Associate Director, Global Medical Affairs Execution 6085-Janssen Global Services Legal EntityAssociate Director, Global Medical Affairs ExecutionRaritan, New JerseyAnalytical Reasoning, Clinical Research and Regulations, Clinical Trials Operations, Communication, Content Evaluation, Developing Others, Digital Culture, Digital Literacy, Healthcare Trends, Inclusive Leadership, Leadership, Medical Affairs, Medical Communications, Medical Compliance, Prioritization of Tasks, Product Strategies, Scientific Research, Strategic Thinking, Team Management . Responsibilities : Leading the development and implementation of Global Medical Affairs strategic business priorities, partnering cross-functionally and cross-regionally with functional business leaders to ensure alignment and sustainable implementation.
Associate Surgical Account Manager/Surgical Account Manager - California 6942-ABIOMED Legal EntityAssociate Surgical Account Manager/Surgical Account Manager - CaliforniaCherry Hill, New JerseyBusiness Development, Communication, Customer Centricity, Customer Retentions, Execution Focus, Healthcare Trends, Market Knowledge, Market Research, Presentation Design, Problem Solving, Sales, Solutions Selling, Stakeholder Engagement, Strategic Sales Planning, Sustainable Procurement, Team Management, Vendor Selection Benefit Information: Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.
Associate Surgical Account Manager/Surgical Account Manager - Upstate New York 6942-ABIOMED Legal EntityAssociate Surgical Account Manager/Surgical Account Manager - Upstate New YorkCherry Hill, New Jersey$75,000–$100,000 / yearBusiness Development, Communication, Customer Centricity, Customer Retentions, Execution Focus, Healthcare Trends, Market Knowledge, Market Research, Presentation Design, Problem Solving, Sales, Solutions Selling, Stakeholder Engagement, Strategic Sales Planning, Sustainable Procurement, Team Management, Vendor Selection Albany, New York, United States of America, Buffalo, New York, United States, Danvers, Massachusetts, United States of America, Horseheads, New York, United States of America, Rochester, New York, United States Job Description:
Associate Area Manager or Area Manager (Albuquerque, NM) - Johnson & Johnson MedTech, Heart Recoverych – Heart Recovery 6942-ABIOMED Legal EntityAssociate Area Manager or Area Manager (Albuquerque, NM) - Johnson & Johnson MedTech, Heart Recoverych – Heart RecoveryCherry Hill, New JerseyAccount Management, Analytical Reasoning, Business Behavior, Collaboration, Cultural Competence, Customer Analytics, Customer Centricity, Healthcare Trends, Learning Agility, Market Knowledge, Market Research, Oracle Customer Data Management (CDM), Problem Solving, Sales, Solutions Selling, Sustainable Procurement, Vendor Selection To be successful in your role you will need advanced knowledge in interventional cardiology, strong sales skills, and business savvy partnered with leadership and training skills that promote trust, respect and are backed by honor and integrity.
Associate Veterinarian Heart + PawAssociate VeterinarianNew Milford, New Jersey$100,000–$150,000 / yearFounded on the belief that veterinary professionals deserve a workplace where they can thrive and be happy, healthy, and successful, Heart + Paw offers full-service veterinary centers that are reimagining pet care in every way, providing state-of-the-art care that today's pet parents expect. Our veterinary center is ideal for veterinarians who prioritize client-centered care, value the human-animal bond, embrace low-stress handling techniques, and are committed to making a positive impact in their communities.
Associate Director Biostatistics Integrated Resources, IncAssociate Director BiostatisticsWoodcliff Lake, New JerseyFull timeExperience contributing to sensitivity analysis for missing data, longitudinal data analysis and statistical modeling diagnosticsExperience with Bayesian study designs is an added advantageExcellent interpersonal skills in project management, collaboration and communication to leadership, Study Directors, Data Management, Statistical Programming and other clinical development team members, colleagues, CROs, and external collaboratorsMust be flexible to work in a dynamic environment where multi-tasking and changing priorities existMust possess strong analytical skills in addition to demonstrated problem solving and risk mitigation skillsRecognized in the profession as a dedicated professional with a strong work ethicMust be a self-sufficient, highly motivated, highly organized, and proactive individual who is a quick learner. Responsibilities include but are not limited to:Reviewing whole protocols and interfacing with clinicians and other functions to understand study requirements and design study elements including sample size calculations, analysis methods, study duration, etc. for multiple studiesDeveloping and/or reviewing statistical documents for multiple clinical trials, including SAPs, TLG shells and specification variable derivationDeveloping Study Quality Surveillance Plan and monitoring study conduct to proactively address issues to ensure high quality study data.
