NewResearch Support Assistant 3 Schizophrenia Research 210 2026 48 Nathan S. Kline InstituteResearch Support Assistant 3 Schizophrenia Research 210 2026 48Orangeburg, NYPart timeExperience working with human research subjects• Experience with electrophysiology and MRI techniquesPreferred Qualifications:• Experience working with clinical populations and administering neuropsychological assessmentsBackground Investigation/Justice Center Review Requirements: Prospective appointees will be: 1) Checked against the Staff Exclusion List (SEL) maintained by the Justice Center for the Protection of People with Special Needs. Analyze recorded data using Matlab, EEGlab, python, and other analysis programs; perform statistical analysis of data using SPSS and Matlab; participate in scheduling experiments, and running behavioral neuropsychological experiments.
Clinical Research Coordinator - Clinical Research department in Poughkeepsie, NY Nuvance HealthClinical Research Coordinator - Clinical Research department in Poughkeepsie, NYPoughkeepsie, NY$29.65–$55.55 / hourOur 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. Performs procedures including EKG, Phlebotomy, blood and body fluid sampling, packing and shipment of human samples, body measurements and examinations within scope of practice and training, consistent with clinic and study specific policies/procedures and scope of care under the guidance of the supervisor.
Research Support Assistant II - Center for Dementia Research Nathan S. Kline InstituteResearch Support Assistant II - Center for Dementia ResearchOrangeburg, NYFull timeJOB QUALIFICATIONS:Minimum Qualifications:• BS in Neuroscience• Previous research experience• Previous experience with immunohistochemistry• Experience with GraphPad Prism• Experience with poster presentationPreferred Qualifications:• Cell culture experience preferred• Some experience with Western Blot• Experience handling small laboratory animals preferredBackground Investigation/Justice Center Review Requirements: Prospective appointees will be: 1) Checked against the Staff Exclusion List (SEL) maintained by the Justice Center for the Protection of People with Special Needs. Prospective employees whose names appear on the SEL as having been found responsible for serious or repeated acts of abuse or neglect will be barred from appointment.
Research Scientist 4 - MRI, Nathan S. Kline Research Institute, P27763 New York State Thruway AuthorityResearch Scientist 4 - MRI, Nathan S. Kline Research Institute, P27763Orangeburg, NY$106,898–$131,665 / yearIf appointed you may be required to become an enrolled Medicare provider; obtain and provide to your employer a National Provider Identifier (NPI) number issued by the National Plan and Provider Enumeration System (NPPES); and otherwise actively participate to the degree necessary to allow for your services to be billed through Medicare and Medicaid. This individual will play a central role in supporting high-quality neuroimaging on our research MRI platform, contributing to scientific discovery, operational excellence, participant care, and the advancement of imaging capabilities across the Institute.
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 Project Manager iMPact Business GroupClinical Research Project ManagerMahwah, NJLeading people who perform project management duties involving cross-functional teams focused on delivering internal products or administrative systems. Organizing project activities and interdepartmental meetings, ensuring communication facilitates the completion of the program or project on schedule and within budget constraints.
Research Scientist I - C-BIN Nathan S. Kline InstituteResearch Scientist I - C-BINOrangeburg, NYFull timeD. in neuroscience, cognitive neuroscience, psychology, biomedical engineering, computer science, or a related field• Strong background in human memory research, cognitive neuroscience, or a closely related area demonstrated by track-record of publications• Demonstrated ability to independently develop and execute novel analysis approaches on complex datasets• Scientific programming experience (e.g., Python, MATLAB, R)• Strong written and oral communication skills• Demonstrated expertise in advanced fMRI analysis approaches, including but not limited to multivoxel pattern analysis, temporal dynamics, functional connectivity• Experience with Transcranial Magnetic Stimulation (TMS) or other noninvasive human brain stimulation methods• Familiarity with multimodal data integration approaches, EEG and/or physiological data collection and/or analysis• Experience mentoring junior researchersBackground Investigation/Justice Center Review Requirements: Prospective appointees will be: 1) Checked against the Staff Exclusion List (SEL) maintained by the Justice Center for the Protection of People with Special Needs. JOB DUTIES:- Work both independently and collaboratively, taking ownership of analysis projects while contributing to a team-oriented research environment- Contribute to the conceptual design and implementation of NIH-funded studies on awake memory consolidation- Oversee data quality monitoring and preprocessing of fMRI, physiology, and behavioral data- Develop and execute novel, advanced data analysis projects on prospective and existing datasets with collaborative input- Drive manuscript preparation and publication of research findings- Mentor Research Assistants on data collection protocols and analysis projects- Participate in lab meetings and contribute to the broader intellectual life of the research group- Present research findings at national and international conferencesJOB QUALIFICATIONS:Minimum Qualifications:Bachelor's degree and two years of professional research in an appropriate field or master's degree in an appropriate field may substitute for one year of the experience.
NewSpec 3, Clinical Research MillenniumSoft IncSpec 3, Clinical ResearchFranklin Lakes, NJWorks with many different disciplines (manufacturing, marketing, quality, regulatory, etc.), materials, products and processes in the development of core clinical laboratory and outside the core clinical laboratory products and services. Proven understanding of clinical laboratory testing, blood collection, Urinalysis, POC and LIS/LIMS systems and an ability to apply knowledge to innovative concepts/projects beyond the core clinical laboratory.
