Senior Quality Engineer- Medical Device- Mount Laurel, NJ Michael Page USASenior Quality Engineer- Medical Device- Mount Laurel, NJMount Laurel, NJ$110,000–$150,000 / yearFull timeThe Senior Quality Engineer will be responsible for supporting new product development in a regulated environment, with responsibility for design controls, risk management, quality systems, and regulatory compliance. With a growing market presence and ongoing investment in research, product development, and commercialization efforts, the company offers a dynamic environment for professionals seeking to make a meaningful impact in healthcare.
Senior Research Investigator, Clinical Pharmacology Bristol-Myers Squibb CoSenior Research Investigator, Clinical PharmacologyPrinceton, NJ$146,420–$177,428 / yearp>The CP&P team interacts with discovery and translational scientists, project leadership, early development, late development and commercial colleagues to optimize dosing, formulation, delivery and combination strategies to enable faster and more effective drug development informed by core scientific principals and data. 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.
Senior Research Investigator, Clinical Pharmacology & Pharmacometrics Bristol-Myers Squibb CoSenior Research Investigator, Clinical Pharmacology & PharmacometricsPrinceton, NJ$146,420–$177,428 / yearThe CP&P team interacts with discovery and translational scientists, project leadership, early development, late development and commercial colleagues to optimize dosing, formulation, delivery and combination strategies to enable faster and more effective drug development informed by core scientific principals and data. 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.
Senior Clinical Research Associate-Contractor SystimmuneSenior Clinical Research Associate-ContractorPrinceton, NJRemoteFull timeSystImmune currently has multiple assets in clinical development across solid tumor and hematologic malignancies, supported by a robust preclinical pipeline advancing novel oncology therapeutics through discovery and IND-enabling stages. The ideal candidate is a highly organized, self-motivated clinical operations professional with strong oncology monitoring experience who can work independently while collaborating effectively with cross-functional teams and external vendors.
NewSr. Clinical Research Associate SystimmuneSr. Clinical Research AssociatePrinceton, NJFull timeli style="width:6.6493in">Prepare the study reference manual, including liaising with the Contract Research Organization (CRO) team (i.e., central lab, specialty labs and vendors) to ensure efficient preparation and delivery of study materials to investigator sites. Experienced in Microsoft Office Products (Word, Excel, PowerPoint, SharePoint, Teams) and other clinical trial systems (e.g., CTMS, EDC and eTMF).
Senior Clinical Research Associate Systimmune IncSenior Clinical Research AssociatePrinceton, NJ$90,000–$130,000 / yearPrepare the study reference manual, including liaising with the Contract Research Organization (CRO) team (i.e., central lab, specialty labs and vendors) to ensure efficient preparation and delivery of study materials to investigator sites. Alongside ongoing clinical trials, SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development.
NewSr. Clinical Research Associate Systimmune IncSr. Clinical Research AssociatePrinceton, NJ$90,000–$130,000 / yearli>Prepare the study reference manual, including liaising with the Contract Research Organization (CRO) team (i.e., central lab, specialty labs and vendors) to ensure efficient preparation and delivery of study materials to investigator sites. CRA is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP guidelines, local regulations, and applicable SOPs.
Senior Clinical Research Associate-Contractor Systimmune IncSenior Clinical Research Associate-ContractorPrinceton, NJRemoteSystImmune currently has multiple assets in clinical development across solid tumor and hematologic malignancies, supported by a robust preclinical pipeline advancing novel oncology therapeutics through discovery and IND-enabling stages. The ideal candidate is a highly organized, self-motivated clinical operations professional with strong oncology monitoring experience who can work independently while collaborating effectively with cross-functional teams and external vendors.
Senior Clinical Research Associate System OneSenior Clinical Research AssociatePlainsboro Township, New Jersey$115,000–$130,000 / yearTrain and support external trial staff regarding CRF and IVRS data entry, AE/SAE/MESI reporting, ethics reporting, protocol deviation identification, drug accountability, temperature monitoring, query resolution, essential document collection, and ITF filing. Collaborate with Local Trial Manager (LTM) and Line of Business Manager, communicating site progress and escalating critical issues impacting trial milestones.