Associate Scientific Director MJH Life SciencesAssociate Scientific DirectorCranbury, New Jersey$100,000–$115,000 / yearAnalyze and apply evidence-based medical literature, clinical practice guidelines, and disease-state knowledge across various diseases—evaluating levels of evidence, interpreting clinical trial data, assessing therapeutic options, identifying unmet needs, and developing product-specific education. Serve as a subject matter expert in support of business development efforts; collaborate with sales teams to identify and present opportunities for funded projects and programs, and contribute to project management activities as needed.
Associate Director, Toxicology Protagonist TherapeuticsAssociate Director, ToxicologyNewark, New JerseyThe Company also has a number of preclinical stage drug discovery programs addressing clinically and commercially validated targets including an oral IL-17 peptide antagonist, obesity dual and triple agonists, an oral hepcidin functional mimetic, and the recently announced IL-4 and amylin programs. Associate Director, Toxicology, Nonclinical Development (Program Toxicologist) Position Description: Protagonist Therapeutics is seeking a talented, highly motivated professional to join the Toxicology, Nonclinical Development team as Associate Director Toxicology, Nonclinical Development (Program Toxicologist).
Associate Director, Global Data Management and Standards - Business Operations Merck & Co IncAssociate Director, Global Data Management and Standards - Business OperationsRahway, NJThe Associate Director partners with business leaders and key stakeholders to lead change management efforts, develop and execute communication strategies that promote transparency and stakeholder engagement, and champion learning and development initiatives that build organizational capabilities and support adoption of new processes, technologies, and ways of working. Responsibilities: Forecasting, Capacity, & Portfolio Management: Maintain headcount, workload, and demand models for the functional area; run allocation algorithms to help ensure the Book of Business is delivered with quality and timeliness.
Associate Director, Laboratory Operations, Logistics and Safety Compliance (Onsite) Merck & Co IncAssociate Director, Laboratory Operations, Logistics and Safety Compliance (Onsite)Rahway, NJ$142,400–$224,100 / yearThe successful candidate will bring strong prior experience in device-focused laboratory environments performing development and fit-for-purpose activities for clinical supply, including engineering labs, testing labs, and human factors/usability spaces, along with deep expertise in EHS and inspection readiness. Required Skills: Biological Sciences, Design Thinking, Design Verification, Electronics Prototyping, Environmental Health And Safety, Laboratory Maintenance, Leading Project Teams, Life Science, Manufacturing Methodologies, Occupational Safety and Health, People Management, Product Development Design, Regulatory Compliance, Regulatory Inspections, Safety Compliance.
Associate Director, Translational Science (Neurology) Eisai USAssociate Director, Translational Science (Neurology)Nutley, NJThis 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.
Associate Director, Business Development ACADIA PHARMACEUTICALS INCAssociate Director, Business DevelopmentPrinceton, NJ$158,200–$197,800 / yearRole supports and coordinates activities related to the search, identification, competitive intelligence, and business case for potential transactions, working with the External Innovation and Commercial teams who lead the scientific and commercial assessments, which are incorporated into the overall deal package by BD.- Performs in-depth evaluations, interpreting competitive landscape and analysis of financial data.- Stays abreast of emerging healthcare & pharmaceutical industry trends and assess their potential impact on business strategies.*Education/Experience/Skills:*Targeting a minimum of 5 years of progressively responsible experience within consulting, venture capital or investment banking with a focus on valuation of and strategic transactions related to of therapeutics/companies in the pharmaceutical or biotech industry.
Business Development Associate ArdenaBusiness Development AssociateSomerset, New JerseyArdena provides integrated services spanning drug substance development, drug product formulation, GMP manufacturing, bioanalytical services, clinical logistics, fill and finish, and CMC regulatory support. Ardena offers an international working environment where employees are encouraged to develop their expertise, take ownership, and grow their careers across functions and locations.
