NewSenior Accountant - Hybrid Kforce Inc.Senior Accountant - HybridPrinceton, NJ$100,000–$112,000Assist with the preparation of quarterly unaudited and annual audited financial statements of multiple construction projects in accordance with GAAP to comply with the reporting requirements of the lender and ownership agreements, which include tax equity and cash equity ownership structures. Summary: The Senior Accountant is responsible for financial data management, journal entries, account reconciliations, timely completion, and assistance with monthly and quarterly internal financial reporting, internal controls, and accounting for various components of the company.
NewSenior Accountant Kforce Inc.Senior AccountantPrinceton, NJ$90,000–$110,000Summary: Reporting to the Manager of Accounting, the Senior Accountant is responsible for assisting in preparing monthly and quarterly internal financial reporting, account reconciliations, internal controls, and accounting for various components of the company. Work with internal functional departments (e.g., Treasury, Asset Management, Engineering, and Procurement) and external groups to ensure reported financial results are completed in a timely and accurate manner in compliance with company policies and procedures.
NewSenior Tax Manager Kforce Inc.Senior Tax ManagerRed Bank, NJ$170,000–$210,000Employee pay is based on factors like relevant education, qualifications, certifications, experience, skills, seniority, location, performance, union contract and business needs. By clicking “Apply Today” you agree to receive calls, AI-generated calls, text messages or emails from Kforce and its affiliates, and service providers.
NewSenior Tax Associate Kforce Inc.Senior Tax AssociatePrinceton, NJ$100,000–$116,000They will be responsible for supporting the Senior Manager for all tax planning activities, including US federal and state income tax, transaction tax return support, cash tax optimization, credits and incentives, and transaction diligence. 3+ years of federal and state tax planning or compliance for partnerships with a public accounting firm or large corporate tax department; Experience with private equity or real estate tax is a plus.
NewSenior Tax Analyst - Partnerships Kforce Inc.Senior Tax Analyst - PartnershipsPriceton, NJ$100,000–$115,000Summary: The candidate will be responsible for supporting the Senior Manager for all tax planning activities, including US federal and state income tax, transaction tax return support, cash tax optimization, credits and incentives, and transaction diligence. 3+ years of federal and state tax compliance or planning for partnerships with a public accounting firm or large corporate tax department; Experience with private equity or real estate tax is a plus.
NewSr. Manager, Medical Review - Contract TalentBurst, Inc.Sr. Manager, Medical Review - ContractPlainsboro Township, NJRemote$38–$40 / hourOther notable details about the environment from the hiring manager about this role: Role works cross-functionally with multiple internal stakeholders/partners (i.e. regulatory review, legal, ethics, Medical affairs, commercial). • For designated therapeutic area of responsibility, attends, advises, and approves in review meetings as the lead Medical Reviewer for promotional review.
NewSenior Financial Reporting Consultant AtriumSenior Financial Reporting ConsultantWall, NJ$50–$52 / hourBy applying to this job, you agree to receive calls, AI-generated calls, text messages, and/or emails from Atrium and its affiliates, and contracted partners. Guided by our Applicant-Centric™ approach, we foster an environment of collaboration, high performance, and innovation where your talents are valued, and your achievements are celebrated.
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.
NewAVP, Senior Compliance Manager First Commerce BankAVP, Senior Compliance ManagerLakewood, NJSkill(s): Strong background in the design of compliance programs; in-depth knowledge of financial services and regulatory industry practices; regulatory, industry, and operational knowledge with respect to compliance monitoring and testing; working knowledge of applicable banking regulations; knowledge of compliance monitoring principles including planning, regulatory controls, operating effectiveness testing, and reporting; proficient in MS Office (Word/PowerPoint/Excel); excellent written and verbal communication skills; strong organizational, problem-solving, and analytical skills; ability to work effectively with others at all levels across the organization and provide authoritative guidance to management and staff. Serve as Subject Matter Expert (SME) for applicable lending and deposit regulations, including ECOA, TRID, TILA/RESPA, HMDA, RESPA, Regulation CC, Regulation DD, Expedited Funds Availability Act, Truth in Savings, FDIC Act, and Regulation E. Assist the Chief Compliance Officer in the oversight of the annual compliance monitoring program: develop the monitoring schedule based on the Compliance Risk Assessment, coordinate reviews with third-party consultants and internal managers, maintain all review reports and workpapers for examiner access, and follow up with management on corrective actions.
Senior Research Investigator, Clinical Pharmacology Bristol-Myers Squibb CoSenior Research Investigator, Clinical PharmacologyPrinceton, 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 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.
Sr. Clinical Research Associate Systimmune IncSr. 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. 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.
NewSr. Research Specialist II Princeton UniversitySr. Research Specialist IIPrinceton, New Jersey$80,000–$85,000 / yearFull timeIn this position, the scientist will contribute to several funded collaborative projects aimed at (1) developing novel cell type specific viral (AAV-based) tools in nonhuman primate models and (2) producing single cell genomic (RNA-seq and ATAC-seq) datasets to understand epigenetic and transcriptomic properties of brain cell types. Responsibilities: • Develop advanced experimental workflows for profiling the molecular contents and biological states of thousands of individual cells or nuclei in brain tissue; applying or developing technologies to profile brain cell types .
