Senior Manager, Omnichannel Marketing Aurobindo Pharma LtdSenior Manager, Omnichannel MarketingEast Windsor, NJOFFICE POSITION - While performing the duties of this job the employee is required to: • Stand, sit; talk, hear, and use hands and fingers to operate a computer and telephone keyboard reach, stoop kneel to install computer equipment • Specific vision abilities required by this job include close vision requirements due to computer work • Light to moderate lifting is required • Moderate noise (i.e. business office with computers, phone, and printers, light traffic). • Ability to sit at a computer terminal for an extended period of time Sedentary work Exerting up to 10 pounds of force occasionally and/or negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects, including the human body.
Hospital Senior Account Manager, Anti-Infectives - Morristown, NJ / Allentown, PA/ Trenton, NJ GSK plcHospital Senior Account Manager, Anti-Infectives - Morristown, NJ / Allentown, PA/ Trenton, NJTrenton, NJRemote$165,000–$275,000 / yearCollaborate effectively across GSK's highly matrixed sales organization, partnering closely with Organized Provider Account Directors, Reimbursement Managers, and other cross-functional stakeholders to drive aligned execution and business success. This role engages Infectious Disease physicians, as well as hospitalists, pharmacists, case management teams, discharge planners, as well as key decision makers of IDNs (CMO, Pharmacy Directors, P&T Committee members) as needed, to drive sales.
Senior Manager Regulatory Affairs Advertising And Promotion SanofiSenior Manager Regulatory Affairs Advertising And PromotionMorristown, NJ$122,250–$176,583.33 / yearAs the Senior Manager, Regulatory Affairs Advertising and Promotion within our GRA Advertising and Promo Team, you will be responsible for conducting the independent review of advertising, promotional, communications and other materials, and help develop and implement regulatory strategies for promotion and advertising campaigns. With some direction from the Therapeutic Area Head, will conduct the independent review of advertising, promotional, communications and other materials, and help develop and implement regulatory strategies for promotion and advertising campaigns, including serving as regulatory lead for product launches.
Sr. Director, Epidemiology, Immunology - Hampton, NJ Celldex TherapeuticsSr. Director, Epidemiology, Immunology - Hampton, NJHampton, New Jersey$203,157–$263,841 / yearLead the design and execution of post-marketing requirement studies, retrospective database analyses, literature reviews, chart reviews, registries, and external comparator or natural history studies, and support observational studies and other prioritized data generation initiatives. The Director will work closely with Clinical Development, Biostatistics, Pharmacovigilance, Regulatory Affairs, Medical Affairs, HEOR, Commercial, and external partners to design and deliver high-quality epidemiologic research in a fast-moving, entrepreneurial environment.
Senior Medical Science Liaison _ New York Celldex TherapeuticsSenior Medical Science Liaison _ New YorkHampton, New Jersey$133,579–$213,380 / yearMSL) will prioritize contacts with key opinion leaders (KOLs), healthcare providers, and clinical investigators within an assigned U.S. region, providing scientific exchange and supporting the generation of actionable insights. MSL is expected to deliver scientifically accurate, relevant, and increasingly insightful discussions, gather and communicate insights from the field, and support execution of regional priorities.
Senior Medical Science Liaison _ South Central Celldex TherapeuticsSenior Medical Science Liaison _ South CentralHampton, New Jersey$133,579–$213,380 / yearMSL) will prioritize contacts with key opinion leaders (KOLs), healthcare providers, and clinical investigators within an assigned U.S. region, providing scientific exchange and supporting the generation of actionable insights. MSL is expected to deliver scientifically accurate, relevant, and increasingly insightful discussions, gather and communicate insights from the field, and support execution of regional priorities.
Senior Medical Science Liaison _ North Central Celldex TherapeuticsSenior Medical Science Liaison _ North CentralHampton, New Jersey$133,579–$213,380 / yearMSL) will prioritize contacts with key opinion leaders (KOLs), healthcare providers, and clinical investigators within an assigned U.S. region, providing scientific exchange and supporting the generation of actionable insights. MSL is expected to deliver scientifically accurate, relevant, and increasingly insightful discussions, gather and communicate insights from the field, and support execution of regional priorities.