Global Labelling Associate Director, Content (Cardiovascular, Renal & Metabolism) Novartis AGGlobal Labelling Associate Director, Content (Cardiovascular, Renal & Metabolism)East Hanover, NJExpected Annual Base Salary Range for role: €75,880 to €140,920 The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. Working at the intersection of science, strategy, and regulatory excellence, you will lead the development of high-quality global labelling content that supports patient safety, regulatory compliance, and commercial success.
Global Labelling Associate Director, Content (Oncology) Novartis AGGlobal Labelling Associate Director, Content (Oncology)East Hanover, NJExpected Annual Base Salary Range for role: €75,880 to €140,920 The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. Working at the intersection of science, strategy, and regulatory excellence, you will lead the development of high-quality global labelling content that supports patient safety, regulatory compliance, and commercial success.
Associate Director, Translational Science (Neurology) EisaiAssociate Director, Translational Science (Neurology)Nutley, NJThis 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.
Associate Director - Data Standards Hybrid AbbVie IncAssociate Director - Data Standards HybridFlorham Park, NJApplicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
Associate Director, Translational Science (Neurology) Eisai IncAssociate Director, Translational Science (Neurology)Nutley, NJThis 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.
Associate Dir, Full Stack Data Scientist Bayer AGAssociate Dir, Full Stack Data ScientistWhippany, NJ$131,600–$197,400 / yearYOUR TASKS AND RESPONSIBILITIES: Accountable to ensure the entire DS capabilities stack for the assigned process, and tasks are effective, efficient and meeting business operational needs; Hands on development of capabilities as required by the initiatives, mission leads, and product owners and other DSAI accountable parties; Identify business technology developments in the industry early on and actively promote them within the organization; Responsible for providing conceptual guidance to team members in appropriately designing certain capabilities as required to support the DSAI Analytics strategy; Ensure assigned business process area technology needs are met by interfacing and collaborating with the R&D functions; preparing and supporting delivery of DS capabilities and roadmaps in close collaboration with Head of DDRC and DSAI sub-clusters; Accountable to ensure process area capability issues are assessed upstream and downstream, communicated, coordinated and resolved promptly; Design, develop, and maintain full stack applications to support R&D initiatives; Collaborate with data scientists, ML engineers, and domain experts to translate research prototypes into production-ready tools; Build intuitive user interfaces and robust backend systems for data visualization, model interaction, and experimentation; Develop APIs and microservices to integrate with internal platforms and external data sources; Optimize performance, scalability, and reliability of R&D tools and applications; Participate in architectural discussions and contribute to technical strategy for R&D software infrastructure; Rapidly prototype new ideas and iterate based on feedback from researchers and stakeholders. Knowledge of database systems: such as SQL (PostgreSQL, MySQL) and NoSQL (MongoDB, Redis); Ability to work in a collaborative, interdisciplinary team environment; Experienced in GxP/CSV & IT project and/or business process design; Extensive experience in Data Science capability assessment and analysis; Demonstrated ability to address and resolve conflicts; proven collaboration skills; Pharma and life sciences domain experience; Applicable security and compliance experience; Exposure to machine learning workflows or experience integrating ML models into applications; Experience with data visualization libraries (D3.js, Plotly, etc.); Understanding of MLOps or model deployment practices; Background in scientific computing, data engineering, or experimental software development; Demonstrated ability to lead through influence working in a cross functional team, building relationships with engineering teams and business stakeholders; Passion for digital transformation, change in general and play to win mentality; Preferred Qualifications: Project management experience is preferred.
Associate Principal Scientist - ADME Just-Evotec BiologicsAssociate Principal Scientist - ADMEPrinceton, New JerseyAbility to perform high-impact as well as high throughput studies to completion in a fast paced environment, while managing multiple projects to meet the timelines. Provides scientific knowledge and responsible in establishing new TOX assays as well as contribute to the continuous improvement of the current TOX assays.
NewAssociate Principal Scientist - In Vitro Toxicology - Microelectrode Array - Site Based, Princeton, NJ Just-Evotec BiologicsAssociate Principal Scientist - In Vitro Toxicology - Microelectrode Array - Site Based, Princeton, NJPrinceton, New JerseyAbility to perform high-impact as well as high throughput studies to completion in a fast paced environment, while managing multiple projects to meet the timelines. Provides scientific knowledge and responsible in establishing new TOX assays as well as contribute to the continuous improvement of the current TOX assays.