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.
Sr. Clinical Research Associate SystimmuneSr. Clinical Research AssociatePrinceton, NJFull timePrepare 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 Benefit Consultant JBM Planning and Consulting LLCSenior Benefit ConsultantBordentown, NJFull timeWith that growth comes a significant expansion of our service scope, our reporting cadence to the Fund Commissioners, and our role advising on plan design, vendor management, pharmacy cost containment, network performance, and stop-loss strategy. Reporting and PresentationPrepare the monthly Program Manager’s Report to the Fund Commissioners — drafting narrative, building exhibits, integrating pharmacy and network data, and maintaining the established report format.
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. Resumes sent to Acadia employees in the absence of an executed search agreement will not obligate Acadia in any way with respect to the future employment of those individuals or potential remuneration to any recruiter or search firm.
Senior Research Engineer PeratonSenior Research EngineerRed Bank, New Jersey$135,000–$216,000 / yearFull timeSuccess 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.
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.
NewSenior Research Software Engineer Princeton UniversitySenior Research Software EngineerPrinceton, NJIdentify 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 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 / yearA 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.
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.
Senior Director, Research-Skills Center Educational Testing ServiceSenior 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 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.
NewClinical Research Associate (CRA) – All levels (I/II/Senior) Theradex OncologyClinical Research Associate (CRA) – All levels (I/II/Senior)Princeton, New JerseyFull timeWe will assess the specific title and level of entry during the interview and assessment process since the actual salary offer will be based on a number of factors, including but not limited to the candidate’s qualifications, experience, skills, and competencies for the role. As a Clinical Research Associate with experience managing clinical trial sites, the number years and type of monitoring experience will determine CRA level.
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 - 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.
Senior 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.
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 Director, Quantitative Pharmacology Sun Pharmaceutical Industries LtdSenior Director, Quantitative PharmacologyPrinceton, NJ$215,500–$239,500 / yearThe 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.
Research Nurse CentraState Healthcare SystemResearch NurseFreehold, New Jersey$48–$81.60 / hourPart timeBeyond 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 Health Services Researcher- Remote Community Health Center IncSenior Health Services Researcher- RemoteNJRemoteThe system delivers primary care to more than 150,000 patients in Connecticut, and extends access to specialty care for more than 2.5 million individuals across the U.S. It is a national accrediting body for organizations training advanced practice providers, and offers accredited education and training for Medical Assistants in multiple states. As an incubator for new ideas in areas including social justice, the environment, and social determinants of health, the MWHS is addressing challenges faced by providers caring for underserved communities, creating innovative and impactful initiatives led by nationally and internationally recognized experts.
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.
Sr DevOps Engineer,IQVIA Digital IQVIASr DevOps Engineer,IQVIA DigitalRed Bank, New JerseyIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time).
Senior 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.
Research Assistant Cardiology Consultants of PhiladelphiaResearch AssistantYardley, PAPart timeMedical 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, 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.
***REVISED***** Postdoctoral Research Associate Princeton University***REVISED***** Postdoctoral Research AssociatePrinceton, NJI understand Princeton University expects all applicants to exhibit the highest level of integrity and ethical conduct, and that my concealment of any information, or my provision of misleading or false information, the University considers to be relevant will constitute grounds for it to cease the consideration of my employment or, if I am selected or hired, to withdraw or rescind my job offer or to terminate my employment, as applicable. Applications must be submitted online at https://www.princeton.edu/acad-positions/position/39502, and should include a cover letter, curriculum vitae that includes a list of publications, a brief statement (3 pages max) of research interests and goals and the names and contact information for three references.
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.
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.
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 / yearThe 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, 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 Manager, Clinical Scientist Gan & Lee PharmaceuticalsSenior Manager, Clinical ScientistNJFull timeExperiences in metabolic diseases (Diabetes, Obesity, NASH, NAFLD, etc.), Endocrinology (CKD, CRF, etc.), and Nutrition and Weight Management related drug development are a plus. The position will work with Gan & Lee clinical program lead(s) to provide the scientific and clinical leadership and inputs in meeting the development objectives for the program.
Sr. Manager, Medical Review TalentBurst, Inc.Sr. Manager, Medical ReviewPlainsboro Township, NJRemote$38–$40 / hourOther notable details about the environment from the hiring manager about this role: Role works cross-functionally with multiple internal stakeholders/partners (i.e. regulatory review, legal, ethics, Medical affairs, commercial). • For designated therapeutic area of responsibility, attends, advises, and approves in review meetings as the lead Medical Reviewer for promotional review.
NewSenior Director, Educational Strategy The Wyanoke GroupSenior Director, Educational StrategyNew JerseyRemoteSenior Director, Educational Strategy Job Summary:Build and maintain relationships with commercial supporters to ensure strong communication of Vindico capabilities, experience, thinking, and successes. Providing oversight and supporter communication for funded CME activities, and established relationships with grant management and medical affairs teams at pharmaceutical, biotechnology, and medical device companies.