NewClinical Research Budget Manager, Office of Research and Project Administration Memorial Sloan Kettering Cancer CenterClinical Research Budget Manager, Office of Research and Project AdministrationNew York, New YorkRemoteInformed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of cancer as a disease and improving the ability to prevent, diagnose, and treat it. 2-4 years in clinical research financial management, including budget development, Medicare coverage analysis, clinical trial agreements, invoicing, and fiscal management.
Market Research Group Research Director - Quantitative Lieberman IncMarket Research Group Research Director - QuantitativeGreat Neck, NYRemoteAbout You We are looking for a seasoned market research professional who brings: Bachelors degree in a related field such as Market Research, Psychology, Sociology, Economics, Business, Industrial Psychology, or a similar discipline 7+ years of quantitative market research experience Pharmaceutical industry research experience preferred Advanced proficiency in Microsoft Office applications, including Excel, Word, and PowerPoint, as well as SPSS Exceptional written and verbal communication skills Strong attention to detail and commitment to quality Proven ability to build and maintain relationships with clients and internal stakeholders. Strong leadership skills with experience managing and developing high-performing teams Exceptional organizational and project management abilities Proven capacity to manage multiple priorities, projects, and teams in a fast-paced environment Strategic thinker with strong analytical and problem-solving skills Collaborative and client-focused approach Commitment to delivering excellence and driving meaningful business outcomes.
Senior Clinical Research Associate Zp Group LlcSenior Clinical Research AssociateNYRemote$155,000–$175,000 / yearKeywords: clinical research, clinical trials, CRA, general medicine, GCP, ICH, regulatory compliance, site monitoring, CTMS, EDC, protocol training, clinical documentation, data review, query resolution, clinical operations, FDA regulations, SOPs, quality oversight, risk-based monitoring, therapeutic areas. The Senior Clinical Research Associate (CRA) will join a remote, contract-based team supporting Phase II and Phase III studies across a variety of general medicine indications within a full-service clinical research environment.
Customer Service Representative-Clinical (Remote- $15/hr) Remote, United States American Specialty Health IncCustomer Service Representative-Clinical (Remote- $15/hr) Remote, United StatesNYRemoteHowever, 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 Company's legal duty to furnish information. This WFH position requires you have a stable connection to your Internet Service Provider with the ability to participate by video in online meetings over a reliable and consistent network.
Clinical Research Associate Actalent IncClinical Research AssociateNewark, NJRemote$85–$90 / hourIf you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. The role offers a weekly workload of 40-50 hours, varying by study phase, with opportunities for hybrid work arrangements to support work-life balance.
Research Partner Success Manager Helix OpCo LLCResearch Partner Success ManagerNYRemote$106,000–$148,000 / yearOur clinico-genomic dataset includes clinical and Exome+ sequencing data and is curated to facilitate the discovery of novel genomic disease risks, enhance patient recruitment for clinical studies, support clinical decision-making, and optimize care pathways. The Helix Clinico-genomic Data Team plays a pivotal role in Helix's efforts to provide a first-in-class clinico-genomics research dataset for our partners to conduct and publish cutting-edge genomic studies.
Insurance Coverage Attorney - NYC/Westchester (Valhalla) / (hybrid office/remote) (Remote) Kaufman Borgeest & RyanInsurance Coverage Attorney - NYC/Westchester (Valhalla) / (hybrid office/remote) (Remote)New York, NYRemote$105,000–$200,000 / yearThis position is for an attorney with 0+ years' experience to join the Insurance Coverage/Coverage Litigation teams in our New York City or Westchester offices, who represent international and domestic insurers in complex insurance and coverage litigation matters involving all manner of liability policies, including Management Liability (D&O, EPL, Fiduciary, Crime), Cyber, Professional Liability, Financial Institutions, and Commercial General Liability. Strong legal research, writing and verbal communication skills; Ability to interact with clients and command client confidence; Ability to manage and prioritize multiple projects; Excellent organizational and time management skills; Ability to identify and resolve problems quickly.
Staff Consultant, Research Komodo Health IncStaff Consultant, ResearchNYRemote$160,000–$195,000 / yearWe work at the intersection of clinical science, data analytics, and client strategy - increasingly powered by AI that lets us pair speed with quality, moving from data to decision faster than ever without compromising rigor, while collaborating closely with cross-functional teams to deliver impactful solutions to the industry''s most pressing challenges. The Senior Research Consulting Manager is both a rigorous analytic lead and a trusted advisor to clients: someone equally comfortable designing a study, defending a methodology, and sitting across the table from a client stakeholder to translate findings into action.
FSP Sr. Clinical Research Associate II - NYC Metro or PHL - Onc Fortrea IncFSP Sr. Clinical Research Associate II - NYC Metro or PHL - OncNew York, NYRemote$125,000–$140,000 / yearResponsibilities: Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.
Hiring Remote Insurance Brokers (Remote) The Edelson AgencyHiring Remote Insurance Brokers (Remote)Newark, NJRemoteResponsibilities include assessing client needs, recommending policies, managing applications, and providing ongoing support with claims and renewals. We are Seeking a motivated Insurance Broker to help clients find the right insurance coverage.
NewSenior Clinical Study Manager - Remote Penfield Search PartnersSenior Clinical Study Manager - RemoteFairfield, CTRemoteClinical Study Manager role is responsible for managing the overall clinical operations of pre-clinical and clinical diagnostic trials, including study planning, budgeting, resource management, and, when applicable, oversight of contract research organizations (CROs). Develop and maintain effective communication across functions, including Executive/Leadership, Research & Development, Medical Affairs, Scientific Affairs, Regulatory Affairs, Finance, and Commercial teams.