Associate Principal Scientist, Process Chemistry Merck & Co IncAssociate Principal Scientist, Process ChemistryRahway, NJ$142,400–$224,100 / yearRequired Skills: Analytical Chemistry, Analytical Development, Chemical Processes, Chemical Processing, Chemical Products, Chemical Synthesis, Clinical Judgment, Computational Chemistry, Data Analysis, Enzymology, Evidence Based Decision Making, Experimental Development, Lead Optimization, Molecular Structure, Multidisciplinary Collaboration, Organic Chemistry, Synthetic Chemistry, Technology Transfer, US Patent. Responsibilities include identifying and implementing enabling technologies, solving complex chemistry challenges, leading cross-functional collaborations, supporting technology transfers, and mentoring junior scientists.
Associate Principal Engineer, Drug-Device Combination Products Merck & Co IncAssociate Principal Engineer, Drug-Device Combination ProductsRahway, NJ$142,400–$224,100 / yearRequired Skills: CAD Modeling, Combination Products, Computer-Aided Design (CAD), Design Controls, Design Failure Mode and Effect Analysis (DFMEA), Design Verification Testing, Device Development, Human Factor Engineering, Machine Learning (ML), Medical Device Management, Medical Device Manufacturing, Medical Device Quality Systems, Medical Devices Design, Quality Management Systems (QMS), Risk Control, Test Method Validation. In addition, this position shall interrogate device supplier processes as they relate to our company's combination product process specifications and critical quality attributes to support our company's combination product quality control strategy and preserve essential performance requirements.
Associate Director, Medical Writing - Neuroscience Integrated Resources, IncAssociate Director, Medical Writing - NeuroscienceWoodcliff Lake, New JerseyFull timeAssociate Director, Medical Writing - NeuroscienceThe Associate Director - Medical Writing will be the designated Lead Medical Writer for approximately 3 Neuroscience or General Medicine Programs, responsible for providing needed support and direction to other staff/contractors on these programs. As the lead writer, the incumbent ensures timely completion, accuracy and quality of all clinical and submission documentation across all aspects of the compounds' life cycle management.
Sales Associate Integrated Resources, IncSales AssociateSomerville, New JerseyFull timeJob Description• Meeting with customers over the phone, email, or on site to assist in business development• Maintain current accounts and database• Excellent interpersonal skills, organizational skills, very detail oriented• Making presentations and demonstrating how our services can meet client needs• Managing and interpreting customer requirements - speaking with clients to understand, anticipate and meet their needs• Attending and/or participating in trade shows, conferences and other marketing events• Searching for new clients who might benefit from our company services• Cold calling, generating new leads, prospecting, and converting them into new clientsQualifications• Excellent oral and written communication skills• Excellent interpersonal skills• Experience in a technical sales is a plus• Knowledge of metrology services is a plus• Associates or bachelor's degree in business/sciences/engineering• 0-2 years or experience in sales Sales AssociateA Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms.
Associate Director Integrated Resources, IncAssociate DirectorBridgewater, New JerseyFull timeProvide support to regulatory inspections as the primary subject matter expert• This position will specifically report to our facility in Branchburg, NJ.Qualifications• 15+ years' experience• Management Experience Required - Yes• Minimum Education - Bachelor's Degree• Willingness to Travel - Occasionally Evaluate changes to the validated state of systems through change control procedures and participate in the planning and implementation of changes• Develop and implement validation policies.
Senior Manager / Associate Director - Data Governance Tiger Analytics Inc.Senior Manager / Associate Director - Data GovernanceJersey City, NJLead pods focused on data lineage documentation (consumption through ADS to system of origin), target-state ADS landscape and architecture design, and aggregation layer controls including DQ rules, variance analysis, and anomaly detection. Conduct SME interviews across engineering and business data offices, translate enterprise data management policy into actionable delivery and build plans, and manage a small team of analysts through design and implementation.
