Project Manager, Contracts & Operations Lupus Research Alliance Inc.Project Manager, Contracts & OperationsNew York, NY$75,000–$85,000In 2018, the LRA established a clinical affiliate organization, Lupus Therapeutics (LT), which is responsible for the coordination, conduct and management of a North American-based clinical trial network, the Lupus Clinical Investigators Network (LuCIN), as well as Patient Engagement and Equity efforts to foster clinical research for the development of new therapies and clinical care approaches for the diverse lupus community. This position blends project management — planning, tracking, and driving initiatives to completion — with contract administration, including preparing agreements and invoices; tracking and monitoring agreements with biopharmaceutical and biotech partners, vendors, individuals living with lupus,, study sites, and member organizations.
Senior Medical Director, Clinical Development Spyre Therapeutics IncSenior Medical Director, Clinical DevelopmentNY$343,000–$365,000 / yearThe Senior Director will play a pivotal role as a key clinical contributor within our global clinical development programs, partnering with cross-functional teams to support the design, planning, and implementation of study protocols and regulatory activities that advance the development of our cutting-edge antibody portfolio. We also embrace differences in experience and background, and welcome diversity of opinions and thought with active recruitment designed to create a stronger and better Spyre that is focused on developing life-changing products for patients.
Clinical Data Scientist/ Methodologist SanofiClinical Data Scientist/ MethodologistBridgewater, NJ$100.50–$145.17 / hourMinimum 4-5 years for Master's degree holder or 2-4 years for Doctoral degree holder of relevant experience in real-world data, commercial analytics, real-world evidence, health outcomes research, fit-for-purpose feasibility assessment, data quality assessment or a related field within the pharmaceutical, biotech, or health technology industry. This role serves as a methodological authority and RWD data domain expert, ensuring best-in-class data selection and optimal data usage to generating reliable insights or evidence to better understanding gaps in patient care and healthcare providers involved in patient care.
Clinical Supply Chain Project Leader SanofiClinical Supply Chain Project LeaderMorristown, NJ$105–$151.67 / hourThe CSC-PL will also ensure clear, concise, consistent, and timely communication with stakeholders and act as a change agent through the leadership of global initiatives targeting process improvement and engaging all partners throughout the clinical supply chain. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen.
NewDirector, Clinical Testing & Claims, R&D e.l.f. BeautyDirector, Clinical Testing & Claims, R&DNew York, New YorkAdditionally, the role identifies the latest ingredient technologies and actively mines for innovative ingredients to drive pipeline innovation; monitors competitive claims and stays current on emerging research across skin, color, and hair; and partners closely with our global R&D formulation team and Product Development to share insights, methods, and technologies that inform development and positioning. This Director establishes fit‑for‑purpose study protocols and designs that demonstrate efficacy and enable compelling, including numerical, claims; manages all testing details and key milestones to meet timelines; and builds strategic relationships with external labs to optimize timing, quality, and cost.
Senior Director, Regional Clinical Study Management BeOne Medicines AGSenior Director, Regional Clinical Study ManagementNY$206,200–$276,200 / yearGeneral Description: As part of the regional leadership team, provides inspirational leadership, proactive management, and feedback-oriented mentorship to clinical study managers at various levels for assigned portfolio and may lead a designated therapeutic area or asset. Shapes and influences strategies to ensure that the clinical studies are operationally feasible in the region, optimizes trial feasibility, country allocation and site selection process for assigned region in collaboration with feasibility managers, country heads, medical affairs and any other stakeholders.
MR Clinical Education Specialist (Northeast/Midwest/and Central) Varian Medical Systems IncMR Clinical Education Specialist (Northeast/Midwest/and Central)NY$89,220–$122,672 / yearIt is Siemens Healthineers' policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations.". In this role you will ensure that the Clinical Education training on Siemens MR Imaging systems and components are facilitated to provide expert technical training, deliver customer excellence, and represent Siemens Healthineers and Clinical Education with professionalism and a focus on delivering a positive customer experience.
NewSenior Manager R&D Quality Analytics & Portfolio Insights BeOne Medicines AGSenior Manager R&D Quality Analytics & Portfolio InsightsNY$136,500–$181,500 / yearThese may include statistical monitoring, predictive risk models, anomaly-detection methods, patient-safety and adverse-event reporting analytics, data-informed audit packages, risk indicators, dashboards, automated monitoring, natural-language tools, and other scalable capabilities that support Quality by Design, Risk-Based Quality Management, audit and inspection readiness, vendor, process, and system oversight, and targeted risk mitigation. Develop analytical approaches to support data-informed audit planning/execution and identify potential patient-safety and subject-protection risks, including adverse-event under-reporting or over-reporting, unusual clinical-event patterns, protocol-compliance concerns, data-quality issues, and other signals requiring targeted Quality review.
Medical Affairs Manager Beauty Health Group LimitedMedical Affairs ManagerNYRemote$121,000–$145,000 / yearPartner cross-functionally with Research & Development, Regulatory Affairs, Quality, Marketing, Clinical Operations, Legal, and Commercial teams to provide scientific guidance that supports product development, commercialization, educational initiatives, and business strategy. Build and maintain productive relationships with Key Opinion Leaders (KOLs), investigators, research partners, and advisory board members to gather external insights, support innovation, and strengthen scientific collaborations.
NewAssociate Director, Clinical Client Services Capital Rx LLCAssociate Director, Clinical Client ServicesNew York, NY$160,000–$190,000 / yearJudi Health is an enterprise health technology company providing a comprehensive suite of solutions for employers and health plans, including: Judi Rx, a public benefit corporation delivering full-service pharmacy benefit management (PBM) solutions to self-insured employers, Judi Health, which offers full-service health benefit management solutions to employers, TPAs, and health plans, and. Partner with Account Executives and Sales to support strategic client planning, reviews, renewals, finalist presentations, and key client discussions.