Senior Medical Science Liaison _ Southeast Celldex TherapeuticsSenior Medical Science Liaison _ SoutheastHampton, New Jersey$133,579–$213,380 / yearMSL) will prioritize contacts with key opinion leaders (KOLs), healthcare providers, and clinical investigators within an assigned U.S. region, providing scientific exchange and supporting the generation of actionable insights. MSL is expected to deliver scientifically accurate, relevant, and increasingly insightful discussions, gather and communicate insights from the field, and support execution of regional priorities.
Senior Medical Science Liaison _ Mountain West Celldex TherapeuticsSenior Medical Science Liaison _ Mountain WestHampton, New Jersey$133,579–$213,380 / yearMSL) will prioritize contacts with key opinion leaders (KOLs), healthcare providers, and clinical investigators within an assigned U.S. region, providing scientific exchange and supporting the generation of actionable insights. MSL is expected to deliver scientifically accurate, relevant, and increasingly insightful discussions, gather and communicate insights from the field, and support execution of regional priorities.
NewWW Senior Inventory Manager WCH (BR) 6029-MEDICAL DEVICE BUSINESS SERVICES Legal EntityWW Senior Inventory Manager WCH (BR)Raritan, New JerseyCompetitive Landscape Analysis, Consulting, Cost Management, Data Savvy, Demand Planning, Distribution Resource Planning (DRP), Financial Competence, Inventory Management, Inventory Optimization, Inventory Turnover, Logistics Optimization, Manufacturing Flow Management, Mentorship, Organizing, Strategic Supply Chain Management, Supply Planning, Technical Credibility This position will work very closely with the Regional Planning, Supply Network Planning, and Product Planning and Logistics organizations to ensure that inventory levels are optimized, and the supply chain is delivering all commitments in this area.
Senior Clinical Research Director SanofiSenior Clinical Research DirectorMorristown, NJ$236,250–$393,750 / yearProvide appropriate medical input and support for all activities related to clinical studies, including medical training, feasibility assessments, medical review of data, and medical information for study teams, medical advisors, Clinical Project Leaders from Clinical Study Units, and investigators. We are looking for a Senior Clinical Research & Development (CRD) to join our Rheumatology/Transplant clinical development team, playing a pivotal leadership role in shaping and advancing our clinical programs.
Senior Scientist, Regulatory & Clinical Operations hims & hersSenior Scientist, Regulatory & Clinical OperationsSouth Plainfield, NJYou Have: PhD in Clinical Chemistry, Biochemistry, Analytical Chemistry, Molecular Biology, or related field with 4+ years; OR Master's degree with 7+ years; OR Bachelor's degree with 10+ years of relevant bench experience in a diagnostic or clinical laboratory setting. The ideal candidate is comfortable operating at the intersection of bench science and clinical study execution, translates regulatory rigor into practical day-to-day decisions, and thrives working independently in a fast-moving environment.
Senior Regulatory Affairs Specialist - Software OrganOxSenior Regulatory Affairs Specialist - SoftwareMadison, NJ$115,000–$140,000 / yearUnder direction from the Director, Regulatory Affairs, Software and Innovation, the Senior Regulatory Affairs Specialist will be responsible for: · Providing regulatory affairs support for projects related to Digital Health, Software, Cybersecurity, Electromechanical devices and Regulatory Intelligence. Founded in 1921, Terumo Corporation strives to fulfill its mission of “Contributing to Society through Healthcare” by providing a comprehensive range of solutions in the fields of therapeutic procedures, hospital operations, and life sciences in more than 160 countries and regions.
Epic Optime Senior Consultant DeloitteEpic Optime Senior ConsultantMorristown, NJ$91,100–$179,500 / yearThe wage range for this role 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. Our purpose comes through in our work with clients that enables impact and value in their organizations, as well as through our own investments, commitments, and actions across areas that help drive positive outcomes for our communities.