Associate Scientific Director MJH Life Sciences Multimedia Medical LLCAssociate Scientific DirectorCranbury, NJ$100,000–$115,000 / yearAnalyze and apply evidence-based medical literature, clinical practice guidelines, and disease-state knowledge across various diseases-evaluating levels of evidence, interpreting clinical trial data, assessing therapeutic options, identifying unmet needs, and developing product-specific education. Serve as a subject matter expert in support of business development efforts; collaborate with sales teams to identify and present opportunities for funded projects and programs, and contribute to project management activities as needed.
Associate Director, Risk Based Quality Management Lead Summit Therapeutics plcAssociate Director, Risk Based Quality Management LeadPrinceton, NJServing as the primary RBQM subject matter expert within study teams, this role implements and maintains study-level risk management, centralized monitoring, Key Risk Indicators (KRIs), Quality Tolerance Limits (QTLs), targeted monitoring strategies, and risk review processes. Working closely with Clinical Operations, Clinical Science, Data Management, Biostatistics, Medical Monitoring, and CRO partners, the RBQM Lead proactively identifies, evaluates, escalates, and mitigates risks throughout the clinical trial lifecycle to support participant safety, data reliability, and regulatory compliance.
Associate Director Vendor & Relationship Management Acadia Pharmaceuticals IncAssociate Director Vendor & Relationship ManagementPrinceton, NJ$145,400–$181,700 / yearThe Associate Director, Vendor & Relationship Management will support and optimize strategic partnerships with clinical vendors, CROs, and functional service providers to ensure operational excellence, compliance, and value delivery across global clinical development programs. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs.
NewSr. Associate, Quality Operations Aequor Technologies LLCSr. Associate, Quality OperationsPrinceton, NJThis role works closely with Quality Operations and internal R&D teams across all departments such as Clinical Development, Clinical Operations, Biometrics, Regulatory Affairs, Drug Safety and Pharmacovigilance, Translational Sciences, Program Management, and Medical Affairs. Assist with inspection preparation activities, including tracking and closure of IR actions across multiple parallel workstreams, preparation of meeting minutes, scheduling of meetings, coordinating trainings, etc.
Inbound/Outbound Queue Associate - Behavioral Health CVS Health CorpInbound/Outbound Queue Associate - Behavioral HealthNJRemote$17–$31.30 / hourThis is a fully remote position and the following are some required Work from Home criteria which includes but is not limited to maintaining your own internet with approved speed requirements, secure workspace free from distractions, and successful completion of the training program. Strong customer service skills to coordinate service delivery including attention to customers, sensitivity to issues, proactive identification and resolution of issues to promote positive outcomes for members.
Strategy Insights & Planning Associate Consultant - AOR ZS Associates IncStrategy Insights & Planning Associate Consultant - AORPrinceton, NJZS's Access, Strategy & Implementation team partners with leading pharmaceutical and biotech companies to solve their most pressing market access challenges, by delivering deep expertise on topics including B2B engagement, pricing and value strategy with advanced analytics, and value narrative shaping. Distill complex clinical, economic, and health outcomes evidence into clear, persuasive written deliverables, including value propositions, messaging platforms, objection handlers, payer/provider narratives, and AMCP-style dossiers.
Associate Director Revenue Cycle & Coding Cooper University Health CareAssociate Director Revenue Cycle & CodingCamden, NJThe Associate Director leads revenue cycle initiatives across multiple surgical specialties, utilizing data analytics and process improvement methodologies to improve key performance indicators while supporting exceptional patient and provider experiences. Monitor and improve key performance metrics including charge capture, coding accuracy, accounts receivable, denial rates, clean claim rate, reimbursement, lag days, and cash collections.
Associate Director, Statistical Programming Eisai IncAssociate Director, Statistical ProgrammingNutley, NJ$200,091.38–$217,900 / yearSkills:Communication & Cross-functional Influence, Critical Thinking & Business Agility, Industry/ Regulatory Knowledge, Mentoring/ People Development, Project Management, Statistical Programming Skills, Vendor Management. Requirements: A Master's degree in Molecular and Cellular Biology, Biotechnology, or closely related plus 8 years of experience in Pharmaceutical industry experience in clinical development statistical programming methods and processes in job offered or related roles.
