Daiichi Sankyo, Inc.Senior Director, Clinical Safety Scientist Daiichi Sankyo, Inc.Senior Director, Clinical Safety ScientistBasking Ridge, NJ$242,700ā$404,500 / yearFull timeLead scientist team to collaborate with safety physicians, regulatory affairs, clinical development, other functions and external partners to deliver high-quality safety assessments, regulatory submissions, aggregate reports, and responses to health authority queries. In addition to operational oversight, this role contributes to the development of global safety processes, talent capability building, and strategic alignment across the broader Clinical Safety and Pharmacovigilance (CSPV) function and the enterprise.
JoulĆ©NewFood Scientist I JoulĆ©Food Scientist ITinton Falls, NJ$65,000ā$70,000 / yearBring key skills and knowledge in generating new product ideas, processing concepts from idea to final production startup, and spearheading new technology development for extruded and injection-molded products. System One, and its subsidiaries including JoulĆ© and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America.
Vaco LLCData Scientist - Sr. Associate Vaco LLCData Scientist - Sr. AssociateNew York, NY$130,000ā$175,000Determining compensation for this role (and others) at Vaco by Highspring depends upon a wide array of factors including but not limited to: the individualās skill sets, experience and training; licensure and certification requirements; office location and other geographic considerations; other business and organizational needs. Determining compensation for this role (and others) at Vaco/Highspring depends upon a wide array of factors including but not limited to the individualās skill sets, experience and training, licensure and certifications, office location and other geographic considerations, as well as other business and organizational needs.
Daiichi Sankyo, Inc.Senior Director, Clinical Safety MD Daiichi Sankyo, Inc.Senior Director, Clinical Safety MDBasking Ridge, NJ$280,350ā$467,250 / yearFull timeThe individual assuming this role may function as a key member of the Global Product Team in collaboration with Clinical Development, Regulatory, Project Management, Biostatistics, Pharmacology, and other departments to strategically manage benefit-risk throughout the lifecycle of the drug. Depending on the status of development of the compound, lead and medical-scientifically direct a team of physicians and scientists responsible for a compound/product including project-specific training and coaching of team members and review of team output cross-functionally.
Aquestive Therapeutics Inc.Senior Formulation Scientist Aquestive Therapeutics Inc.Senior Formulation ScientistWarren, NJFinal determinations with respect to salary will take into account a number of factors, which may include, but not be limited to the primary work location and the chosen candidateās relevant skills, experience, and education. Designs and optimizes formulations to achieve drug product properties for controlled delivery of drugs (i.e. oral, transmucosal, and topical) .
MindlanceMedical Laboratory Scientist MindlanceMedical Laboratory ScientistClifton, NJ$30ā$40 / hourMinimum of 1 year of clinical laboratory experience in highly complex testing for those with BS/BA in Chemistry or Biology. Performs simple routines, such as preparing solutions and sterilizing equipment for testing.
Merck & Co IncSr. Scientist, Clinical Operations Merck & Co IncSr. Scientist, Clinical OperationsRahway, NJ$117,000ā$184,200 / yearOther responsibilities include: Collaborating cross-functionally in the development of Protocol and related study materials (e.g., ICF documents/amendments); Partners with the Study Manager on study deliverables. Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities.
Biogen IncClinical Scientist, Immunology Biogen IncClinical Scientist, ImmunologyNY$206,000ā$283,000 / yearRegular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance. As a vital contributor, you will play a critical role in advancing programs from translational insights through early-phase clinical studies, ensuring strong alignment between mechanisms, biomarkers, and clinical strategy across immune-mediated diseases, including organ transplantation.
Regeneron Pharmaceuticals IncAssociate Director, Clinical Scientist, Genetics Medicine Regeneron Pharmaceuticals IncAssociate Director, Clinical Scientist, Genetics MedicineTarrytown, NY$176,100ā$287,300 / yearAuthors and/or reviews documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports with minimal guidance and supports the development of regulatory documents; performs quality review and may approve; adjudicate and resolve cross functional comments with minimal support. This role may be for you if: Ability to lead activities within a matrix environment; Exhibits confidence and professional diplomacy, while effectively relating to people at all levels internally and externally; Demonstrated ability to Influence within team and may influence across functionally.
