Product Development Research Scientist II Tris Pharma IncProduct Development Research Scientist IIMonmouth Junction, NJ$90,000–$115,000 / yearThe PD Research Scientist II plans and executes pre-formulation and formulation activities, contributing to development of novel drug delivery platforms and differentiated products from conceptualization to pilot proof of concept (PoC) thereby creating commercially viable intellectual property (IP). Tris Pharma, Inc. (www.trispharma.com) is a leading privately-owned US biopharmaceutical company focused on development and commercialization of innovative medicines in ADHD, spectrum disorders, anxiety, pain and addiction addressing unmet patient needs.
Oncology Research Regulatory Coordinator II PRN Cooper University Health CareOncology Research Regulatory Coordinator II PRNCamden, NJThe role of Oncology Research Regulatory Coordinator will serve as the regulatory lead on industry-sponsored, federally funded or MD Anderson collaborative studies maintaining compliance and audit readiness. Our extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols.
Research Fellow- Multimodal Perception, VLA Models, and Autonomous Roboti Varian Medical Systems IncResearch Fellow- Multimodal Perception, VLA Models, and Autonomous RobotiPCT$43–$56 / hourIt 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.". How we work: When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual's potential to contribute with diverse ideas.
Oncology Research Coord II PRN Cooper University HospitalOncology Research Coord II PRNCamden, New JerseyPer diemThe role of the Oncology Research Coordinator I provides the oversight of clinical studies in the oncology setting managing Quality of Life and specimen trials, while continuing to learn and advance in experience to manage oncology treatment trials. Work with sponsors to set up site initiation visits, monitoring visits and study close-out visits and prepare post-visit documents.
NewOncology Research Coordinator Penn MedicineOncology Research CoordinatorPlainsboro, NJ$55,607.14–$88,682.88 / yearImplement, refine, and carry out protocols for multiple research studies, while maintaining the quality of intervention processes, maximizing recruitment and retention of study participants, minimizing missing data, and performing data quality control checks. Participate in the development/maintenance of IRB submissions and regulatory files, including submission of study documents to all applicable institutional committees (e.g., IRB, CTSRMC) for initial approval, continuing reviews, adverse events, and approval of any amendments.
Research Specialist Princeton UniversityResearch SpecialistPrinceton, New Jersey$41,000–$60,000 / yearFull timeOverview: Princeton University's Neuroscience Institute seeks applicants for a Research Assistant position in a premiere research laboratory whose work focuses on neural circuits for social communication and sensorimotor integration using the fruit fly Drosophila as a model system (see murthylab.princeton.edu ). Research in the lab employs state-of-the-art neuroscience approaches, including quantitative behavior analyses, computational modeling, neural recordings, connectomics, molecular biology, and genetic tools.
Associate Director, Outcomes Research Merck & Co IncAssociate Director, Outcomes ResearchNorth Wales, PA$156,900–$247,000 / yearUnder the guidance of a senior leader, an Associate Principal Scientist/Associate Director, has primary responsibility for planning/managing real world and economic evidence activities for in-line and pipeline products to meet the value evidence needs of clinicians, payers, policymakers, HTA/reimbursement agencies, and health systems globally. Types of studies executed include prospective and retrospective observational studies to characterize disease burden and epidemiology, treatment patterns, healthcare resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses, and economic modelling.
Senior Director, Global Real-World Evidence & Health Outcomes Research Lead, Specialty Medicines GSK plcSenior Director, Global Real-World Evidence & Health Outcomes Research Lead, Specialty MedicinesPhiladelphia, PAThe role of Senior Director, Global Real-World Evidence & Health Outcomes Research (GRWE& HO) Lead is critical to achieving this ambition by ensuring that each medicine GSK brings to market is supported by scientifically credible, high-quality evidence that drives competitiveness and strong evidence-based product positioning, value propositions and value-based pricing. The Senior Director, Global Real-World Evidence & Health Outcomes Research Lead will be accountable for ensuring team members engage closely with medical and matrix stakeholders and partner effectively in data generation plan (DGP) planning, design, execution, translation, and dissemination for the specialty asset.
Director, Qualitative Market Research DesignDirector, Qualitative Market ResearchDoylestown, PennsylvaniaDemonstration of a deep understanding of the market research needs of pharmaceutical and biotech products in various stages of the product life cycle (Phase 2 through Phase 4 clinical trials, pre-launch promotional development, in-line/mature products). If you’re looking for a company that strives to create a work environment that encourages and compliments you, you’re curious, a critical thinker able to think outside the box, like challenges and are passionate about what you do, we definitely want to speak with you!
Oncology Research Regulatory Coordinator II PRN Cooper University HospitalOncology Research Regulatory Coordinator II PRNCamden, New JerseyPer diemThe role of Oncology Research Regulatory Coordinator will serve as the regulatory lead on industry-sponsored, federally funded or MD Anderson collaborative studies maintaining compliance and audit readiness. Our extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols.