Associate Director of Admissions - Shreiber School of Veterinary Medicine (SSVM) of Rowan University Rowan UniversityAssociate Director of Admissions - Shreiber School of Veterinary Medicine (SSVM) of Rowan UniversityGlassboro, NJ$75,000–$95,000 / yearInformation about the institution: Rowan University is a public Carnegie-classified (R2/high research activity) institution with approximately 23,000 students offering bachelor''s through doctoral and professional degrees and has earned national recognition for innovation, commitment to high-quality, affordable education, and developing public-private partnerships. Working within the Office of Student Success, the Associate Director for Admissions will interact with various stakeholders across SSVM and Rowan University, including financial aid, registrar, and admissions offices.
Associate Director, Regulatory Affairs Project Planning & Coordination ACADIA Pharmaceuticals Inc.Associate Director, Regulatory Affairs Project Planning & CoordinationPrinceton, NJ$154,000–$193,000 / yearWe are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. The Associate Director, Regulatory Affairs Project Planning & Coordination is responsible for developing, implementing, and monitoring project plans and best practices that facilitate how the Global Regulatory Affairs department executes its strategic and functional goals.
Associate Director, Translational Program Manager (Early Development & Cell Therapy) Bristol-Myers Squibb CoAssociate Director, Translational Program Manager (Early Development & Cell Therapy)Princeton, NJ$180,430–$218,638 / yearProvide strong collaboration, coordination, and communication skills to support cross-functional interactions and prioritization of activities to meet demands across Translational Research team in line with program priorities (i.e., other translational teams, assay teams, outsourcing representatives, vendors, biospecimen leads, data management, biostatistics, operations leads and specialty testing labs, as relevant for the program and assays). Provides strategic operational leadership, including oversight of translational budgets and alliances; partners with Translational leadership to establish effective ways of working; and leads the planning and execution of cross‑functional governance forums to enable timely, high‑quality decision‑making.
NewAssociate Medical Director Johnson & JohnsonAssociate Medical DirectorTitusville, New JerseyAnalytical Reasoning, Clinical Research and Regulations, Clinical Trials Operations, Communication, Cross-Functional Collaboration, Healthcare Trends, Leverages Information, Medical Affairs, Medical Communications, Medical Compliance, Mentorship, Product Strategies, Scientific Communications, Strategic Thinking, Tactical Planning, Technical Credibility . The Associate Medical Director acts, in collaboration with CAPLYTA Medical Affairs leadership, to connect therapeutic strategy with the clinical, scientific, and operational implementation of U.S.-focused company-sponsored or investigator-initiated studies supporting CAPLYTA.
Associate Director, Camzyos Analytics Bristol Myers SquibbAssociate Director, Camzyos AnalyticsPrinceton, NJ$167,540–$203,013 / 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. As an Associate Director, this role will collaborate closely with cross-functional partners—including members of the Tumor, Sales, Medical, and Access teams—to support data-informed decision-making and customer engagement.
Associate Director, WW Lymphoma Bristol Myers SquibbAssociate Director, WW LymphomaPrinceton, NJ$167,540–$203,013 / 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. As an Associate Director, this role will collaborate closely with cross-functional partners—including members of the Tumor, Sales, Medical, and Access teams—to support data-informed decision-making and customer engagement.
Associate Director, Milvexian MR Bristol Myers SquibbAssociate Director, Milvexian MRPrinceton, NJ$167,540–$203,013 / 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. As an Associate Director, this role will collaborate closely with cross-functional partners—including members of the Tumor, Sales, Medical, and Access teams—to support data-informed decision-making and customer engagement.
Associate Director, Early Asset - Neuro Bristol Myers SquibbAssociate Director, Early Asset - NeuroPrinceton, NJ$167,540–$203,013 / 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. As an Associate Director, this role will collaborate closely with cross-functional partners—including members of the Tumor, Sales, Medical, and Access teams—to support data-informed decision-making and customer engagement.
Associate Director, NEX-T Bristol Myers SquibbAssociate Director, NEX-TPrinceton, NJ$167,540–$203,013 / 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. As an Associate Director, this role will collaborate closely with cross-functional partners—including members of the Tumor, Sales, Medical, and Access teams—to support data-informed decision-making and customer engagement.