Senior Director Clinical Research Acadia Pharmaceuticals IncSenior Director Clinical ResearchPrinceton, NJ$229,100–$286,400 / 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 (Senior) Director, Clinical Research will be a highly qualified and motivated individual who will have a leadership role in the development of Acadia programs for rare diseases and/or neurologic and neuropsychiatric disorders.
Senior Clinical Research Scientist Genmab ASSenior Clinical Research ScientistPrinceton, NJFor 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. Please note that if you are applying for a position in the Netherlands, Genmab's policy for all permanently budgeted hires in NL is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the fixed-term employment contract.
Senior Research Specialist/North Carolina State Lead Princeton UniversitySenior Research Specialist/North Carolina State LeadPrinceton, NJRemote$80,000–$90,000 / yearli>Build BDI's state-based partnerships and relationships with key stakeholders representing varying sectors including election protection, racial justice, LGBTQ+ rights, faith-based, government, and others in order to provide monitoring and analysis support across the board and to better inform our research. We do this by 1) producing action-oriented and responsive research to fill existing gaps and empower local leaders; 2) enabling cross-sector collaboration, so individuals and organizations are better prepared to mitigate risk and respond to crisis when it does arise; and 3) helping to drive the policy and community response.
Senior Research Specialist Princeton UniversitySenior Research SpecialistPrinceton, NJ$60,000–$75,000 / yearThe Politics Department is seeking a Senior Research Scholar (SRS) to provide advanced research and project management support for a portfolio of research studies focused on Africa, Latin America and South Asia. The University considers factors such as (but not limited to) scope and responsibilities of the position, candidate''s qualifications, work experience, education/training, key skills, market, collective bargaining agreements as applicable, and organizational considerations when extending an offer.
NewSenior Research Engineer Peraton IncSenior Research EngineerRed Bank, NJ$135,000–$216,000 / yearSuccess in this role demands genuine technical depth, sound product judgment about what will most increase the product's value to customers, and the communication skills to align a team that spans software engineers, domain experts, DoD stakeholders, and end users. Peraton is seeking a Senior Research Engineer to help drive an established program developing a mature, fielded RF spectrum planning, monitoring, and management system for Department of Defense customers.
Senior Research Director - Center for Responsible AI in Learning and Assessment Educational Testing ServiceSenior Research Director - Center for Responsible AI in Learning and AssessmentPrinceton, NJRemote$235,000–$275,000 / yearli>A strong record of scholarly impact such as: publications in leading venues relevant to the role (AI/ML/NLP and/or measurement/education research), recognized contributions to the field (invited talks, editorial/service roles, awards, high-impact collaborations), and/or demonstrated leadership of influential research programs. This position is designed for a distinguished AI researcher who can shape the future of assessment by advancing and applying state-of-the-art approaches in artificial intelligence, machine learning, natural language processing, and/or generative AI to high-stakes educational and workforce measurement.
NewSenior Research Engineer PeratonSenior Research EngineerRed Bank, New Jersey$135,000–$216,000 / yearp style="margin-bottom:6pt">Success in this role demands genuine technical depth, sound product judgment about what will most increase the product’s value to customers, and the communication skills to align a team that spans software engineers, domain experts, DoD stakeholders, and end users. Responsibilities: Peraton is seeking a Senior Research Engineer to help drive an established program developing a mature, fielded RF spectrum planning, monitoring, and management system for Department of Defense customers.
Senior Research Software Engineer Princeton UniversitySenior Research Software EngineerPrinceton, NJ$146,000–$160,000 / yearIdentify solutions for each project, establish a set of applicable best practices for individual or team use that is uniquely appropriate for that project (e.g version control, continuous integration and continuous delivery, software design, programming model, etc.), and enable long term maintainability and sustainability by documenting the projects in a descriptive and appropriately detailed manner. Has a strong command of the research domain with proficient understanding of the underlying science, math, statistics, data analysis, and algorithms of computational research questions at a level sufficient to converse on projects with Princeton's world-class researchers to consistently contribute to the ongoing work.
