Director, WW Medical I&CV, Professional Societies Immunology Bristol-Myers Squibb CoDirector, WW Medical I&CV, Professional Societies ImmunologyPrinceton, NJ$207,490–$251,433 / yearWork extensively with BMS senior leaders across multiple departments at BMS including Immunology Development, Discovery, Translational Medicine, HQ and Worldwide Medical, Commercial, Public Affairs, Access and Clinical Operations (as needed) to optimize BMS interactions with the professional societies and professional associations. This role works closely with the Portfolio Strategy Head and the Medical teams and additional key internal stakeholders to create and initiate innovative strategies for engagement with professional societies, including initiatives and programs in alignment with specific therapeutic area strategic imperatives.
Director, Statistical Programming Definium Therapeutics IncDirector, Statistical ProgrammingNY$216,951–$241,497 / yearOur lead product candidate, lysergide tartrate (our proprietary orally disintegrating tablet form of lysergide (LSD) D-tartrate), represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Proficient in statistical computational software such as SAS, including complicated data steps, SAS macro languages, and commonly used analysis procedures (e.g., PROC Freq, PROC REPORT, PROC GLM, and PROC MIXED).
Director, Regulatory Strategist, GRS Bristol-Myers Squibb CoDirector, Regulatory Strategist, GRSPrinceton Pike, NJ$240,940–$291,964 / yearProvide strategic regulatory input to key development documents and study reports, including Clinical protocols, clinical reports/summary documents, nonclinical reports/summary documents Nonclinical and clinical summary documents, Analysis Plans and DMC Charters. Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
Medical Director, GMA - Bladder Cancer Johnson & JohnsonMedical Director, GMA - Bladder CancerRaritan, NJ$160,000–$270,000 / yearRequired Skills: Preferred Skills: Analytical Reasoning, Business Requirements Analysis, Clinical Research and Regulations, Clinical Trials Operations, Communication, Developing Others, Digital Culture, Digital Literacy, Healthcare Trends, Inclusive Leadership, Leadership, Medical Affairs, Medical Communications, Medical Compliance, Product Strategies, Stakeholder Analysis, Strategic Thinking, Workflow Analysis. This role is responsible and accountable for providing evidence-based, clinical and scientific expertise to internal and external partners, support cross-functional teams to identify medical barriers and opportunities across the bladder cancer portfolio and implement medical affairs tactics and initiatives.
Director, Pediatric Intensive Care Unit (PICU) – Cooperman Barnabas Medical Center RWJBarnabas Health RWJBarnabas HealthDirector, Pediatric Intensive Care Unit (PICU) – Cooperman Barnabas Medical Center RWJBarnabas HealthLivingston, NJ$225,000–$375,000 / yearCBMC is located in Northern New Jersey in Essex County, which is an ideal location to reside with easy access to the Jersey Shore, NYC, beautiful suburban neighborhoods, diverse communities, and top-notch school districts -- plus access to museums, fine dining and great shopping! The close Rutgers affiliation makes available research resources outside of CBMC including a Clinical Research Center, Clinical Trials Office, and other extensive resources present at Rutgers as the State University of New Jersey.
Director, Global Medical Evidence Generation Lead, Hematology Bristol-Myers Squibb CoDirector, Global Medical Evidence Generation Lead, HematologyPrinceton, NJ$207,490–$251,433 / yearThe Medical Evidence Generation (MEG) Lead, in Medical Affairs, will lead the strategic development and execution of a robust evidence generation plan within the hematology portfolio, including Clinical Research Collaborations (CRCs), Medical Affairs Sponsored Trials (MAST), and Investigator-Sponsored Research Studies (ISRs), designed to: Uncover new clinical development opportunities that will maximize the benefit our medicines can bring to patients. Responsibilities will include, but are not limited to, the following: Define and drive the integrated evidence generation strategy aligned with Medical Affairs and overall product strategy, spanning clinical trials (Phase II/IV), real-world evidence (RWE), non-interventional studies, registries, observational research, and health outcomes studies.
