Clinical Research Coordinator Hackensack University Medical CenterClinical Research CoordinatorParamus, NJA day in the life of a Clinical Research Coordinator at Hackensack Meridian Health includes: Acts as liaison between principal investigators, sub-investigators, clinical research nurses and regulatory specialists on all regulatory issues and changes within the protocol. Schedules, coordinates, prepares, and assists for all sponsor monitor site visits and ensures all supporting documentation records are adequate and available for the visit; Meets with monitor at least once during each monitor site visit and resolves all issues found during visit.
Clinical Research Assistant Stony Brook UniversityClinical Research AssistantStony Brook, NYBrief Description of Duties: The Clinical Research Assistant participates in enrolling human subjects into research protocols by performing informed consent process with potential study subjects, explaining protocols, answering questions, and fulfilling regulatory requirements for informed consent form; maintains consent forms; schedules visits, coordinates subject follow-up; in both the Infectious Diseases Clinic at Stony Brook University or research sites. In lieu of a Bachelor''s degree and One (1) year of full-time experience working in a patient-related research environment, an Associate's degree (foreign equivalent or higher) and Three (3) years of full-time experience working in a patient-related research environment may be considered.
Clinical Research Associate, Sponsor Dedicated IQVIA Holdings IncClinical Research Associate, Sponsor DedicatedNew City, NY$71,900–$189,000 / yearEnsure 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 Coordinator Lead Nuvance HealthClinical Research Coordinator LeadPoughkeepsie, NY$33.21–$61.68 / hourEvaluates trial protocols, manages the clinical research sites including, but not limited to acting as primary contact for clinical research sites for questions related to the protocol conduct protocol, regulatory document completion, study supplies, client scheduling, and electronic data capture. Our team of more than 15,000 caregivers delivers compassionate care through seven community hospitals, primary care and specialty practice locations, outpatient settings, home care services and telehealth visits.
Clinical Research Nurse Hackensack University Medical CenterClinical Research NurseParamus, NJA day in the life of a Clinical Research Nurse at Hackensack Meridian Health includes: Assists the principal investigator in the preparation of proposed clinical trials by reviewing trial protocol, contacting each department who will provide resources during study and ensuring appropriate departments are notified and given a copy of proposed trial, scientific merit and accrual potential. The Clinical Research Nurse is responsible for coordinating and overseeing clinical research operations for all assigned clinical trials and participates in assessing, planning, implementing and evaluating Compliant Patient Care in clinical research trials.
Clinical Research Nurse 1 Yale UniversityClinical Research Nurse 1New Haven, CT$65,000–$101,000 / year3. Contributes to protocol development, submission, and renewal by collecting written materials and writing procedural documents; ensures ongoing compliance with institutional review board (IRB) policies by monitoring changes in IRB policies related to human specimens and informing the research team of such changes. Contributes to protocol development, submission, and renewal by collecting written materials and writing procedural documents; ensures ongoing compliance with institutional review board (IRB) policies by monitoring changes in IRB policies related to human specimens and informing the research team of such changes.
Clinical Research RN - Oncology - Per Diem Hackensack University Medical CenterClinical Research RN - Oncology - Per DiemHackensack, NJAssists the principal investigator in the preparation of proposed clinical trials by reviewing trial protocol, contacting each department who will provide resources during study and ensuring appropriate departments are notified and given a copy of proposed trial, scientific merit and accrual potential. The Clinical Research Nurse is responsible for coordinating and overseeing clinical research operations for all assigned clinical trials and participates in assessing, planning, implementing and evaluating Compliant Patient Care in clinical research trials.