Regeneron Pharmaceuticals IncManager, Internal Medicine, Clinical Scientist (Immune/Inflammatory) Regeneron Pharmaceuticals IncManager, Internal Medicine, Clinical Scientist (Immune/Inflammatory)Tarrytown, NY$128,600ā$210,000 / yearAs a Manager within Clinical Sciences, a typical day may include the following: Member of the Clinical Study Team and the Global Clinical SubTeam; regularly attends and actively participates in study team meetings. The Manager reports to the Associate Director/Director Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.
Merck & Co IncSenior Principal Scientist, Clinical Research, Immunology Merck & Co IncSenior Principal Scientist, Clinical Research, ImmunologyRahway, NJ$282,200ā$444,200 / yearWork closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and assist the Executive Director in ensuring that appropriate corporate personnel are informed of the progress of studies of our company and competitors' drugs and internal and external expert opinion on scientific questions relevant to his/her areas of responsibility. Required Skills: Clinical Development, Clinical Medicine, Clinical Research Management, Clinical Studies, Clinical Trial Development, Clinical Trials, Dermatology, Drug Development, Gastroenterology, Inflammatory Bowel Diseases, Pharmaceutical Industry, Regulatory Compliance, Rheumatology.
Merck & Co IncScientist, Clinical Operations Merck & Co IncScientist, Clinical OperationsRahway, NJ$96,200ā$151,400 / yearJob Responsibilities: Responsible for specific clinical/scientific activities on a single study or across multiple studies (e.g., medical monitoring, lab specimen tracking/reconciliation, adjudication support, preparation of meeting materials). Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities.
Regeneron Pharmaceuticals IncSenior Manager, Internal Medicine, Clinical Scientist (Immune/Inflammatory) Regeneron Pharmaceuticals IncSenior Manager, Internal Medicine, Clinical Scientist (Immune/Inflammatory)Tarrytown, NY$150,500ā$245,500 / yearThis role may be for you if: ā¢ Demonstrated ability to influence within team and may influence cross functionally ā¢ Exhibit strong analytical and influencing skills; ability to communicate concise and clear messages, strong presentation skills ā¢ Independently uses professional concepts and company objectives to resolve complex issues in creative and effective ways ā¢ Strong management, interpersonal and problem-solving skills ā¢ Proven knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & medical writing skills ā¢ Knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines ā¢ Proven track in clinical trial process improvements ā¢ Considerable organizational awareness, including significant experience working cross-functionally. As a Senior Manager in Clinical Sciences, a typical day may include the following: ā¢ Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; ā¢ Participates in collaborative activities with other departments; ā¢ Member of the Clinical Study Team and Global Clinical SubTeam.
Regeneron Pharmaceuticals IncSenior Manager, Internal Medicine, Clinical Scientist (Ophthalmology) Regeneron Pharmaceuticals IncSenior Manager, Internal Medicine, Clinical Scientist (Ophthalmology)Tarrytown, NY$150,500ā$245,500 / yearThis role may be for you if: ā¢ Demonstrated ability to influence within team and may influence cross functionally ā¢ Exhibit strong analytical and influencing skills; ability to communicate concise and clear messages, strong presentation skills ā¢ Independently uses professional concepts and company objectives to resolve complex issues in creative and effective ways ā¢ Strong management, interpersonal and problem-solving skills ā¢ Proven knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & medical writing skills ā¢ Knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines ā¢ Proven track in clinical trial process improvements ā¢ Considerable organizational awareness, including significant experience working cross-functionally. Applies basic scientific expertise to support initiation and execution of clinical research and development studies for early and/or late stage assets; Assists with development of the Expanded Synopsis and may author clinically relevant sections and review other scientific portions of clinical trial protocols and amendments.