Director of Finance - Sunset Park, Brooklyn NYU Langone HealthDirector of Finance - Sunset Park, BrooklynBrooklyn, NY$200,000–$220,000Full timeThe Director of Clinical Finance & Finance Site Leader oversees the portfolios clinical finance staff and works with various departments and leadership to operationalize the financial goals and objective of the organization. The Director of Clinical Finance & Finance Site Leader is a member of the NYU Langone Health Finance leadership team and assumes responsibility for the clinical finance functions of the designated portfolio(s).
NewDirector, HTA, Value & Evidence (HV&E) - I&I Pipeline, Specialty Care PfizerDirector, HTA, Value & Evidence (HV&E) - I&I Pipeline, Specialty CareNew York City, New YorkLead the timely development of launch deliverables including value & evidence strategy, global value dossiers/AMCP/JCA dossiers, systematic literature reviews, economic models, and innovative tools to successfully support reimbursement and access requirements in partnership with the regions/countries. Develop patient-reported outcomes strategy and incorporate humanistic and economic endpoints into clinical trials across all phases of product development to build comprehensive trial-based evidence aligned with overall asset strategy and to ensure global reimbursement and access requirements.
Medical Director, Medical Affairs, ALS Shionogi Inc.Medical Director, Medical Affairs, ALSFlorham Park, New Jersey$230,000–$280,000 / yearDevelop and maintain excellent working relationships with both US and global Clinical Development, Marketing, and Regulatory functions, ensuring seamless communications and provision of up to date scientifically accurate clinical information to external and internal sources. Overview: The Medical Director will be responsible for developing and overseeing the execution of Medical Affairs programs in the US that support pre-approval, marketed, and late development products and compounds with a focus on ALS, rare disease.
Senior Director, Data Sciences and Advanced Analytics Bristol Myers SquibbSenior Director, Data Sciences and Advanced AnalyticsPrinceton, NJ$259,990–$315,046 / yearAs a key leader of the Data Science and Advance Analytics (DSAA) organization in drug development is part of a cross-functional team of drug development scientists and data scientists focused on providing hands on skills, expertise, and tools to facilitate access, integration, visualization, and exploratory analysis of complex and diverse data in support of clinical development activities and decisions. The Data Science Lead will collaborate with Biostatistics leads and other members of drug development teams to ensure connectivity of exploratory analysis work in support of development, regulatory approval, and market acceptance of Bristol-Myers Squibb (BMS) products.
Director, WW Medical I&Cv, Professional Societies Immunology Bristol Myers SquibbDirector, WW Medical I&Cv, Professional Societies ImmunologyPrinceton, NJ$207,490–$251,433 / yearWork extensively with BMS senior leaders across multiple departments at BMS including Immunology Development, Discovery, Translational Medicine, HQ and Worldwide Medical, Commercial, Public Affairs, Access and Clinical Operations (as needed) to optimize BMS interactions with the professional societies and professional associations. This role works closely with the Portfolio Strategy Head and the Medical teams and additional key internal stakeholders to create and initiate innovative strategies for engagement with professional societies, including initiatives and programs in alignment with specific therapeutic area strategic imperatives.
Associate Director, Global Medical Cardiovascular, Mavacamten Bristol Myers SquibbAssociate Director, Global Medical Cardiovascular, MavacamtenPrinceton, NJ$166,350–$201,571 / yearThe Associate Director operates in a highly collaborative environment with a team that manages a diversified matrix and partners closely with US Medical, Regional Market Medical, Medical Communications, Clinical Development, Regulatory, Safety, Market Access, Marketing, and Commercial teams. This role provides scientific and clinical leadership across global deliverables-including core content and scientific materials, congress planning support, medical education, and cross-functional scientific engagement-to ensure timely, high-quality support for US priorities and milestones.