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 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.
Principal Business Analyst - Research Program Management Regeneron PharmaceuticalsPrincipal Business Analyst - Research Program ManagementTarrytown, NY$114,800–$187,400 / yearBuild our future together: The Principal Business Analyst Research Program Management (RPM), will work collaboratively with Research Program Managers, Research & Preclinical Development scientists, as well as other IT stakeholders, to understand and document scientific drug discovery and data processes and translate these into requirements for the development of data and technology solutions that support Regeneron's scientific mission. We need someone who is adept at using a variety of tools (e.g., Laboratory Information Management Systems, SQL databases, data and process modeling frameworks) in order to perform business analysis, elicit and document requirements, map data flows, and drive data quality improvements in a research-focused environment.
Medical Technologist 1 (NY HELPS), Nathan Kline Research Institute, P27764 New York State Thruway AuthorityMedical Technologist 1 (NY HELPS), Nathan Kline Research Institute, P27764Orangeburg, NY$53,764–$68,630 / yearMinimum of 90 semester hours or equivalent in an accredited college or university and the successful completion of a course of training of at least 12 months in a school of medical technology approved by the Council on Medical Education of the American Medical Association. Any combination of academic study and training and/or experience outlined in Section 58 of Title 10 of the New York State Public Health Law as referenced in the New York State Codes, Rules, and Regulations (NYCRR).
Senior Research Specialist - Tpk/Pd Regeneron PharmaceuticalsSenior Research Specialist - Tpk/PdTarrytown, NY$93,900–$153,300 / yearThis person will contribute to PK/TK protocol design/input, support CRO studies, produce Pharmacometrics deliverables and regulatory tables/figures/listings, and follow all SOPs to ensure GxP/GLP compliance. Independently executes a broad array of work supporting department priorities in routine Pharmacometrics deliverables on study design, analysis, and reporting.
Senior Research Specialist - TPK/PD Regeneron Pharmaceuticals IncSenior Research Specialist - TPK/PDtarrytown, NY$93,900–$153,300 / yearThis person will contribute to PK/TK protocol design/input, support CRO studies, produce Pharmacometrics deliverables and regulatory tables/figures/listings, and follow all SOPs to ensure GxP/GLP compliance. Independently executes a broad array of work supporting department priorities in routine Pharmacometrics deliverables on study design, analysis, and reporting.
NewResearch & Development Rotational Program Associate PfizerResearch & Development Rotational Program AssociatePearl River, NY$60,200–$100,400 / yearThis in-depth skills development and experiential program offers graduates the opportunity to gain experience and insight into drug discovery and development from leading scientists, clinicians, statisticians, epidemiologists and professionals, and to bridge from student to industry professional, or into an advanced-degree program. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.
Senior Clinical Study Manager (Hybrid) StrykerSenior Clinical Study Manager (Hybrid)Mahwah, New JerseyAs Senior Clinical Study Manager, you will serve as the cross-functional project leader responsible for delivering clinical research business initiatives through effective project execution, stakeholder engagement, process improvement, technology implementation, and compliance-focused operational support. Experience implementing or optimizing clinical technology platforms such as clinical trial management systems, electronic data capture systems, electronic trial master files, electronic clinical outcome assessment tools, analytics, reporting, or quality management systems.
NewSummer 2027 Internship - Clinical Affairs - New Jersey StrykerSummer 2027 Internship - Clinical Affairs - New JerseyMahwah, New JerseyAs a Clinical Affairs intern at Stryker, you will: Work cross functionally with different departments including R&D Engineering, Project Management, Health Care Solutions, Marketing, and Regulatory Affairs to assist in clinical research programs and develop a broad understanding of the regulated clinical research landscape. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.
Development Head, Rsv, RSV Combination, And Early Vaccine Programs PfizerDevelopment Head, Rsv, RSV Combination, And Early Vaccine ProgramsPearl River, NY$330,200–$550,400 / yearApplies technical/scientific expertise to resolve issues regarding the clinical components of documents (e.g., Investigational New Drugs, New Drug Applications/Common Technical Documents, global registration dossiers, lifecycle strategy documents, internal documents). Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.
Development Head, RSV, RSV Combination, and Early Vaccine Programs PfizerDevelopment Head, RSV, RSV Combination, and Early Vaccine ProgramsPearl River, New York$330,200–$550,400 / yearApplies technical/scientific expertise to resolve issues regarding the clinical components of documents (e.g., Investigational New Drugs, New Drug Applications/Common Technical Documents, global registration dossiers, lifecycle strategy documents, internal documents). Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.
Clinical Development Medical Director Pfizer IncClinical Development Medical DirectorPearl River, NY$239,900–$399,800 / yearSupport study team: Provides clinical input to protocol/study team for monitoring guidelines, statistics analysis plans, ICDs, clinical review forms, data edit checks, data quality planning, as needed (ultimately oversees work of protocol/study team). Proven experience in the pharmaceutical industry (biopharmaceutical industry or Clinical Research Organization) related to clinical research programs and registration activities, preferably for vaccines, or; An investigator with significant experience in vaccine clinical studies in academic, NGO or public health institutions may be considered.