NewAssistant/Associate Professor - Geriatrics EVMSAssistant/Associate Professor - GeriatricsNorfolk, VAThe historic port city of Norfolk, where EVMS is located, is centrally positioned in the bustling 1.8 million-person Hampton Roads area, with easy access to local colleges, universities, and 144 miles of stunning shoreline. As part of the Glennan Center for Geriatrics and Gerontology as well as the Goldrich Institute for Integrated NeuroHealth, we advance Geriatric and Palliative care Medicine practices through interdisciplinary collaboration.
Regional Clinical Research Associate (REMOTE) Teleflex IncRegional Clinical Research Associate (REMOTE)VARemote$105,000–$115,000 / yearo Identification of data discrepancies and compliance concerns, present findings to site research staff, provide retraining if needed, provide problem-solving strategies and communicate findings to the study team and department management via escalation of issues and/or within the monitoring visit report. Our current Interventional products include a broad range of clinically relevant solutions, such as our GuideLiner and Turnpike Catheters, Ringer Perfusion Balloon Catheter, AC3 Optimus and AC3 Range Intra-Aortic Balloon Pumps and the OnControl Powered Bone Access System.
Clinical Research Associate, Sponsor Dedicated IQVIA Holdings IncClinical Research Associate, Sponsor DedicatedVAp>• Ensure 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.
Grant Funded Department of Medicine Clinical Research Unit - Clinical Research Coordinator I Carilion Medical CenterGrant Funded Department of Medicine Clinical Research Unit - Clinical Research Coordinator IRoanoke, VirginiaDevelops and maintains patient databases and study maintenance logs including but not limited to training logs, delegation of responsibility logs, screening logs, enrollment logs, and investigational product log. Under general supervision of the Principal Investigator, the Clinical Research Coordinator I assists with administrative activities associated with the conduct of research studies including industry sponsored, grant funded or internally funded studies while maintaining compliance with guidelines set by governing agencies and institutional policy.
Sr. Clinical Research Associate, IQVIA IQVIA Holdings IncSr. Clinical Research Associate, IQVIAFairfax, VADeprecated: preg_replace(): Passing null to parameter #3 ($subject) of type array|string is deprecated in C:\api\public\classes\StringCleaner.class.php on line 85.
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.
Part-time Clinical Research Coordinator 3; Center for Psychiatric Clinical Research Commonwealth of VirginiaPart-time Clinical Research Coordinator 3; Center for Psychiatric Clinical ResearchCharlottesville, VAThe UVA Center for Psychiatric Clinical Research seeks a Clinical Research Coordinator 3. The CRC will manage the basic elements of clinical trial conduct and demonstrate a solid understanding of clinical research compliance. Prepare and submit all regulatory documentation to the IRB such as: personnel changes, annual protocol continuations, protocol modifications, adverse event reports, unanticipated events.
Grant Funded Department of Medicine Clinical Research Unit - Clinical Research Coordinator III Carilion Medical CenterGrant Funded Department of Medicine Clinical Research Unit - Clinical Research Coordinator IIIRoanoke, VirginiaR160679 Grant Funded Department of Medicine Clinical Research Unit - Clinical Research Coordinator III (Open) How You’ll Help Transform Healthcare: The Clinical Research Coordinator III manages complex clinical research studies and provides mentorship and leadership to research staff.
Clinical Research Coordinator II - Grant Funded - Cardiology Carilion Medical CenterClinical Research Coordinator II - Grant Funded - CardiologyRoanoke, VirginiaBasic responsibilities include supporting research investigators/physicians with guidance on research policies and processes, enabling successful collaborations with research sponsors, monitoring and tracking study progress, study design assistance, regulatory submission and maintenance, research subject visit management, and any other research-related duties, as necessary. Develops and maintains patient databases and study maintenance logs including but not limited to training logs, delegation of responsibility logs, screening logs, enrollment logs, and investigational product log.