Director, Data, Data Science And Artificial Intelligence - Oncology / Prostate Cancer Johnson & JohnsonDirector, Data, Data Science And Artificial Intelligence - Oncology / Prostate CancerNew Brunswick, NJ$164,000–$282,900 / yearAll Job Posting Locations: Cambridge, Massachusetts, United States of America, New Brunswick, New Jersey, United States of America, Raritan, New Jersey, United States of America, San Diego, California, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America. This Director role, sitting on the Solid Tumor Oncology team, will direct and lead efforts to bring innovative Data Science approaches to late-stage Oncology Compound Development Team(s) with a specific focus on the Prostate Cancer portfolio.
Director, MEG Lead Immunology, Medical Evidence Generation Bristol Myers SquibbDirector, MEG Lead Immunology, Medical Evidence GenerationPrinceton, NJ$207,490–$251,433 / yearDirector of Medical Evidence Generation in Medical Affairs, will lead strategy, development, and execution of robust evidence generation strategies for the Neuroscience portfolio through Clinical Research Collaborations (CRCs), Medical Affairs Sponsored Studies (MAST), and Investigator-Sponsored Research Studies (ISRs), designed to inform clinical development, support product value, and underpin medical strategy across the product lifecycle. Responsibilities will include, but are not limited to, the following: Define and drive the integrated evidence generation strategy (IEP) aligned with Medical Affairs and overall product strategy, spanning clinical trials (Phase II/IV), real-world evidence (RWE), non-interventional studies, registries, observational research, and health outcomes studies.
Lcsw/Lmsw Deputy Director, Elder Reentry Initiative Osborne AssociationLcsw/Lmsw Deputy Director, Elder Reentry InitiativeBronx, NY$93,000–$97,000 / yearReporting directly to the VP of Prison Services, you will oversee daily program operations, ensure all contractual obligations are met, and manage a team of seven dedicated staff members, including a Clinical Social Worker, Reentry Care Managers, a Program Assistant, Peer Mentors, and social work interns. Maintain strong working relationships with Department of Corrections (DOC) and Department of Corrections and Community Supervision (DOCCS) partners, community supervision agencies, funders, partners, and community members.
Senior Director, Mavacamten Medical Product Lead Bristol Myers SquibbSenior Director, Mavacamten Medical Product LeadPrinceton, NJ$229,380–$277,956 / yearThe Senior Director, MPL will have oversight over the Mavacamten asset across the full spectrum of hypertrophic cardiomyopathy (HCM) indications - both obstructive (oHCM) and non-obstructive (nHCM) - and related life cycle management opportunities, and should be able to direct and navigate complex issues across the broad cross-functional matrixed partners to ensure optimal medical affairs strategy is developed and executed. Establish and oversee global medical data generation strategies; collaborate with Medical Evidence Generation (MEG) to oversee the execution of Investigator Sponsored Research (ISR) programs for Mavacamten from concept through full execution, including reporting at scientific congresses, in peer-reviewed publications, and through proactive/reactive BMS communication tools.
Associate Director, Quality Risk Specialist (Gcp) Bristol Myers SquibbAssociate Director, Quality Risk Specialist (Gcp)Princeton LVL, NJ$175,310–$212,438 / yearProject Management: Must be able to manage complex assignments/projects and effectively deliver all expected deliverables in a timely manner and proactively communicate changes in pre-established goals and deadlines. The Associate Director, RBQM will mainly be responsible for developing the Quality Narrative at the study and/or ASSET and TA levels to document end-to-end RBQM for critical to quality (CtQ) data, processes, and vendors, demonstrating effective risk and issue management.