Clinical Research Analyst Yale UniversityClinical Research AnalystNew Haven, CT$55,000–$85,000 / yearActivities supported by regulatory affairs include, but may not be limited to: preparation and submission of initial protocol, amendment, and continuing review submissions to the Protocol Review Committee, IRB, and ancillary committees; tracking evidence of protocol and IRB-required training for all research staff; maintenance and sharing of regulatory files with study sponsor monitors, auditors and inspectors to ensure compliance with protocol requirements, university and applicable authorities; receipt and tracking of safety reports; collaborating with CTO staff, laboratory and pharmacy staff regarding study status changes; and serving as a liaison between the CTO, research staff and study sponsor when communicating regulatory matters. Works closely with investigators and other study team members including the project manager, for projects or programs of a small size or sections of medium projects and programs to consult, conduct analysis, and identify trial objectives and requirements within specific parameters.
Clinician & Clinical Research Director (Ccrd) Yale UniversityClinician & Clinical Research Director (Ccrd)New Haven, CT$105,000–$174,000 / yearIn conjunction with the Principal Investigator, the CCRD will provide oversight of all programmatic activities and staff including, but not limited to, the following: Provide senior clinical, operational, administrative, and strategic leadership for multidisciplinary clinical research and healthcare delivery programs supporting Yale research initiatives in conjunction with the Principal Investigator. The CCRD serves in a senior leadership capacity across clinical, administrative, research, and policy domains and is responsible for strategic growth planning, program expansion into additional clinical and community settings, workforce development, and implementation of scalable and sustainable clinical research operations in conjunction with the Principal Investigator.
YCCI Manager, Clinical Research Billing Compliance Yale UniversityYCCI Manager, Clinical Research Billing ComplianceNew Haven, CT$82,000–$131,500 / yearThis includes leading, managing, and advising on the following: departmental and cross-departmental initiatives, projects, and requests for assistance by the University community; delivery of day-to-day service levels, customer experience, and billing compliance; change management within the billing compliance department in accordance with changes to laws and regulation governing the topic; collaborations with other business units; operational effectiveness and strategies to ensure quality and efficiency; operational opportunities, risk management, continuous quality improvement; and verifying that institutional requirements have been satisfied. This includes leading, managing, and advising on the following: clinical research billing compliance activities (e.g., Physician and Hospital Billing charge review, clinical research billing audits, Clinical Trial Management System (OnCore) patient billing plan set up and execution, research billing audits, etc.), systemic reviews to evaluate billing compliance to ensure compliance with all federal, state and local laws and regulations governing research billing compliance, responding to patient billing inquiries.
Ycci Manager, Clinical Research Billing Compliance Yale UniversityYcci Manager, Clinical Research Billing ComplianceNew Haven, CT$82,000–$131,500 / yearThis includes leading, managing, and advising on the following: departmental and cross-departmental initiatives, projects, and requests for assistance by the University community; delivery of day-to-day service levels, customer experience, and billing compliance; change management within the billing compliance department in accordance with changes to laws and regulation governing the topic; collaborations with other business units; operational effectiveness and strategies to ensure quality and efficiency; operational opportunities, risk management, continuous quality improvement; and verifying that institutional requirements have been satisfied. This includes leading, managing, and advising on the following: clinical research billing compliance activities (e.g., Physician and Hospital Billing charge review, clinical research billing audits, Clinical Trial Management System (OnCore) patient billing plan set up and execution, research billing audits, etc.), systemic reviews to evaluate billing compliance to ensure compliance with all federal, state and local laws and regulations governing research billing compliance, responding to patient billing inquiries.
Clinician & Clinical Research Director (CCRD) Yale UniversityClinician & Clinical Research Director (CCRD)New Haven, CT$105,000–$174,000 / yearIn conjunction with the Principal Investigator, the CCRD will provide oversight of all programmatic activities and staff including, but not limited to, the following: Provide senior clinical, operational, administrative, and strategic leadership for multidisciplinary clinical research and healthcare delivery programs supporting Yale research initiatives in conjunction with the Principal Investigator. The CCRD serves in a senior leadership capacity across clinical, administrative, research, and policy domains and is responsible for strategic growth planning, program expansion into additional clinical and community settings, workforce development, and implementation of scalable and sustainable clinical research operations in conjunction with the Principal Investigator.
