Clinical Care Technician Intensive Care Unit - Full Time Night RWJ Barnabas Health Medical IncClinical Care Technician Intensive Care Unit - Full Time NightHamilton, NJ$21.29–$26.71 / hourRWJBarnabas Health is the premier health care destination providing patient-centered, high-quality academic medicine in a compassionate and equitable manner, while delivering a best-in-class work experience to every member of the team. Some of the responsibilities include but are not limited to: Taking vital signs, EKGS, performing phlebotomy, assisting or providing patients with bedside care, i.e. bathing, mouth care, skin care.
FSP Senior Research Scientist-Dissolution Method Development Thermo Fisher ScientificFSP Senior Research Scientist-Dissolution Method DevelopmentCollegeville, PennsylvaniaWithin our Analytical Services team, we have a functional service provider solution, which is an outstanding partnership that allows our customers to use the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.
Imaging Clinical Research Physician Eli Lilly and CoImaging Clinical Research PhysicianPhiladelphia, PA$198,000–$389,400 / yearOur current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women's Initiative for Leading at Lilly (WILL). Serve as a scientific expert in molecular imaging modalities, including PET, SPECT, CT, and MRI (e.g., imaging of vascular and myocardial inflammation, autoimmune disease activity, atherosclerotic plaque, and cardiac amyloidosis), with applicability to oncology and emerging theranostic platforms a plus.
Scientist: Steriles Packaging Development Thermo Fisher Scientific IncScientist: Steriles Packaging DevelopmentCollegeville, PAWith clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Tasks: Perform timely execution of lab based analysis, including experiment write up to support sterile primary package selection, integrity, stability, and lifecycle for the coordination and testing of samples.
Senior Manager, Contracts ICON PlcSenior Manager, ContractsPhiladelphia, PADocumentation ownership and repository management: Ensure timely maintenance and distribution of contracting documentation, including a complete, version controlled repository of signed CSAs, amendments, rate cards, and budget approvals across the portfolio; ensure eTMF completeness and inspection readiness.-controlled repository of signed CSAs, amendments, rate cards, and budget approvals across the portfolio; ensure eTMF completeness and inspection readiness. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development What You Will Do: Contracts and budget strategy and oversight: Set up and lead the end-to-end operational strategy for study contracting and budgeting across assigned studies and programs, aligning with CSP, country requirements, biosampling plans, and funding envelopes.
Clinical Specialty Representative - Eastern Pennsylvania Mayo ClinicClinical Specialty Representative - Eastern PennsylvaniaPA$155,600–$192,416 / yearIn collaboration with Product Managers and the CSR Director, Regional Director of Sales, Regional Managers identify specific tests or groups of tests that are differentiated in the market and pursue upsells to targeted clients. Today, our employees are located at our three major campuses in Phoenix/Scottsdale, Arizona, Jacksonville, Florida, Rochester, Minnesota, and at Mayo Clinic Health System campuses throughout Midwestern communities, and at our international locations.
Clinical Fellow (CF) Speech Language Pathologist (SLP) Kaleidoscope Education SolutionsClinical Fellow (CF) Speech Language Pathologist (SLP)Philadelphia, Pennsylvania$2,520Serves as a member of the school’s multidisciplinary team, IEP program team, and offers consultation and collaboration with school staff and parents in support of student goals. Develop treatment plans, in conjunction with instructional staff, that are strength-based, as well as child and family-centered for overall educational improvement.
Associate Research Scientist, Bioassay Thermo Fisher Scientific IncAssociate Research Scientist, BioassayCollegeville, PAThe role reliably conducts complex sample preparation and analysis following validated and experimental procedures with limited supervision, maintains data integrity in accordance with SOPs, protocols, and product specifications, and works collaboratively with project teams to support method execution, troubleshooting, and continuous improvement of bioassay workflows. Role Summary: Perform biological assays and GMP sample testing to support drug development and commercial projects, with a primary focus on routine GMP sample testing support, cell banking activities, and execution of all associated project and sample-testing tasks.
Clinical Retention Specialist (North-MA, NY, PA, NJ, ME, CT, RI, NH, VT ) Insulet CorpClinical Retention Specialist (North-MA, NY, PA, NJ, ME, CT, RI, NH, VT )Philadelphia, PARemote$79,300–$118,900 / yearInsulet's flagship innovation, the Omnipod 5 Automated Insulin Delivery System, integrates with a continuous glucose monitor to manage blood sugar with no multiple daily injections, zero fingersticks, and can be controlled by a compatible personal smartphone in the U.S. or by the Omnipod 5 Controller. Identify early indicators of disengagement or churn through data assessment and analytics in partnership with the data science teams and collaborate with Customer Success teams to deploy targeted, regionally informed save strategies.
Health Care Case Manager (Registered Nurse) Camden South-Cherry Hill, NJ Rutgers The State University of New JerseyHealth Care Case Manager (Registered Nurse) Camden South-Cherry Hill, NJNJDo you have a minimum of 1-2 years of full-time clinical experience as a pediatric nurse in pediatric environments such as Pediatric doctor's offices, Pediatric Hospital unit, Pediatric public health nursing, Pediatric Emergency department/Pediatric Critical Care unit, Family Practice offices, school nurse, child welfare nursing, Pediatric/Juvenile Mental/Behavioral health facilities, or Children's hospital?. Minimum of 1-2 years of full-time clinical experience as a pediatric nurse in pediatric environments such as Pediatric doctor's offices, Pediatric Hospital unit, Pediatric public health nursing, Pediatric Emergency department/Pediatric Critical Care unit, Family Practice offices, school nurse, child welfare nursing, Pediatric/Juvenile Mental/Behavioral health facilities, or Children's hospital.