Director, Medical Safety Assessment Physician, Neuroscience Bristol Myers SquibbDirector, Medical Safety Assessment Physician, NeurosciencePrinceton, NJ$286,560–$347,244 / yearOversee, prepare and/or review aggregate safety review documents (eg, Development Safety Update Reports [DSUR], Periodic Benefit-Risk Evaluation Reports [PBRER]) and safety sections of relevant clinical trial documents (eg, protocols, clinical study reports [CSR], investigator brochures [IB], informed consent forms [ICF]) and regulatory filings (eg, clinical trial applications [CTA], marketing authorization applications [MAA]). Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
R1603608 Director, Global Health Economics And Outcomes Research (Heor), Neuroscience Bristol Myers SquibbR1603608 Director, Global Health Economics And Outcomes Research (Heor), NeurosciencePrinceton, NJ$211,880–$256,748 / yearBased on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
NewSr. Medical Director-Affordability Medical Cost Optimization Blue Cross and Blue Shield AssociationSr. Medical Director-Affordability Medical Cost OptimizationNewark, NJ$240,200–$334,110 / yearPartner with leadership across Horizon BCBSNJ business units to identify MCO opportunities and drive progress toward operational process improvements to ensure continual, measurable improvement of the quality, compliance, and speed of execution of MCO initiatives. This compensation range is specific to the job level and takes into account the wide range of factors that are considered in making compensation decisions, including but not limited to: education, experience, licensure, certifications, geographic location, and internal equity.
Director, WW Cell Therapy Portfolio, Class Expansion And ST Pipeline Bristol Myers SquibbDirector, WW Cell Therapy Portfolio, Class Expansion And ST PipelinePrinceton, NJ$204,200–$247,437 / yearReporting to the Sr Director, the Director, WW Cell Therapy Class Expansion & Solid Tumor (ST) Pipeline serves as a global medical leader responsible for driving CAR-T class expansion strategy across hematology and autoimmune disease and shaping early-stage solid tumor pipeline medical strategy. Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
Director, Analytics Welbe Health LLCDirector, AnalyticsNY$159,939.07–$211,119.57 / yearThis role will interact with various functional leaders in understanding their unique business problems (e.g., how to reduce attrition, improve clinical interventions, optimize transport times, reduce unhelpful utilization, maximize real estate efficiency, simplify operational workflows, increase member and employee satisfaction etc.), analyze available enterprise and external data and develop analytical models to uncover levers that could be applied to improve business outcomes. This role is different because the Director, Analytics at WelbeHealth: Serves as a strategic thought partner to executive, operational, and clinical leaders, applying advanced analytics, modeling, and data-driven insights to solve complex business challenges that directly improve participant outcomes, operational performance, and organizational growth.
Director, Data, Data Science and Artificial Intelligence - Oncology / Prostate Cancer Johnson & JohnsonDirector, Data, Data Science and Artificial Intelligence - Oncology / Prostate CancerNew Brunswick, NJ$164,000–$282,900 / yearAll Job Posting Locations: Cambridge, Massachusetts, United States of America, New Brunswick, New Jersey, United States of America, Raritan, New Jersey, United States of America, San Diego, California, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America. This Director role, sitting on the Solid Tumor Oncology team, will direct and lead efforts to bring innovative Data Science approaches to late-stage Oncology Compound Development Team(s) with a specific focus on the Prostate Cancer portfolio.
Senior Director, Pharmacology Formation Bio IncSenior Director, PharmacologyNew York, NY$285,000–$400,000 / yearPhD in Pharmacology or a related field with at least 10 years of experience in the biopharmaceutical industry Proven track record in leading pharmacology efforts in late-stage drug development Strong understanding of regulatory requirements for pharmacology studies in support of clinical development Experience in due diligence activities for in-licensing opportunities Excellent communication and leadership skills Ability to work effectively in a fast-paced, cross-functional environment Innovative mindset and enthusiasm for leveraging technology in drug development Thorough knowledge and understanding of drug development and clinical research concepts, practices, and regulations Critical thinker about the legacy assumptions in the clinical research process and able to reimagine processes from the ground up Embraces open conversations and challenges to status quo thinking Solid written and oral communication skills; able to synthesize complex concepts and deliver messages clearly Extensive experience in scientific and clinical due diligence for late-stage assets in therapeutic areas that include metabolic and dermatological conditions Experience interacting with regulatory agencies and familiarity with regulatory requirements for dermatology indications Innovative mindset and enthusiasm for leveraging technology to transform drug development in dermatology. Recognizing that this development bottleneck may ultimately limit the number of new medicines that can reach patients, Formation Bio, founded in 2016 as TrialSpark Inc., has built technology platforms, processes, and capabilities to accelerate all aspects of drug development and clinical trials.