Clinical Research Associate Alto Neuroscience IncClinical Research AssociateNYRemote$80,000–$125,000 / yearDetermine whether all adverse events (AEs) are appropriately reported within the time periods required by GCP, the protocol, the Ethic Committees (IRB/IEC), Sponsor and the applicable regulatory requirement(s) Ensure deviations from the protocol, SOPs, GCP, and the applicable regulatory requirements are documented and communicated appropriately and take appropriate action to prevent recurrence of the detected deviations. The Clinical Research Associate (CRA) is responsible for the oversight of assigned investigative sites in accordance with all applicable protocols, project plans, Sponsor SOPs, GCP guidelines, and regulatory requirements from site initiation through site close out.
Key Account Director, Diagnostics And Research TempusKey Account Director, Diagnostics And ResearchNew York, NYRemote$150,000–$200,000 / yearThe diagnostic (Dx) segment of the Tempus Precision Medicine Platform-which includes sequencing diagnostics, companion diagnostics (CDx) development, multiomics, and CRO partnerships-is central to the future of scalable drug development and the broader realization of personalized medicine. Align the cross functional team of Product Specialists, partner Key Account Directors (KADs), Translational Researchers and Commercial Operations to most efficiently identify and deliver value at our clients.
Key Account Director, Diagnostics and Research Tempus AI IncKey Account Director, Diagnostics and ResearchNYRemote$150,000–$200,000 / yearThe diagnostic (Dx) segment of the Tempus Precision Medicine Platform-which includes sequencing diagnostics, companion diagnostics (CDx) development, multiomics, and CRO partnerships-is central to the future of scalable drug development and the broader realization of personalized medicine. Align the cross functional team of Product Specialists, partner Key Account Directors (KADs), Translational Researchers and Commercial Operations to most efficiently identify and deliver value at our clients.
Director, Medical Science Liaison - Infectious Disease & Immunology (IDI) Remote Quest Diagnostics IncDirector, Medical Science Liaison - Infectious Disease & Immunology (IDI) RemoteSecaucus, NJRemote$140,000–$185,000 / yearParticipate in key scientific and medical conferences to serve as medical liaison for Quest Diagnostics at scientific booth (when appropriate), present relevant scientific research, collaborate with Public Relations team on data dissemination, and meet with key TL to identify collaborative opportunities. TLs may include nationally, regionally, and locally recognized scientific and clinical leaders, medical advisors to managed care providers and committees, payers, and HCPs active in addressing patient advocacy issues.
Clinical Research Scientist II Spring Care IncClinical Research Scientist IINYRemote$120,000–$140,000 / yearWith outcomes independently validated by JAMA Network Open and the Validation Institute, Spring Health reaches more than 170 million people worldwide through leading employers, health plans, and partners. You will work closely with scientists and cross-functional partners, with guidance and support from research leadership on study operations, prioritization, risk management, and complex program decisions.
Data Scientist - Clinical Analytics (Remote) Penfield Search PartnersData Scientist - Clinical Analytics (Remote)Fairfield, CTRemoteThe ideal candidate combines strong programming and technical development skills with an understanding of clinical studies and the ability to build practical solutions that improve how teams access, analyze, visualize, and work with clinical data. Strong cross-functional communication skills with the ability to work effectively across Biostatistics, Statistical Programming, Data Management, and other clinical functions.
Remote Registered Dietitian or CNS - Flexible Hours, Work from Anywhere Berry StreetRemote Registered Dietitian or CNS - Flexible Hours, Work from AnywhereBrooklyn, NYRemoteBerry Street empowers independent dietitians to accept insurance and grow thriving private practices by providing comprehensive credentialing, scheduling, referral, and technical support, as well as access to a vibrant, collaborative clinician community. Dietitians working with Berry Street are committed to these pillars of high-quality care: Evidence-based: We provide quality care based on the latest clinical research.
Director of the Office of Research Compliance Monmouth UniversityDirector of the Office of Research ComplianceWest Long Branch, New JerseyRemote$128,000–$140,000 / yearThe Director provides direction and administrative oversight to all core components of the institution’s Human Research Protection Program (HRPP), the Institutional Review Board (IRB), the Institutional Animal Care and Use Committee (IACUC), institutional biosafety, research misconduct, conflict of interests, data privacy and security requirements, responsible conduct of research, research security and foreign influence, and export controls. Plan, direct, and oversee research and compliance operations for the University, including, but not limited to the Institutional Review Board for Human Subjects (IRB), the Institutional Animal Care and Use Committee (IACUC), institutional biosafety, financial conflict of interest management (institutional, financial, and individual), data privacy and security requirements, responsible conduct of research, security and foreign influence, research misconduct, and export controls.
Director Of The Office Of Research Compliance Monmouth UniversityDirector Of The Office Of Research ComplianceWest Long Branch, NJRemote$128,000–$140,000 / yearThe Director provides direction and administrative oversight to all core components of the institution's Human Research Protection Program (HRPP), the Institutional Review Board (IRB), the Institutional Animal Care and Use Committee (IACUC), institutional biosafety, research misconduct, conflict of interests, data privacy and security requirements, responsible conduct of research, research security and foreign influence, and export controls. Duties and Responsibilities: Plan, direct, and oversee research and compliance operations for the University, including, but not limited to the Institutional Review Board for Human Subjects (IRB), the Institutional Animal Care and Use Committee (IACUC), institutional biosafety, financial conflict of interest management (institutional, financial, and individual), data privacy and security requirements, responsible conduct of research, security and foreign influence, research misconduct, and export controls.