NewQuality Risk Management Manager Pride GlobalQuality Risk Management ManagerPrinceton, NJ$50–$60 / hourResponsibilities: Partner closely with Clinical Operations, Data Management, Pharmacovigilance, Regulatory Affairs, CROs, and other R&D stakeholders to identify compliance risks, develop performance metrics, conduct root cause analysis, and drive continuous process improvement. This applies to direct care staff (Examples: RN, LPN, Nurse Aides, Therapists) referred to Kentucky nursing facilities, assisted living communities, or long-term care facilities, in accordance with KRS 216.793.
Integrated Study Timeline Manager ICON PlcIntegrated Study Timeline ManagerBlue Bell, PA5+ years' experience in pharmaceutical industry and/or clinical research organization, including 3+ years clinical study management/oversight, including significant study management support experience (e.g., clinical trial assistant/associate or lead CRA). Working as an Integrated Study Timeline Implementation Manager exclusively assigned to a Pharmaceutical Company, you will lead development, customization, and maintenance of the Integrated Study Timelines (IST) for clinical trials using global timeline templates.
Supply Chain Quality Manager - Operations Signant Health Management LtdSupply Chain Quality Manager - Operationshorsham, PAServe as the internal SME on transportation regulations for clinical devices containing lithium batteries and for medical devices - covering IATA DGR, IMDG, 49 CFR (DOT/PHMSA), and UN 38.3 test requirements; review and approve shipping configurations, packaging specifications, and dangerous goods documentation across the global warehouse network. Maintain Signant Healths supply chain QMS in alignment with ISO 13485:2016 (incorporated into FDA QMSR / 21 CFR Part 820), EU MDR, and UK HSE requirements; monitor evolving regulations across consumer electronics (FCC, CE, WEEE/e-waste) and medical devices and proactively update internal policies, SOPs, and quality agreements.
Senior Director, Clinical Development Mallinckrodt LLCSenior Director, Clinical DevelopmentBridgewater, NJ$285,000–$315,000 / yearEnsure CD contributions to trial-related documents such as the IBs, ICF, CRFs, CRF Completion Guidelines, Study Execution and Monitoring Plans, Clinical Data Review Plan, Clinical Database specifications, statistical analysis plan, the data management plan, the safety management plan, the medical monitoring plan, Clinical Study Report (CSR) etc. Work collaboratively with the clinical study team and other team members to prepare abstracts, manuscripts and presentations for external meetings as well as author clinical sections of regulatory documents (CSRs, IBs, IND sections, CTAs, ISS and ISE sections and clinical expert reports).
Global Study Manager ICON PlcGlobal Study ManagerBlue Bell, PAAccountable for ensuring country-level feasibility is completed in collaboration with cross functional GSSO colleagues and Operational Analytics & Quantitative Sciences (OAQS) organization and pCRO (as applicable) reviewing Pre-trial Assessment outputs, approving sites, and assessing site activation plans. Development, review or approval of the Study Startup, Study Monitoring & protocol recruitment plans and others (e.g., CRF Guidelines, IMPALA manual, Training Plan, etc.) The Global Study Manager can delegate development of plans or components of plans to Study Operational Managers (if assigned) or CSTAs as appropriate.
Senior Project Manager, Laboratory ICON PlcSenior Project Manager, LaboratoryBlue Bell, PAAct as the sponsors main contact person in all matters regarding our central laboratory services, following up and responding to clinical study specific inquiries from Sponsors, Physicians, CRA and CRO representatives and the ICON Site Services Department. Key responsibilities include: Ensure client satisfaction by acting as the Client's main contact in all matters regarding ICON Central Laboratories' (ICL) services, including the setup and day-to-day management of studies.
Senior Study Manager - Infectious Disease/Vaccines (Pragmatic trials) - US/Canada ICON PlcSenior Study Manager - Infectious Disease/Vaccines (Pragmatic trials) - US/CanadaBlue Bell, PAManages all HQ Operational Activities, including: Establishes, leads and manages Clinical Trial Team (CTT) Supports clinical (drug/vaccine) supplies planning. Excellent oral (including presentation) and written communication, computer/database management, and project management skills required.
Manager, Medical Writing ICON PlcManager, Medical WritingBlue Bell, PACollaborating closely with cross-functional teams including clinical, regulatory, and project management teams to ensure alignment and accuracy in documentation. As a Manager, Medical Writing at ICON, you will lead a team of medical writers to produce high-quality, scientifically accurate documents in support of clinical trials.
Mgr, Database Management Systems IQVIA Holdings IncMgr, Database Management SystemsPhiladelphia, PA$84,600–$211,600 / yearDeveloping strong and productive working relationships with key stakeholders throughout CDMs, Clinical Ops, and Kite with the ability to think strategically across a broad portfolio and effectively express their views to senior management. Strong knowledge of industry-leading EDC tools (e.g., Medidata Rave, Veeva, Medrio, Oracle, TrialGrid, etc.) and well-versed in industry trends and emerging technologies supporting data collection.
Senior Clinical Informaticist - Clinical informatics Team Thomas Jefferson UniversitySenior Clinical Informaticist - Clinical informatics TeamPhiladelphia, PennsylvaniaJefferson is more than 65,000 people strong, dedicated to providing the highest-quality, compassionate clinical care for patients; making our communities healthier and stronger; preparing tomorrow's professional leaders for 21st-century careers; and creating new knowledge through basic/programmatic, clinical and applied research. 5501 Old York Road, Philadelphia, Pennsylvania, United States of America Nationally ranked, Jefferson, which is principally located in the greater Philadelphia region, Lehigh Valley and Northeastern Pennsylvania and southern New Jersey, is reimagining health care and higher education to create unparalleled value.