Director, Pharmacovigilance Scientist Bristol Myers SquibbDirector, Pharmacovigilance ScientistPrinceton, NJ$217,520–$263,577 / yearRisk Management Planning & Execution: Creates strategy for creation and update of the EDSR to proactively characterize emerging safety concerns during asset development, support Structured Benefit Risk, and define the strategy for Company Core Risk Management and gaining alignment with SMT/governance, including collaboration with Epidemiology on risk minimization effectiveness, non-interventional research (NIR) activities for post-authorization safety studies (PASS). The Director, Patient Safety Scientist, is a key partner and strategic advisor to Medical Safety Assessment Physician (MSAP)/Safety Management Team (SMT) Chair to characterize conditions for safe use of BMS medicines and proactively communicate safety evidence to influence decision-making for assets in development and marketed products by evaluating and mitigating risks.
Director, WW Cell Therapy Portfolio, Class Expansion and ST Pipeline Bristol-Myers Squibb CoDirector, WW Cell Therapy Portfolio, Class Expansion and ST PipelinePrinceton, NJ$204,200–$247,437 / yearReporting to the Sr Director, the Director, WW Cell Therapy Class Expansion & Solid Tumor (ST) Pipeline serves as a global medical leader responsible for driving CAR-T class expansion strategy across hematology and autoimmune disease and shaping early-stage solid tumor pipeline medical strategy. Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
Director GHEOR Neuroscience Bristol-Myers Squibb CoDirector GHEOR NeurosciencePrinceton, NJ$211,880–$256,748 / yearBased on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
Director of GTM Narrative Maven Clinic coDirector of GTM NarrativeNY$180,000–$210,000 / yearYou will define the core company-level narrative frameworks that anchor our go-to-market efforts, ensuring that narrative is expressed consistently across key touchpoints, including corporate pitch decks, landing pages, and campaign materials. Your job is to ensure one coherent company-level narrative across enterprise sales, enrollment marketing, and new product launches, as well as support brand campaigns and major company moments with the rest of the brand and communications team.
Senior Director, Scientific Affairs Rochester Regional Health SystemSenior Director, Scientific AffairsNY$175,000–$240,000 / yearServing as the internal and external scientific ambassador for ACM, the role partners closely with senior leadership, clients, and industry stakeholders to identify gaps, develop innovative scientific solutions, and strengthen service offerings. This role provides strategic scientific leadership to advance ACM's long-term vision, translating organizational strategy into high-impact scientific execution across global teams of scientists, PhDs, and R&D professionals.
Senior Director, Scientific Affairs ACM Global Central Laboratory LtdSenior Director, Scientific AffairsNY$175,000–$240,000 / yearThis role provides strategic scientific leadership to advance ACMs long-term vision, translating organizational strategy into high-impact scientific execution across global teams of scientists, PhDs, and R&D professionals. Serving as the internal and external scientific ambassador for ACM, the role partners closely with senior leadership, clients, and industry stakeholders to identify gaps, develop innovative scientific solutions, and strengthen service offerings.
Associate Director Preclinical & Translational PK/PD Regeneron Pharmaceuticals IncAssociate Director Preclinical & Translational PK/PDNY$176,100–$287,300 / yearThe Associate Director of Translational/Preclinical Modeling develops and implements quantitative and mechanistic PK/PD models to aid in the understanding of target biology, therapeutic modality selection/optimization, and contributes to early clinical trial dose selection and/or design and advancement and strategic direction of modeling and simulation sciences. A Typical Day May Include: Independently develops and implements quantitative and mechanistic mathematical PK/PD models that inform preclinical-to-early clinical translation, including human efficacious dose predictions and first-in-human dose selection.