Clinical Research Nurse Virginia Oncology AssociatesClinical Research NurseHampton, Virginiap style="margin:0px">***Please take this quick survey once you've submitted your resume to complete the application process: Clinical Research PI Link. Virginia Oncology Associates, the largest group of medical professionals in Hampton Roads and Northeast North Carolina devoted exclusively to cancer care and blood disorders, has an exciting opportunity for a Clinical Research RN to support our office in Hampton..
Clinical Research Coordinator Odyssey Systems Consulting Group, Ltd.Clinical Research CoordinatorPortsmouth, Virginiap style="margin:0px;text-align:left">Odyssey is proud to live out our core values of commitment, ambition, and respect in our work and communities through OdysseyCares, a philanthropic group focused on giving back through direct donations, an employer match program, and volunteering events. A minimum of two (2) years as a Clinical Research Coordinator within the past five years OR Current certification as a Certified Clinical Trial Investigator (CCTI), Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP) from the Association of Clinical Research Professionals (ACRP) or the Society of Clinical Research Associates (SoCRA).
Part-time Clinical Research Coordinator 3; Center for Psychiatric Clinical Research University of VirginiaPart-time Clinical Research Coordinator 3; Center for Psychiatric Clinical ResearchCharlottesville, VAp>You can learn more about the UVA Center for Psychiatric Clinical Research at: https://med.virginia.edu/psychiatry/research/psychiatric-clinical-research/. The UVA Center for Psychiatric Clinical Research seeks a Clinical Research Coordinator 3. The CRC will manage the basic elements of clinical trial conduct and demonstrate a solid understanding of clinical research compliance.
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.
Regulatory Clinical Research Coordinator (CRC), Licensed or Non-Licensed, varying levels Commonwealth of VirginiaRegulatory Clinical Research Coordinator (CRC), Licensed or Non-Licensed, varying levelsCharlottesville, VAThe Division of Cardiovascular Medicine (Interventional Cardiology) at the University of Virginias (UVA) School of Medicine, is currently seeking applicants for Clinical Research Coordinators (CRC), Licensed or Non-Licensed positions, at various skill and experience levels to join a dynamic growing team of clinical research professionals. This position is open to applicants who meet the requirements of Clinical Research Coordinator 2, 3 and 4. The CRC will work closely with physicians, research staff, sponsors, IRB and regulatory department staff.
NewClinical Research Coordinator I Velocity Clinical Research, Inc.Clinical Research Coordinator IHampton, VirginiaCoordinate, with supervision, assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing, and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports. Overview: Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites.
Clinical Research Coordinator - Cancer Institute at St. Francis Medical Center Bon Secours Mercy HealthClinical Research Coordinator - Cancer Institute at St. Francis Medical CenterMidlothian, VirginiaHandle consents and agreements, capture patient data and enter it into confidential data management systems provided by industry sponsors, handle regulatory (IRB) submissions for new clinical trials, submit Serious Adverse Event (SAE) information to IRBs, handle amendments, manage safety reports and submit to IRBs as appropriate, track annual review dates and submit continuing reviews, and assist with departmental needs as requested in a back-up capacity. To implement and manage aspects of all active clinical research programs and to assist in other activities as assigned by investigator providers related to these programs with responsibilities to include, but not limited to: interacting with BSHSI legal, finance, compliance, and other departments as appropriate to help start up new clinical trials.
Clinical Research Coordinator - Cancer Institute at St. Francis Medical Center Bon Secours Mercy Health IncClinical Research Coordinator - Cancer Institute at St. Francis Medical CenterVAHandle consents and agreements, capture patient data and enter it into confidential data management systems provided by industry sponsors, handle regulatory (IRB) submissions for new clinical trials, submit Serious Adverse Event (SAE) information to IRBs, handle amendments, manage safety reports and submit to IRBs as appropriate, track annual review dates and submit continuing reviews, and assist with departmental needs as requested in a back-up capacity. To implement and manage aspects of all active clinical research programs and to assist in other activities as assigned by investigator providers related to these programs with responsibilities to include, but not limited to: interacting with BSHSI legal, finance, compliance, and other departments as appropriate to help start up new clinical trials.