Senior Research Specialist I Princeton UniversitySenior Research Specialist IPrinceton, NJ$60,000–$75,000 / yearEssential qualifications:- Experience in a molecular biology lab environment- Experience breeding insects- Experience with CRISPR/Cas9 technology- Good communication skills- Excellent organizational skills and a strong attention to detail- Ability to lead a project independently and problem solve as needed- Ability to work well with others in a team environment- Ability to multi-task and prioritize in an environment with multiple demands and ongoing projects. Primary responsibilities will include assisting and leading research projects involving the development of genetic tools using CRISPR/Cas9 approaches, conducting and analyses animal behavioral experiments, and preparing high-throughput sequencing libraries etc.
Senior Director, Research-Skills Center Educational Testing ServiceSenior Director, Research-Skills CenterPrinceton, NJp>The Senior Director serves as the founding leader of the Skills Center and is accountable for setting the scientific vision, building organizational capacity, and securing external funding to advance ETS's leadership in the research and assessment of complex and durable skills across education and workforce contexts. Minimum of 10 years of progressively responsible experience in research leadership roles, including experience leading large-scale research programs, centers, or comparable research enterprises.
Senior Director, Research-Skills Center ETSSenior Director, Research-Skills CenterPrinceton, NJThe Senior Director serves as the founding leader of the Skills Center and is accountable for setting the scientific vision, building organizational capacity, and securing external funding to advance ETSs leadership in the research and assessment of complex and durable skills across education and workforce contexts. Minimum of 10 years of progressively responsible experience in research leadership roles, including experience leading large-scale research programs, centers, or comparable research enterprises.
Clinical Research Nurse - Oncology Research Department - Full Time Day RWJ Barnabas Health Medical IncClinical Research Nurse - Oncology Research Department - Full Time DayToms River, NJ$102,848.08–$135,702.50 / yearOpened in 1961, CMC has evolved into the states newest teaching hospital with four residency programs and Ocean Countys largest and most active health care facilitycaring for over 21,500 inpatients, 178,000 outpatients and 73,700 emergency department patients each year. Coordinate, evaluate and follow patient participation in clinical trials, This includes, but is not limited to identifying, enrolling and consenting patients, organizing study visits and follow-ups, responding to patient telephone calls and other related matters.
Clinical Research Nurse Hackensack University Medical CenterClinical Research NurseNJA day in the life of a Clinical Research Nurse at Hackensack Meridian Health includes: Assists the principal investigator in the preparation of proposed clinical trials by reviewing trial protocol, contacting each department who will provide resources during study and ensuring appropriate departments are notified and given a copy of proposed trial, scientific merit and accrual potential. The Clinical Research Nurse is responsible for coordinating and overseeing clinical research operations for all assigned clinical trials and participates in assessing, planning, implementing and evaluating Compliant Patient Care in clinical research trials.
Clinical Research Coordinator - Toms River, NJ RWJ Barnabas Health Medical IncClinical Research Coordinator - Toms River, NJToms River, NJ$22–$35 / hourp>Responsibilities will include, but are not limited to: implementing and overseeing group psychotherapy, working with clinical staff members to facilitate the psychotherapy groups, recruiting patients for relevant research studies, and serving as a liaison between unit staff and the Kleiman Lab Research team. The Barnabas Health Behavioral Health Center with Monmouth Medical Center Southern Campus Behavioral Health Services constitutes a freestanding 100-bed acute care psychiatric facility which provides inpatient and intensive outpatient programs for adults and older adults diagnosed with psychiatric and dual disorders.