Director, Health Economics & Outcome Research Integra LifeSciences Holdings CorpDirector, Health Economics & Outcome ResearchPrinceton, NJ$145,000–$199,000 / yearThis leader will generate and translate robust economic and real-world evidence to demonstrate the clinical, financial, and system-level value of Integra's technologies across priority therapeutic areas, including but not limited to Surgical Reconstruction, Advanced Wound Care, Neurosurgery, ENT, Regenerative Technologies]. Reporting to the Global Head of Market Access, this role shapes and executes the company's health economics and outcomes research (HEOR) strategy to enable reimbursement, accelerate adoption, and strengthen competitive differentiation.
Director Precision Medicine Regeneron Pharmaceuticals IncDirector Precision MedicineArmonk, NY$205,000–$341,600 / yearA typical day may include: Enhancing our understanding of indications at a cellular and molecular level Conducting novel biomarker discovery, qualifying new biomarkers/approaches to expedite proof-of-concept for new drug candidates Optimizing label claims for later stage candidates, enabling personalized medicine principles to be applied, as appropriate, in full development. This role may be for you if you have experience with the following: TA--level lead for implementation of strategic vision for clinical biomarkers in one or more therapeutic areas across multiple programs with multiple studies that will broadly enable advances in target identification, indication selection, early indication of biological activity and patient stratification/selection.
Associate Director, Field Medical Affairs- Allergy (eastern states) Regeneron Pharmaceuticals IncAssociate Director, Field Medical Affairs- Allergy (eastern states)NY$176,100–$287,300 / yearAs an Associate Director, Field Medical Affairs, you will serve as the primary scientific presence in your territory, engaging in meaningful exchange of clinical data and medical information with KOLs, HCPs, clinical research investigators, pharmacists, and other decision makers. Responding to requests for information related to study indications, disease states, and the therapeutic area, and discussing scientific and clinical data with appropriate audiences in a compliant manner.
Associate Director Quantitative Pharmacology Regeneron Pharmaceuticals IncAssociate Director Quantitative PharmacologyNY$176,100–$287,300 / yearA day in the life of an Associate Director may look like: Driving model-informed development (MIDD) and pharmacometrics strategies in partnership with Clinical Pharmacology, Biostatistics, Clinical and Translational teams to support regulatory and clinical decision-making. Demonstrated expertise in population PK/PD, exposure-response, or mechanistic modeling (systems biology, or QSP) using tools such as NONMEM, Monolix, Simulx, MATLAB/Simbiology and R.
Associate Director Statistical Programming - Pharmacometrics Regeneron Pharmaceuticals IncAssociate Director Statistical Programming - PharmacometricsNY$176,100–$287,300 / yearThe incumbent is responsible for addressing administrative functions required for project management such as compilation of resource requirements and milestones, identifying/communicating changes in project requirements that may affect key deliverables at the project level, and working with the department head to develop resource strategies. Comprehensive understanding of biostatistics, pharmaceutical clinical development (i.e. safety deliverables, efficacy analysis), experienced in data handling, process and analysis and able to understand/perform Pharmacokinetics, immunogenicity, exposure response analysis in timely manner.
Medical Director Heyday Wellness LLCMedical DirectorBrooklyn, NY$1,000–$4,000With over 1 million facials performed over the past ten years, weve proven that personalized skincare and consistency are key to unlocking progress. Responsibilities include supervising medical-grade enhancements like dermaplaning, ensuring compliance with state and local guidelines, and providing timely sign-offs on procedures.
Global Medical Director, Sleep Disorders - Neurology Global Medical Affairs Eisai IncGlobal Medical Director, Sleep Disorders - Neurology Global Medical AffairsNutley, NJUnder VP, Head of Neurology Global Medical Affairs, this role will be responsible for working with key stakeholders (clinical development team, regional medical affairs teams, global commercial/product franchise team, global value & access team as well as external KOLs) to develop and execute medical affairs strategy and priorities in the short and long term. The Medical Director will utilize expert medical/scientific knowledge in sleep disorders and orexin biology to provide strategic input for the development of product strategies and liaise with external and internal stakeholders and strengthen Eisai's medical reputation in the sleep disorders community.