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.
Clinical Research Coordinator 1 - Advanced Lung Diseases Inova Health SystemClinical Research Coordinator 1 - Advanced Lung DiseasesRichmond, VAExperience screening patients for research study eligibility and collaborating effectively within multidisciplinary teams, including physicians, healthcare providers, research coordinators, and other research staff preferred. The Clinical Research Coordinator 1 - Advanced Lung Diseases implements research studies and ensures research and human subject protection within Inova from site selection to study closure.
NewClinical Research Coordinator Blue Ridge Cancer CareClinical Research CoordinatorSalem, VirginiaBusiness Experience Experience in Microsoft Office Experience working with physicians preferred Specialized Knowledge/Skills Must have excellent communication skills Excellent organizational skills Strong ability to multi-task Excellent time management skills Must have strong interpersonal skills to be able to interact with multiple people on many different levels Must have a high level of attention to detail Must be able to work in a fast-aced environment May be responsible for basic clinical assessments. Working Conditions: Environment (Office, warehouse, etc.) Traditional office environment The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job.
Regulatory Clinical Research Coordinator (CRC), Licensed or Non-Licensed, varying levels University of VirginiaRegulatory Clinical Research Coordinator (CRC), Licensed or Non-Licensed, varying levelsCharlottesville, VAp>The Division of Cardiovascular Medicine (Interventional Cardiology) at the University of Virginias (UVA) School of Medicine, is currently seeking applicants for Clinical Research Coordinators (CRC), Licensed or Non-Licensed positions, at various skill and experience levels to join a dynamic growing team of clinical research professionals. This position is open to applicants who meet the requirements of Clinical Research Coordinator 2, 3 and 4. The CRC will work closely with physicians, research staff, sponsors, IRB and regulatory department staff.
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 Coordinator US Oncology IncClinical Research CoordinatorVAp>Cookies are used on this site to assist in continually improving the candidate experience and all the interaction data we store of our visitors is anonymous. We're sorry, but it looks like this job may be no longer available or does not exist.
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.
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 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.
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-Oncology or Infusion Experience Needed-Full Time Days Mary Washington HospitalClinical Research Nurse-Oncology or Infusion Experience Needed-Full Time DaysFredericksburg, VAInstructs potential research subjects, responsible family members, and physicians, nurse practitioners, physician assistants, nursing staff, and ancillary staff involved in care of subjects on aspects of the subject's care, available clinical studies, treatments, and side effects. Essential Functions and Responsibilities: Obtains and reviews medical records for potential research subjects; maintains medical records of research subjects that include documentation of laboratory test results and progress of research study subjects, following guidelines set forth by the protocol sponsors.
Clinical Research Coordinator (Varying levels); OBGYN Commonwealth of VirginiaClinical Research Coordinator (Varying levels); OBGYNCharlottesville, VAClinical Research Coordinators will also assist with clinical trial-related activities, recruit, screen, and consent potential study participants, schedule study visits, prepare and maintain study documentation, collect data at all study visits, compile adverse event data, and manage all data collected. Clinical Research Coordinators perform a range of clinical research duties including working with research participants, processing laboratory specimens, data entry, record keeping, materials preparation, and reviewing of prospective research participants.
Clinical Research Nurse Blue Ridge Cancer CareClinical Research NurseRoanoke, VirginiaBusiness Experience Minimum 1 year of nursing experience required, preferably in oncology Experience in Microsoft Office required Experience in clinical research preferred Specialized Knowledge/Skills Ability to read, analyze, and interpret technical procedures such as protocols, informed consent documents, and regulatory documents Ability to work independently, organize, prioritize, and follow through with results Ability to solve practical problems and implement solutions Must have excellent communication skills Excellent organizational skills Strong ability to multi-task Excellent time management skills Must have strong interpersonal skills to be able to interact with multiple people on many different levels Must have a high level of attention to detail Must be able to work in a fast-paced environment May be responsible for basic clinical assessments. Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients on clinical trials.
