders in Business Development, Patient Recruitment, Finance, and Budgets Contracts and Quality to coordinate delivery expectations, meet expected study milestones (such as site activation targets, enrollment targets, etc.), meet budgets, and delivery quality data to sponsors. Overseeing resourcing allocations, site assignments and study team members' output and performance, to ensure study deliverables are on track, identifying risks to delivery or quality, and escalating any risks to clinical trial management deliverables (timeline, quality and budget).
Mgr Clinical Appeals and Grievances HealthfirstMgr Clinical Appeals and GrievancesVA$103,400–$149,430 / yearp>Preferred 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.