Director HEOR Strategy - Aesthetics AbbVie IncDirector HEOR Strategy - AestheticsFlorham Park, NJMust be able to develop creative and effective solutions to inter- and intra-project priority conflicts, resource constraints and other problems which may impact project or group goals and deliverables across multiple programs. Purpose: AbbVie seeks a Director for the Aesthetics & Regenerative Medicine HEOR-Strategy team to lead strategic research for pipeline and on-market products, supporting approval, reimbursement, and differentiation.
Associate Director, Biostatistics - Genetic Medicine Regeneron Pharmaceuticals IncAssociate Director, Biostatistics - Genetic MedicineNY$176,100–$287,300 / yearIn this role, a typical day might include: The incumbent will lead efforts of the Biostatistics department with cross-functional teams to articulate drug development questions, assess the feasibility of endpoints and frame statistical approaches to address those questions, design clinical experiments and interventional studies to generate and analyze the resulting data, and work with teams to appropriately interpret the results and make decisions. Lead contributions to the preparation of material to be used in regulatory interactions, including drafting analysis plan and reviewing TFLs to be used in regulatory meetings, slides for advisory committee meetings, etc.
DIRECTOR CLINICAL RISK MANAGEMENT - QUALITY & PATIENT SAFETY - FULL-TIME DAY SHIFT (25480) Bergen New Bridge Medical CenterDIRECTOR CLINICAL RISK MANAGEMENT - QUALITY & PATIENT SAFETY - FULL-TIME DAY SHIFT (25480)Paramus, New JerseyThe Director of Clinical Risk Management leads efforts to minimize patient/resident harm, financial loss, and legal liability in healthcare by managing risk programs, investigating adverse events, analyzing data, ensuring regulatory compliance (including TJC, CMS), providing staff education on patient safety, and collaborating with legal/leadership on incidents, RCA, FMEA, and quality improvement to foster a strong safety culture. Incident Investigation & Analysis: Lead investigations of adverse events, analyze incident reports (UORs), conduct Root Cause Analyses (RCAs) and Failure Mode and Effect Analyses (FMEAs) to identify systemic issues.
NewDirector, US Marketing, Inborn Errors of the Metabolism Ultragenyx Pharmaceutical IncDirector, US Marketing, Inborn Errors of the MetabolismNYRemote$220,200–$272,100 / yearThe Director is responsible for the implementation of the brand strategy and corresponding tactics for the ongoing commercialization of both brands The successful individual will work cross-functionally with Medical Affairs, Global Brand Strategy, Marketing Research, Market Access, Patient Services, Regulatory, Legal, Compliance, Clinical Development, and Supply Chain and will work with other members of the commercial services team as needed. The Director will lead the development and execution of best-in-class annual marketing plans inclusive of market conditioning and development, disease education, brand strategies and tactical plans utilizing deep marketing knowledge and former successful metabolic rare disease & biopharmaceutical marketing experience.
Director, Translational Science (Neurology) EisaiDirector, Translational Science (Neurology)Nutley, NJThis position is designed to complement existing expertise in Alzheimer’s disease by bringing deep knowledge in non-Alzheimer’s neurodegenerative disorders, including Parkinson’s disease, Lewy body dementia, primary tauopathies, and sleep-related neurobiology. The Director of Translational Science is a scientifically driven leader who contributes to and drives the execution of integrated translational strategies across neurology programs spanning discovery through early clinical development.
Associate Director, Translational Science (Neurology) EisaiAssociate Director, Translational Science (Neurology)Nutley, New JerseyThis position provides an opportunity to develop deep expertise in neurodegenerative disease biology, including non-Alzheimer’s indications such as Parkinson’s disease, Lewy body dementia, primary tauopathies, and sleep-related disorders, while working closely with senior translational leaders. E-Verify is an Internet based system operated by the Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment eligibility of all new hires in the United States.