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 Coordinator (Varying levels); Benign Gynecology Commonwealth of VirginiaClinical Research Coordinator (Varying levels); Benign GynecologyCharlottesville, VAClinical Research Coordinators will also assist with clinical trial-related activities, recruit, screen, and consent potential study participants, schedule study visits, prepare and maintain study documentation, collect data at all study visits, compile adverse event data, and manage all data collected. Clinical Research Coordinators perform a range of clinical research duties including working with research participants, processing laboratory specimens, data entry, record keeping, materials preparation, and reviewing of prospective research participants.
Clinical Research Coordinator-Varying Levels(Non-Licensed)-Cancer Center Commonwealth of VirginiaClinical Research Coordinator-Varying Levels(Non-Licensed)-Cancer CenterCharlottesville, VAp>Looking to make a meaningful impact every day The Office of Clinical Research OCR at the University of Virginia Comprehensive Cancer Center is looking for Clinical Research Coordinators Non-Licensed multiple levels to support the advancement of innovative cancer research. In this role you will help bring new therapies from research to reality by coordinating oncology clinical trials and working closely with patients physicians and multidisciplinary research teams.
Clinical Research Coordinator Alcanza Clinical Research LLCClinical Research CoordinatorCharlottesville, VAScheduling subjects for study visits and conducts appointment reminders; Building/updating source as needed; Conducting monitoring visits and resolves issues as needed in a timely manner; Ensuring study related reports and patient results are reviewed by investigator in a timely manner; Filing SAE/Deviation reports to Sponsor and IRB as needed; Documenting and reporting adverse events; Reporting non-compliance to appropriate staff in timely manner; Maintaining positive and effective communication with clients and team members; Always practicing ALCOAC principles with all documentation; May assist with study recruitment, patient enrollment, and tracking as needed; Maintaining confidentiality of patients, customers and company information, and; Performing all other duties as requested or assigned. Responsibilities may include but are not limited to: Screening of patients for study enrollment; Patient consents; Patient follow-up visits; Documenting in source clinic charts; Entering data in EDC and answers queries; Obtaining vital signs and ECGs; May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; Requesting and tracking medical record requests; Updating and maintaining logs, chart filings; Maintaining & ordering study specific supplies;].
Licensed Clinical Research Coordinator (Varying Levels); Cancer Center Commonwealth of VirginiaLicensed Clinical Research Coordinator (Varying Levels); Cancer CenterCharlottesville, VAThe Office of Clinical Research (OCR) at the University of Virginia Comprehensive Cancer Center is looking for Licensed Clinical Research Coordinators (CRC) to support the advancement of innovative cancer research. This is an excellent opportunity for detail-oriented, collaborative professionals who are passionate about high-quality research and motivated to contribute to work that improves and extends patients' lives.
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.
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 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 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 Coordin PRISM Vision GroupClinical Research CoordinFairfax, VirginiaThe company has over 250 eye care professionals and business support roles across a growing network of over 17 eye care clinic locations, spanning New Jersey, with plans to affiliate with other eye care practices in New Jersey, New York, Connecticut, Pennsylvania, Delaware, Maryland, and nationwide. Responds to requests in a timely manner, gives/receives correct information, encourages dialogue and follow-through, secures accurate signatures, maintains files in an organized and up-to-date manner.
Clinical Research Coordinators- ACORN | Family Medicine | SOM | 622750 & 622760 Commonwealth of VirginiaClinical Research Coordinators- ACORN | Family Medicine | SOM | 622750 & 622760Richmond, VAAdditionally, the Coordinators will support ACORNs quadrennial Virginia primary care evaluation, a statewide survey of all primary care practices used to assess strengths, challenges, gaps, and future directions in primary care delivery. This position requires in-person engagement with patients and clinic staff at clinical sites across Virginia, including Northern Virginia, Central Virginia, and the Tappahannock region, with the possibility of expanding to other regions of the state as needed.