NewResearch Business Specialist Hackensack Meridian HealthResearch Business SpecialistClifton, New JerseyFull timeThe Research Business Specialist provides support to Hackensack Meridian Health, Office of Research Administration, for pre/post award financial management of Clinical Trial research and ongoing support for the management of the Oncore Clinical Trial Management System (CTMS) across the HMH Network. The posted rate of pay in this job posting is a reasonable good faith estimate of the minimum base pay for this role at the time of posting in accordance with the New Jersey Pay Transparency Act and does not reflect the full value of our market-competitive total rewards package.
Associate Director Radiopharmaceutical Clinical Applications - Mid-Atlantic (NJ, PA, Washington DC, MD, DE) Lantheus Holdings IncAssociate Director Radiopharmaceutical Clinical Applications - Mid-Atlantic (NJ, PA, Washington DC, MD, DE)Somerset, NJRemote$163,000–$245,000 / yearIdentify, develop, and engage in long-term relationships with Key Opinion Leaders (KOLs) and Healthcare Providers (HCPs) in the assigned territory, including Nuclear Medicine Physicians, Radiologists, Radiation Oncologists, Technologists, Safety Officers, Health Physicists, Nursing Staff, and Advanced Practice HCPs at imaging facilities and medical centers. This role involves building and maintaining relationships with Key Opinion Leaders (KOLs) and Healthcare Providers (HCPs), providing advanced clinical and technical expertise, and ensuring the optimal use of our products in the clinical setting.
Sr. Specialist, Process Engineering - Oral Solid Dosage, Clinical Manufacturing (Onsite) Merck & Co IncSr. Specialist, Process Engineering - Oral Solid Dosage, Clinical Manufacturing (Onsite)Rahway, NJ$117,000–$184,200 / yearThe Non-Sterile Process Engineering team ensures right-first-time manufacture and delivery of high-quality drug products (spray-dried intermediates, tablets and capsules), leveraging pharmaceutical unit operations such as spray-drying, hot-melt extrusion, blending, roller compaction, encapsulation, compression, and film coating. Bachelor of Science degree in Chemical Engineering, Biomedical Engineering, Chemistry, Pharmaceutical Sciences or related scientific field with minimum of 5 years relevant experience, or a Master's degree with 3 years of relevant experience, or a PhD degree (with expected completion no later than June 2026).
Clinical Supply Support Specialist Services - FSP Parexel International CorpClinical Supply Support Specialist Services - FSPNJFrom clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Clinical Supply Monitoring & Activity Documentation (Electronic Trial Master File - eTMF).
Join our Talent Community for Clinical Specialists in IV Spine Ferring Pharmaceuticals, Inc.Join our Talent Community for Clinical Specialists in IV SpineParsippany, NJDemonstrated experience supporting the launch of a novel or disruptive therapy, including leading initial case support, training physicians on procedural techniques, and driving adoption through clinical workflow integration across office, ASC, and hospital settings. Active cross functional partners and coordinate with account leads to support the educational and technical needs within target accounts to ensure development of procedural expertise and confidence to deliver consistent, repeatable administration.
Clinical Intern Supervisor Seton Hall UniversityClinical Intern SupervisorSouth Orange, NJLogin Subscribe Keep informed about job opportunities at Seton Hall University Job Alert Human Resources Seton Hall Mission Statement Seton Hall: A Catholic University Human Resources Home Careers at Seton Hall. Special Instructions to Applicants: Applications should include the following documents: • Cover letter detailing applicable experience, interest, qualifications for the position, and commitment to diversity, equity, and inclusion • Curriculum vitae or resume • Two professional references with contact information including addresses, phone numbers, and email addresses.
Assistant Clinical Coordinator - Radiography Center Education GroupAssistant Clinical Coordinator - RadiographyBrooklyn, NY$90,000–$100,000 / yearMaintain an updated ABHES Faculty File Data Sheet including additional academic credentials earned and a record of Inservice and professional development completed annually in alignment with Faculty workload policies, faculty provide instruction for courses and complete administrative duties as assigned by the Program Director, Campus Director, or Director of Academic Affairs. Research and recommend appropriate agencies that would meet the identified educational requirements for clinical experiences for the students.
MFT Clinical Supervisor (80593) Iona UniversityMFT Clinical Supervisor (80593)bronxville, NYWith over 4,000 students, Iona offers small classes, engaged faculty, and a wide range of programs across the School of Arts & Science, the LaPenta School of Business (AACSB accredited), the NewYork Presbyterian Iona School of Nursing & Health Sciences, and the Hynes Institute for Entrepreneurship & Innovation. Recognized by The Princeton Review, The Wall Street Journal, Forbes, and U.S. News & World Report, Iona is nationally ranked for academic quality, social mobility, and long term return on investment.
Clinical Supervisor-CARE Somerset County, NJClinical Supervisor-CAREBridgewater, NJ$95,000–$105,000 / yearProvides clinical and administrative oversight of the daily operations and service implementation of the CARE program including group supervision, individual supervision, staff meetings, performance improvement, monthly reports, and curriculum oversight and crisis intervention. Provides clinical and administrative supervision in accordance with agency guidelines to those staff directly to assure effective and ethical delivery of trauma-informed, wellness and recovery, person-centered delivery of services.
Senior Project Manager - Oncology Precision Medicine Group LLCSenior Project Manager - OncologyNYRemote$147,300–$220,900 / yearThis compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. Ensure Quality management for assigned projects, including eTMF Inspection readiness, implementation of quality notification incident forms and / or corrective and preventative action plans to address any quality findings.