Research Administrator - CNI Cooper University HospitalResearch Administrator - CNICamden, NJAll processes related to grant proposals and research funding at the institute level with an emphasis on post-award financial monitoring, tracking, and reporting to Institute leadership and faculty researchers. The position works closely with Institute leadership, faculty researchers, and ORSP teams, and Finance while leveraging knowledge of grant and contract management regulations, institutional policies and financial analyses.
NewResearch Scientist-PRN Cooper University HospitalResearch Scientist-PRNCamden, New JerseyPer diemAccountable to the Primary Investigator and Director of Grants and Research, this role conducts specific research projects related to Addiction Medicine Services in inpatient, outpatient, and community-service environments. The Research Scientist will provide intellectual and technical support to research programs and initiatives, including utilization of implementation of science approaches and best practice.
2027 Future Talent Program - Research Initiation & Budget Execution - Intern Merck & Co Inc2027 Future Talent Program - Research Initiation & Budget Execution - InternNorth Wales, PA$39,908–$111,111 / yearAI & Digital Tool Enablement: Partner with team members to pilot, test, evaluate, or enhance innovative AI-enhanced tools and specialized platforms (e.g., the Non-Interventional Research (NIR) Vendor Grading Tool) aimed at automating manual tasks, tracking deliverables, or streamlining literature reviews. The internship lasts up to 12 weeks and will focus on multiple projects centered around process improvement, workflow optimization, and the integration or evaluation of AI-enhanced tools (such as specialized non-interventional research platforms, automated budget management applications, or literature-screening AI tools).
Research Pharmacy Technician--HUP--Investigational Drug Pharmacy Penn MedicineResearch Pharmacy Technician--HUP--Investigational Drug PharmacyPhiladelphia, PAUnder the supervision of the IDS pharmacist, the role is responsible for providing patient care services to patients enrolled in clinical trials, oversee investigational drug inventory and storage, including record keeping and drug accountability, ordering and receiving products, tracking expiration dates, processing drug returns and destruction after study closure. Ensures proper distribution/delivery of investigational pharmaceutical and supply shipment, provide support for drug procurement staff including unpacking stock, documenting receipt, and proper storage.
Research Project Interviewer - On site - Philadelphia Schlesinger GroupResearch Project Interviewer - On site - PhiladelphiaPhiladelphia, PAThe Research Project Interviewer (RPI) plays a critical role in the successful execution of research studies by supporting subject recruitment, informed consent, study visits, investigational product handling, and study documentation. Collaborate effectively with monitors, the Clinical Project Management team, and site staff to support overall study success.
Research Project Interviewer - NJ - On site Schlesinger GroupResearch Project Interviewer - NJ - On siteIselin, NJThe Research Project Interviewer (RPI) plays a critical role in the successful execution of research studies by supporting subject recruitment, informed consent, study visits, investigational product handling, and study documentation. Collaborate effectively with monitors, the Clinical Project Management team, and site staff to support overall study success.
Foundation AI Research Scientist Siemens HealthineersFoundation AI Research ScientistPrinceton, NJFull timeIt 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 research, design, and develop large-scale AI models capable of learning and reasoning across complex medical data, including medical imaging, clinical text, electronic health records, real-time monitoring data, and other healthcare information.
Associate Principal Scientist, Preclinical Research Cabaletta Bio IncAssociate Principal Scientist, Preclinical ResearchPhiladelphia, PAThe successful candidate will work in discovery research as a molecular biology and gene delivery subject matter expert, collaborating cross-functionally with other teams within discovery research (Cellular Immunology, Pharmacology, CMC, etc) and more broadly with other departments in Cabaletta to establish a product pipeline and to support preclinical IND enabling studies. Responsibilities: Management of a team of employees that are responsible for executing R&D experiments, designing and implementing assays, and supporting reagent production to enable short and long-term success.
NewIn-House Clinical Research Associate Novo Nordisk ASIn-House Clinical Research AssociatePlainsboro, NJ$100,000–$120,000 / yearSite Support: Serve as the primary point of contact for clinical trial sites, offering guidance, support, and training as needed to ensure trial targets are met as well as protocol and regulatory compliance; triaging support requests to appropriate trial team members as appropriate; work closely with CRAs in overall site management. Builds and maintains strong relationships with external stakeholders relevant to the execution of clinical trials and support of clinical trial sites (e.g., clinical trial site staff, IRBs, clinical research vendors).
Postdoctoral Research Fellow - Fathi Kazerooni Children's Hospital of PhiladelphiaPostdoctoral Research Fellow - Fathi KazerooniPhiladelphia, PAWe are seeking a highly motivated Postdoctoral Research Fellow to join a multidisciplinary research team focused on developing and translating artificial intelligence (AI) methods for pediatric neuro-oncology. If you are applying for a Research Post-Doctoral Fellow role, please refer to this link for salary guidelines (copy & paste into your browser): https://www.research.chop.edu/services/hiring-a-postdoctoral-fellow#collapse-accordion-3523-3 .