Associate Director, Multi. Myel (Abecma + Arlo-cel) Bristol Myers SquibbAssociate Director, Multi. Myel (Abecma + Arlo-cel)Princeton, NJ$167,540–$203,013 / 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. As an Associate Director, this role will collaborate closely with cross-functional partners—including members of the Tumor, Sales, Medical, and Access teams—to support data-informed decision-making and customer engagement.
Associate Director, Inline Analytics, Neuro Bristol Myers SquibbAssociate Director, Inline Analytics, NeuroPrinceton, NJ$167,540–$203,013 / 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. As an Associate Director, this role will collaborate closely with cross-functional partners—including members of the Tumor, Sales, Medical, and Access teams—to support data-informed decision-making and customer engagement.
Associate Director Radiology - PMPH Penn MedicineAssociate Director Radiology - PMPHPlainsboro, NJ$99,906.14–$154,643.42 / yearCompliance:tEnsure continuous survey readinesstEnsure department human resource management practices comply with labor law, state & federal requirementstEmployee safetytTreats people respectfully.tEffectively manages and efficiently uses all resources.tIs open to and respects differences, ideas, and suggestions.tDoes not participate in non-productive activities of conversations.tMaintains confidentiality.tEstablishes and maintains good working relationships and partnerships.tAdheres to established policies and procedures.tAlways seeks clarity to ensure understanding, keeps work processes reasonable and simple, and balances priorities.tEffectively communicates and ensures understanding of the mission, vision, and values.tMakes and keeps commitments.tMeet deadlines and is responsive to requests.tAlways exemplifies in his/her action principles of collegiality and collaboration.tShare data with staff and mutually identify opportunities for improvement within the department's span of influence.tCollaborate with the staff to develop action plans for improvement.tImplement and follow through with action plantDrive patient/client loyalty and physician referral by ensuring staff under your supervision understand the UPHS commitment to service, their own work processes, and have the necessary skills to meet service expectationstManage patient/client complaints and provide timely follow up to ensure satisfaction.tEnsure that staff understand and demonstrate service recovery commitment. Establish/update processes and work practices for the unit/department.tBuild work practices and team processes for Improvement:1.tSafe: avoid injuries to patients from the care that is intended to help them.2.tEffective: provide services based on scientific knowledge.3.tPatient-Centered: provide care that is responsible to individual patient preferences, needs and values and assuring that patient values guide all clinical decisions.4.tTimely: reduce waits and sometimes-harmful delays for both those who receive care and those who give care.5.tEfficient: avoid waste, including waste of equipment, supplies, ideas, and energy.6.tEquitable: provide care that does not vary in quality because of personal characteristics such as gender, ethnicity, geographic location or socio- economic status.tIn conjunction with all stakeholders involved in the patient care processes, institute operational changes based on data.tCommunicate, reinforce, and update as necessary environment of care procedures, (e.g.
Decision Analytics Associate Consultant - HEOR Value and Evidence Communication ZS Associates IncDecision Analytics Associate Consultant - HEOR Value and Evidence CommunicationPrinceton, NJAs a management consulting and technology firm focused on improving life and how we live it, we transform ideas into impact by bringing together data, science, technology and human ingenuity to deliver better outcomes for all. We work with our clients to go beyond delivering high quality studies, to helping them make sure the work they are undertaking are the right ones to support their strategic priorities, and even shape those priorities.
Patient Access Associate - Emergency Department - Part Time/Evenings Penn MedicinePatient Access Associate - Emergency Department - Part Time/EveningsPlainsboro, NJ$17.75–$28.33 / hourPenn Medicine is dedicated to our tripartite mission of providing the highest level of care to patients, conducting innovative research, and educating future leaders in the field of medicine. Demonstrating and appropriately documenting out of pocket responsibility for services as related to insurance contracts or PCHS Fee Schedules Collecting time of service and point of service payments according to policy.
Patient Access Associate - Emergency Department Admissions - Full Time/ 3p - 11:30p Penn MedicinePatient Access Associate - Emergency Department Admissions - Full Time/ 3p - 11:30pPlainsboro, NJ$17.75–$28.33 / hourPenn Medicine is dedicated to our tripartite mission of providing the highest level of care to patients, conducting innovative research, and educating future leaders in the field of medicine. Demonstrating and appropriately documenting out of pocket responsibility for services as related to insurance contracts or PCHS Fee Schedules Collecting time of service and point of service payments according to policy.