Clinical Research - Flow Cytometrist 1 Syneos HealthClinical Research - Flow Cytometrist 1New JerseyWe are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
Associate Research Scientist RD PartnersAssociate Research ScientistLawrenceville, New Jersey£65,977–£82,472Experimental techniques could include, but are not limited to, the following: Processing human tissue and blood, Cell-based assays, Flow cytometry, ELISAs/MSD assays, RNA extraction and cDNA synthesis, Gene expression array cards. The qualified candidate will process human samples, maintain the laboratory's biobank (including sample storage and retrieval), and perform a range of experimental procedures under the guidance of senior scientists.
NewSenior Director Quant Pharm Penfield Search PartnersSenior Director Quant PharmPrinceton, NJThe Quantitative Pharmacology group is responsible for the oversight over drug development aspects related to clinical pharmacology and pharmacometrics of clinical development candidates, working in close collaboration with nonclinical and clinical functional areas. Development and execution of model-based analyses including translational PK/PD approaches, population pharmacokinetic models, exposure-response models, clinical trial design simulations, and quantitative systems pharmacology (QSP) modeling.
Senior Director, Mavacamten Medical Product Lead Bristol-Myers Squibb CoSenior 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.
Senior Software Engineer IQVIA Holdings IncSenior Software EngineerRed Bank, NJ$92,600–$231,600 / yearKey Responsibilities: • Design, develop, and maintain scalable web applications and services • Lead architectural decisions and technical planning across the stack • Build and enhance user interfaces using React • Develop backend services and APIs using Python or Go • Design and optimize relational database schemas using PostgreSQL • Leverage AWS infrastructure and services to ensure scalability, security, and performance • Collaborate with cross-functional teams in agile development processes • Mentor junior engineers and contribute to a culture of technical excellence • Own features end-to-end, from ideation to deployment and monitoring Requirements: • Education and Experience: o 5+ years of professional software development experience. • Technical Expertise: o Strong experience building user interfaces with React o Proficiency in Python or Go for backend development (ideally both) o Hands-on experience with AWS services (e.g., ECS, Lambda, S3, RDS, API Gateway) o Solid understanding of relational databases, especially PostgreSQL o Experience with Agile/Scrum methodologies.
Research Nurse CentraState Healthcare SystemResearch NurseFreehold, New Jersey$48–$81.60 / hourBeyond offering a wide range of advanced diagnostic and treatment options, CentraState is committed to being a valuable health partner, focusing on disease prevention, promoting healthy behaviors, and helping individuals of all ages live well. Demonstrates appropriate sample management activities to ensure the integrity of all biological samples; Manages or oversees the inventory of equipment and supplies related to the study and orders more as needed.
Senior Manager, Clinical Programming Genmab ASSenior Manager, Clinical ProgrammingPrinceton, NJFor 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. Please note that if you are applying for a position in the Netherlands, Genmab's policy for all permanently budgeted hires in NL is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the fixed-term employment contract.
Senior Director, Global Medical Oncology, Pumitamig GI/GU Cancers Bristol Myers SquibbSenior Director, Global Medical Oncology, Pumitamig GI/GU CancersPrinceton, NJ$229,380–$277,956 / yearThe role supports the development and implementation of the Global/US Pumitamig Medical Plan, leads or collaborates within Alliance Medical and cross-functional forums which includes the development of Integrated Evidence Plans (IEPs), scientific narratives, publication plans, congress strategies, field medical trainings, and external engagements. 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.
Senior Manager, Business Analyst, GDO - Site Engagement Bristol-Myers Squibb CoSenior Manager, Business Analyst, GDO - Site EngagementPrinceton, NJ$135,320–$163,976 / yearp>The Senior Manager, Business Analyst role contributes to the delivery of technology products and services within the Patient & Site Engagement domain, with a focus on enabling patient‑first, site‑centric capabilities that improve clinical trial feasibility, forecasting, and enrollment outcomes. This is a hands‑on role where the successful candidate partners closely with Product team and collaborates with business leaders, software engineers, project managers, IT teams, and external vendors to deliver and scale AI‑enabled digital solutions.