Medical Director, Pediatric Neurology Program The Valley HospitalMedical Director, Pediatric Neurology ProgramParamus, New Jersey$250,000–$270,000 / yearIn this position, you will be part of a larger multi-specialty group including experienced providers in Endocrinology, Developmental Pediatrics, Gastroenterology and Nutrition, Pulmonary and Sleep Medicine, Food Allergy, Cardiology, and PM&R, all in collaboration with the Mount Sinai Kravis Children’s Hospital and the Mount Sinai Health System. The Icahn School of Medicine is one of three medical schools that have earned distinction by multiple indicators: ranked in the top 20 by U.S. News & World Report's "Best Medical Schools," aligned with a U.S. News & World Report "Honor Roll" Hospital, and No. 14 in the nation for National Institutes of Health funding.
Director, Value Based Care RockstarDirector, Value Based CareNew York, NY$150,000–$175,000 / yearBy providing tailored products and services within a supportive setting, the organization is building a large national network of practitioner-owned practices, driving better outcomes for patients and communities. By providing NPs with tailored products and services within a supportive setting, it is building the nation’s largest network of NP-owned practices, driving better outcomes for patients and communities.
Medical Director, Developmental Pediatrics Program The Valley HospitalMedical Director, Developmental Pediatrics ProgramParamus, New Jersey$204,000–$219,000 / yearIn this position you will be part of a larger multi-specialty group including experienced providers in Endocrinology, Gastroenterology and Nutrition, Pulmonary and Sleep medicine, Food Allergy, Cardiology, PM&R, and Neonatology all in collaboration with Mount Sinai Kravis Children’s Hospital and the Mount Sinai Health System. The Director would lead a team including a physician, nurse practitioner and social workers to provide clinical expertise in early childhood development, behavioral, and psychosocial issues at the Kireker Center for Child Development (KCCD).
Director of Compliance and Quality Assurance Children's Aid Job ListingDirector of Compliance and Quality AssuranceNew York, New YorkThe Director ensures full compliance with New York State Department of Health (NYSDOH) and New York State Office of Mental Health (OMH) regulatory requirements for Article 28 Diagnostic and Treatment Centers, Article 29I Health Facilities, and Article 31 Mental Health Clinics, as well as federal requirements under Title X and Patient-Centered Medical Home (PCMH), while advancing a culture of quality, patient safety, and continuous improvement. Reporting to the Vice President of Health Services, the Director of Compliance & Quality Assurance is accountable for regulatory compliance, accreditation readiness, quality improvement initiatives, risk mitigation, performance monitoring, and the development of systems that promote high-quality, safe, and effective patient care across all Health Services programs.
Mental Health Assoc - Psych Child St. Clare's - BoontonMental Health Assoc - Psych ChildBoonton Township, New Jersey$20–$27 / hourSaint Clare's Health includes CMS 5-Star Rated hospitals and is an award-winning provider of safe, high quality, compassionate care, serving the communities of Morris, Warren and Sussex counties. Utilizes education to provide designated group modality to patients and individual observations to assigned patients to assist them to learn new coping skills, identify issues that cause conflict in relationships and develop strategies for resolving conflicts.
RN Supervisor - Internal Medicine and Cardiology UnitedHealth Group IncRN Supervisor - Internal Medicine and CardiologyLake Success, NY$72,800–$130,000 / yearThe fraudulent LinkedIn messages and emails, which do not originate from any Executives LinkedIn account or of UnitedHealth Group's email domains, or those of any of its operating divisions, supposedly conducts an interview via a Zoom meeting, offers a work from home job at Optum, emails an application, sends a fake check by next day delivery through USPS and asks recipients to pay a vendor a large dollar amount. Develops and maintains collaborative relationships with all members of the healthcare delivery system assisting physicians with their in baskets and making patient calls when needed.