Senior Clinical Research Associate Trevi Therapeutics IncSenior Clinical Research AssociateNew Haven, CTFor a description, see PDF: https://trevitherapeutics.com/wp-content/uploads/2026/09/Senior_CRA_JD-Rv09.2026.pdf .
Clinical Research Coordinator U.S. Renal Care, Inc.Clinical Research CoordinatorOrange, Connecticut$73,593–$91,992 / yearFull timeClinical Research Coordinator (SCRC), the clinical site, sponsor(s), clinical research organization(s) (CROs), institutional review boards (IRBs), and study participants to ensure Execution of the clinical trial in accordance with the Study Protocol, the Food and Drug Administration (FDA), International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) and applicable state and local regulations. (Including but not limited to: Form FDA 1572, financial disclosures, laboratory certifications, protocol, investigator brochure, institutional review board (IRB) related documents, IND reports delegation of authority (DOA), study specific enrollment logs, monitoring reports, with assistance as needed.
Research And Clinical Services Librarian Yale UniversityResearch And Clinical Services LibrarianNew Haven, CT$68,000–$145,250 / yearReporting to the Associate Director for Research and Scholarly Services, the Research and Clinical Services Librarian leads the law library's dynamic and proactive research, instructional, and reference support to faculty, students, and staff in Yale Law School's expansive clinical program. As a member of the Research and Instructional Services team, the Research and Clinical Services Librarian participates in the faculty liaison program, staffs the reference desk, conducts research consultations, and contributes to the library's instructional program.
Research and Clinical Services Librarian Yale UniversityResearch and Clinical Services LibrarianNew Haven, CT$68,000–$145,250 / yearReporting to the Associate Director for Research and Scholarly Services, the Research and Clinical Services Librarian leads the law library's dynamic and proactive research, instructional, and reference support to faculty, students, and staff in Yale Law School's expansive clinical program. As a member of the Research and Instructional Services team, the Research and Clinical Services Librarian participates in the faculty liaison program, staffs the reference desk, conducts research consultations, and contributes to the library's instructional program.
Clinical Research Coordinator The Geneva FoundationClinical Research CoordinatorWest Point, New YorkHeadquartered at the Uniformed Services University of the Health Sciences (USU), MIRROR provides coordination and support of inter-service and inter-disciplinary partnerships across military treatment facilities (MTFs), military training centers (MTCs), and civilian academic centers to execute cutting-edge research in order to mitigate the burden of MSI on military readiness. Maintain and update files of all applicable regulatory documentation for IACUC or IRB (including protocols, approvals, amendments, modifications, etc.) as well as any communications with the sponsor or any other Federal or regulatory office (including prior approvals, change in scope, etc.).
Clinical Research Coordinator New York Medical CollegeClinical Research CoordinatorHawthorne, New YorkFull timeOverview: The Division of Medical Genetics at New York Medical College is seeking a clinical research coordinator to work with our team on multiple clinical trials. Must be adept at keeping track of multiple projects, able to work independently, and have strong problem solving, communication, and analytical skills.
RN Clinical Research Hartford HealthCare CorpRN Clinical ResearchFairfield, CTIn compliance with all regulatory, institutional and departmental requirements, performs patient screening, data collection and data entry for research protocols, databases and projects within Hartford Healthcare Cancer Institute, and ensures the data quality and integrity for each clinical trial. Coordinate and conduct the operation of clinical trials as per GCP and ICH guidelines including participant recruitment; informed consent; continuous monitoring of protocol for compliance and patient safety; source document review; data entry; sponsor monitoring.
Manager, Oncology Clinical Research Operations Hartford HealthCare CorpManager, Oncology Clinical Research OperationsFairfield, CTManager, Oncology Clinical Research Operations is responsible for managing a team of Clinical Research Coordinators (CRCs) and research nurses ensuring the efficient and compliant execution of all oncology clinical trials within a region of Hartford HealthCare. Operational Oversight: Guide the delivery of a trial, including support for start-up, enrollment management, site engagement, monitoring planning and execution, regulatory documentation, data cleaning activities, and close-out.