Senior Director, Global Medical Oncology, Pumitamig Breast Cancer and Other Rare Tumors Bristol Myers SquibbSenior Director, Global Medical Oncology, Pumitamig Breast Cancer and Other Rare TumorsPrinceton, NJ$229,380–$277,956 / yearThe role supports the development and implementation of the Global/US Pumitamig Medical Plan, leads or collaborates within Alliance Medical and cross-functional forums which includes the development of Integrated Evidence Plans (IEPs), scientific narratives, publication plans, congress strategies, field medical trainings, and external engagements. In collaboration with Global Medical Evidence Generation Team and within the Alliance partnership, develops and executes the integrated evidence generation plan (IEP), including Medical Affairs Pumitamig breast cancer and other rare tumors trials, and evaluation of Pumitamig breast cancer and other rare tumors investigator-initiated or collaborative trials.
Clinical Research Coordinator II - Toms River, NJ Iterative Scopes IncClinical Research Coordinator II - Toms River, NJToms River, NJBy combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need. Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies.
NewResearch Assistant Cardiology Consultants of PhiladelphiaResearch AssistantYardley, PAPart timeli>Medical Assistant certification or previous experience as a Medical Assistant, Clinical Assistant, LPN or healthcare support professional, required. This role assists with study coordination, patient interactions, data collection, regulatory documentation, and research-related administrative duties.
Senior Director, Medical Strategy, PH Johnson and JohnsonSenior Director, Medical Strategy, PHTitusville, NJFull timeThe Senior Director, Medical Strategy will be an expert in medical strategy development and will lead the overall medical strategy team to develop a portfolio medical strategy of products under his/her supervision with a goal to address medical and scientific issues and to ensure the appropriate use of all relevant J&J Medical Affairs supported products. • Please use the following language: • 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.
Sr DevOps Engineer IQVIA Holdings IncSr DevOps EngineerRed Bank, NJIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
Senior Specialist, Patient & Site Engagement Products, GDO BI&T Bristol-Myers Squibb CoSenior Specialist, Patient & Site Engagement Products, GDO BI&TPrinceton, NJ$76,080–$92,185 / yearThis is a hands-on role where the successful candidate will work closely with Global Patient Recruitment, Study and Patient Experience teams to gather requirements, design prototypes, work with Product Manager to develop and support the technology solutions throughout its lifecycle. 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.
NewSenior Medical Writer Nucleus Global LtdSenior Medical WriterYardley, PADrawn together from several backgrounds including the pharmaceutical industry, research, marketing, medical and regulatory writing, sales, publishing, digital media and design, we have the experience and all-round ability to conceive and deliver the best quality medical communications programs. We consider compensation more than just a base salary - that's why we also offer an exceptional range of flexible benefits, personal support and tailored learning and development opportunities all designed to help you realize your full potential both in life and at work.
Sr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology Preferred Syneos HealthSr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology PreferredNew JerseyProvides strategic direction to cross-functional project teams with minimal oversight to ensure that clinical documents (eg, Investigators' Brochures [IBs], Clinical Study Reports [CSRs], and marketing authorization submission documents) accurately and consistently present key data-driven clinical messages in accordance with program goals and regulatory requirements. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology PreferredSyneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success.
Senior Manager, Field Medical Affairs-Neurology (mid-Atlantic states) Regeneron Pharmaceuticals IncSenior Manager, Field Medical Affairs-Neurology (mid-Atlantic states)Trenton, NJ$150,500–$245,500 / yearSupport clinical research activities throughout the life cycle (phase 1-4), as well as Investigator Initiated Studies, focusing on identification of pre-clinical, clinical and post-marketing study investigators/ experts and sites in alignment with Medical Affairs objectives. To be considered a Clinical/Science doctorate Degree required (MD, PharmD, PhD, DNP, DVM) along with a minimum of 3-5 years related work experience preferred (clinical, managed care, or industry experience) including experience as a Medical Science Liaison.