Senior Manager Regulatory Affairs Advertising and Promotion SanofiSenior Manager Regulatory Affairs Advertising and PromotionMorristown, NJ$122,250–$176,583.33 / yearAs the Senior Manager, Regulatory Affairs Advertising and Promotion within our GRA Advertising and Promo Team, you will be responsible for conducting the independent review of advertising, promotional, communications and other materials, and help develop and implement regulatory strategies for promotion and advertising campaigns. With some direction from the Therapeutic Area Head, will conduct the independent review of advertising, promotional, communications and other materials, and help develop and implement regulatory strategies for promotion and advertising campaigns, including serving as regulatory lead for product launches.
Senior Professional Contract Administrator SanofiSenior Professional Contract AdministratorMorristown, NJ$85,500–$123,500 / yearThe Senior Professional Contract Administrator will be primarily responsible for interacting with Account Management representatives, internal functional teams, wholesaler and distributors and external customers to provide contract information. Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave.
NewSenior Manager, Clinical Data Management PTC Therapeutics IncSenior Manager, Clinical Data ManagementWarren, NJ$129,500–$163,100 / yearResponsible for data management activities, database cleaning and lock activities including developing data management plans, supervising database development, and reviewing and processing clinical trial data to ensure completeness, accuracy, and consistency of clinical trials databases. Participate in cross functional team meetings as requested and communicate with all departments regarding project statuses/issues, provide ongoing feedback on data management workflows to increase efficiency and provide feedback to CRAs.
Admissions Registered Nurse Bayada Home Health Care, Inc.Admissions Registered NurseSomerset, NJ$65–$75 / hourThis is a great opportunity for an experienced home health nurse who enjoys clinical assessment, autonomy, care coordination, and building strong relationships with clients and families from the very first visit. How You'll Make an Impact: Complete comprehensive OASIS Start of Care (SOC) admissions visits for home health clients throughout the assigned territory.
Senior Director, Regulatory Affairs Merck & Co IncSenior Director, Regulatory AffairsNorth Wales, PA$173,200–$272,600 / yearRequired Skills: Business Alignment, Cross-Functional Project Management, Decision Making, Global Regulatory Submissions, Goal Setting, Interpersonal Relationships, Negotiation, People Leadership, Policy Reviews, Policy Revisions, Regulatory Affairs Management, Regulatory Communications, Regulatory Compliance, Regulatory Documents, Regulatory Experience, Regulatory Management, Regulatory Processes, Regulatory Reporting, Regulatory Strategies, Regulatory Submissions, Stakeholder Negotiations, Strategic Planning, Strategic Thinking. Summary of Responsibilities: Leads a team of promotional regulatory reviewers (senior specialists, associate directors, and individual contributor directors) to provide regulatory strategy across multiple therapeutic franchises for pipeline and in-line products that competitively positions our company's products, consistent with applicable FDA regulations and company policies for US advertising and promotion.
Senior Clinical Research Associate Terumo Medical CorpSenior Clinical Research AssociateSomerset, NJ$92,320–$126,940 / yearSupport the investigator evaluation and recruitment process: o Create phone scripts, questionnaires, and other assessment tools for use in the selection of sites; o Assist team in the development of site recruitment and retention strategy; o Initiate contact with PIs, conduct pre-visits, assess potential investigators and recommend suitability of the site; Assist clinical team with study start-up activities: o Assist in development of protocol / ICF / CRF / CRF completion guidelines, preparation and maintenance of monitoring plans, study binders, study manuals, and other site specific and monitoring tools; o Requests and collects initial regulatory documentation; o Ensure that sites fulfill their regulatory obligations and submit study documents for IRB review and approval; o Performs study tracking and advises PM when an investigational site is approved and ready to receive investigational device supplies; Site Management and study execution activities: o Plan and conduct training / site initiation, interim and close-out visits. Thorough understanding of operational aspects of clinical research and regulatory regulations; Good interpersonal, problem solving and communication skills; Excellent follow-through capability; Self-motivated, attention to detail and organizational skill; Experience with various computer systems / applications and clinical trial management systems; willingness to learn new systems / databases as needed.