Clinical Research Coordinator 1, Infectious Diseases & International Health Commonwealth of VirginiaClinical Research Coordinator 1, Infectious Diseases & International HealthCharlottesville, VAli>Assist in preparation and maintenance of existing study documentation such as: study visit schedules, study drug diaries, monitoring and or training logs, equipment records or study communications. Prepare and submit basic regulatory documentation to the Institutional Review Board (IRB) such as: personnel changes, annual protocol continuations, and minor protocol modifications.
Clinical Research Coordinator 2-4; Pediatrics Commonwealth of VirginiaClinical Research Coordinator 2-4; PediatricsCharlottesville, VAThe Department of Pediatrics in the University of Virginias UVA School of Medicine is seeking candidates for a Clinical Research Coordinator (CRC), licensed or non-licensed, at experience levels CRC 2 through CRC 4. The CRC will support clinical research efforts for the Pediatrics Department Chair as well as other divisions across the Department as needed. Demonstrate a high level of proficiency with the various electronic platforms utilized in clinical research such as IRB Pro, Protocol Builder, OnCore, iMedidata, Inform, Openclinica, Epic, and other data management platforms.
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.
Associate Director of Research and Finance Administration Eastern Virginia Medical SchoolAssociate Director of Research and Finance Administrationportsmouth, VAWorking with Strategy, Operations, and the Finance team, the AD-RFA ensures every project advances HRBRC's priorities in community engagement, data science, innovation & commercial science, and clinical/translational health research\u2014while remaining on scope, schedule, budget, and fully compliant with cross-institutional policies. By coordinating complex multi-sector proposals and overseeing post-award compliance, the role ensures the Consortium's financial health, drives sustainable growth in external funding, and delivers efficient stewardship of resources that empower scientists, community members, startups, and collaborators.
Clinical Research Coordinator, Night-shift; Emergency Medicine Commonwealth of VirginiaClinical Research Coordinator, Night-shift; Emergency MedicineCharlottesville, VAIt conducts federally funded and investigator-initiated trials in several areas of medicine, including but not limited to cardiovascular disease, pulmonary and infectious disease, status epilepticus, motor vehicle crash injury research, head injury research, and gastrointestinal-related illnesses. The Department of Emergency Medicine at the University of Virginia (UVA) School of Medicine is seeking applicants for a night-shift Clinical Research Coordinator (CRC) to join our growing team of research professionals.
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.
Associate Research Veterinarian/Research Veterinarian United TherapeuticsAssociate Research Veterinarian/Research VeterinarianBlacksburg, VirginiaToward this goal we have successfully gained FDA approval for five medicines, we are always conducting new clinical trials, and we are working to create an unlimited supply of manufactured organs for transplantation. Our public benefit purpose is to provide a brighter future for patients through (a) the development of novel pharmaceutical therapies; and (b) technologies that expand the availability of transplantable organs.
Non-licensed Clinical Research Coordinator 1; Brain Institute Commonwealth of VirginiaNon-licensed Clinical Research Coordinator 1; Brain InstituteCharlottesville, VA$25–$27 / hourPrepare and submit regulatory documentation to the IRB such as: personnel changes, annual protocol continuations, protocol modifications, adverse event reports, unanticipated events. Demonstrate proficiency with the various electronic platforms utilized in clinical research such as: IRB Pro, Protocol Builder, CRConnect, OnCore, e-regulatory platforms and Epic.
Non-licensed Clinical Research Coordinator 1, Surgery Commonwealth of VirginiaNon-licensed Clinical Research Coordinator 1, SurgeryCharlottesville, VA$25–$27 / hourThe incumbent will assist with clinical trial related activities, recruit, screen and consent potential study participants, schedule study visits, prepare and maintain study documentation, collect data at all study visits, compile adverse event data, and manage all data collected. Individuals seeking this position must have strong organization skills, have the ability to problem solve, work well in a team environment, have excellent written and oral communication skills, strong assessment skills and demonstrate an ability to learn new information quickly.