NewSenior Director, TMF Services TransPerfectSenior Director, TMF ServicesPrinceton, New JerseySummary: The Senior Director, TMF Services is a senior leadership role responsible for the end-to-end management and strategic direction of the TMF Services division, overseeing service delivery, operational growth, and the continuous expansion of service offerings. The Senior Director will lead the strategic growth, operational excellence, and delivery of LMK's Trial Master File (TMF) services while building strong relationships across LMK, TransPerfect, and its global client base.
Senior Director, External innovation, Neuroscience Bristol-Myers Squibb CoSenior Director, External innovation, NeuroscienceNJ$273,900–$331,907 / yearClinical Strategy & Asset Leadership: Owns and drives business development strategy across given asset indications, aligned to overall neuroscience strategy, working on Target Product Profile (TPP), and relevant disease area strategy with multiple cross functional colleagues. 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.
Senior Associate R&D Quality and Risk Management Acadia Pharmaceuticals IncSenior Associate R&D Quality and Risk ManagementPrinceton, NJ$32.21–$40.29 / hourp>Position Summary: This role will work closely with the other team members in Quality Risk & Compliance (QRC) to assist in assessment, reporting on compliance and improvement of processes, tools and systems for Acadia clinical trials'' execution in a Good Clinical Practices (GCP) regulated environment. 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.
Senior Director, Therapeutic Area Lead, Mood – US Medical Affairs, Neuroscience 6120-Janssen Scientific Affairs Legal EntitySenior Director, Therapeutic Area Lead, Mood – US Medical Affairs, NeuroscienceTitusville, New Jersey$193,000–$333,500 / yearThe Senior Director, Therapeutic Area Lead, Mood, US Medical Affairs, Neuroscience will be a senior strategic decision-maker, balancing scientific rigor, regulatory compliance, patient centricity, and Medical Affairs scientific leadership to generate robust plans for data generation, data dissemination, and critical prelaunch initiatives supporting future indications. Reporting to the Vice President of US Medical Affairs, this senior leader will be accountable for the execution and attainment of key medical objectives in compliant alignment with the business strategy and lead the team to deliver high-quality communications regarding the science and clinical applications of our products and/or the disease states to external stakeholders on a regional, national, and international level.
Senior Dir, In-Vivo & Non-Clinical Pharmacology Bristol-Myers Squibb CoSenior Dir, In-Vivo & Non-Clinical PharmacologyNJ$252,640–$306,137 / yearThis leader will partner deeply with Research leadership and the Pharmacology, DMPK, Toxicology, and Translational Science units to deliver the applications, workflow capabilities, AI, and supporting data flows that enable non-clinical decisions across in-vivo biology, DMPK, ADME, non-clinical safety, toxicology, and bioanalytical science. Non-clinical pharmacology generates the evidence that determines which candidates enter humans, and this role matters now because scientists need better integrated applications, AI, and workflows to generate, interpret, and act on that evidence with greater speed and confidence.
Senior Manager, Global Clinical Scientist (Cell Therapy) Bristol-Myers Squibb CoSenior Manager, Global Clinical Scientist (Cell Therapy)Princeton, NJ$173,390–$210,110 / 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.
Senior Manager, Global Clinical Scientist - Psychiatry Bristol-Myers Squibb CoSenior Manager, Global Clinical Scientist - PsychiatryPrinceton, NJ$173,390–$210,110 / yearp>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. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/.
Senior Manager, Global Clinical Science, Neuroscience Bristol-Myers Squibb CoSenior Manager, Global Clinical Science, NeuroscienceNJ$173,390–$210,110 / 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.
Senior Sales & Business Development Representative - Health Technology Sales (Ovid Synthesis Sales Specialist) Wolters Kluwer N.V.Senior Sales & Business Development Representative - Health Technology Sales (Ovid Synthesis Sales Specialist)Princeton, NJ$85,600–$149,400 / yearp>Within the Health Division of Wolters Kluwer, the Health Research business provides health solutions that help clinical professionals learn, practice and conduct research and advance their careers using market-leading tools and evidence-based information. This position will collaborate closely with colleagues from the Ovid Sales Team to establish new sales of Ovid Synthesis at existing accounts, while also working independently to create secure new deals.