Merck & Co IncClinical Director (Principal Scientist), Clinical Research, Immunology - Rheumatology Merck & Co IncClinical Director (Principal Scientist), Clinical Research, Immunology - RheumatologyRahway, NJ$255,800ā$402,700 / yearThe Clinical Director is responsible for maintaining a strong scientific fund of knowledge by: Maintaining awareness of scientific developments within their area of expertise, in terms of new scientific findings, research methodologies. Job Description: The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Immunology therapeutic area.
Regeneron Pharmaceuticals IncSenior Manager, Clinical Scientist, Genetics Medicine Regeneron Pharmaceuticals IncSenior Manager, Clinical Scientist, Genetics MedicineTarrytown, NY$150,500ā$245,500 / yearAs a Senior Manager, a typical day may include the following: Supports the cross-functional study team on the following activities, including but not limited to: Contributes to the writing of sections of Clinical Study Concepts (CSCs) and Clinical Study Protocols (CSPs) and amendments. Drafts portions of the clinical sections in regulatory and clinical documents such as: regulatory agency briefing books, IND/IMPD submissions, investigator's brochure, informed consent forms, IRB/IEC submissions, clinical study reports, abstracts/manuscripts for publication, etc.
CVS Health CorpLead Data Scientist - Clinical Informatics (Clinical Data Standards) CVS Health CorpLead Data Scientist - Clinical Informatics (Clinical Data Standards)NY$130,295ā$260,590 / yearA&BC leverages advanced analytics, clinical informatics, and hypothesis-driven approaches to transform data into actionable, customer-centric insights that drive growth, improve health outcomes, and expand access to healthcare across all CVS Health businesses. Enable self-service analytics by building well-documented, validated, and reusable data assets (tables, views, features) that empower analysts and data scientists to work independently with clinical data.
Legend Biotech CorpSenior Clinical Research Scientist Legend Biotech CorpSenior Clinical Research ScientistSomerset, NJ$127,313ā$167,099 / yearHeadquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. Contribute to the planning and execution of external meetings and internal stakeholder meetings (e.g., Ad Boards, IMs, Governance, DMCs, Regulatory Authority, Dose Escalation meeting); responds to or triages questions for appropriate escalations.
TEEMA GroupClinical Lab Scientist TEEMA GroupClinical Lab ScientistWhite Plains, NY$63,386ā$120,685Histotechnicians will utilize both manual and automated techniques to produce high-quality pathology slides, while Clinical Lab Scientists will oversee the accuracy and quality of results across all phases of testing. For Histotechnician Candidates: * NYS Clinical Laboratory Technician License or NYS Histotechnician License.
KingdomScientist, Clinical Development KingdomScientist, Clinical DevelopmentBrooklyn, New YorkIn this role, you'll report to the Senior Scientific Director, and will work with our science team, co-founders, CRO partners, and the commercial team to: Run Kingdom's pet clinical study program end-to-end: Ownership and autonomy: End-to-end control of an established pet clinical program (9+ completed studies, several peer-reviewed publications) and substantial latitude to shape our clinical AI infrastructure.
Regeneron Pharmaceuticals IncManager, Clinical Scientist, Hematology Regeneron Pharmaceuticals IncManager, Clinical Scientist, HematologyTarrytown, NY$128,600ā$210,000 / yearAssists with and may authors/review documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports and may support development of regulatory documents; may perform quality review. The Manager reports to either Associate Director or Director, Clinical Sciences and collaborates closely with Medical Director (MD) to provide scientific expertise necessary to design and deliver on clinical studies and programs.
Merck & Co IncSenior Principal Scientist (Senior Director), Clinical Research, ADC Merck & Co IncSenior Principal Scientist (Senior Director), Clinical Research, ADCRahway, NJ$282,200ā$444,200 / yearThe Senior Director is responsible for maintaining a strong scientific fund of knowledge by: Maintaining awareness of scientific developments within his/her area of expertise, in terms of new scientific findings, research methodologies. The Senior Clinical Director (Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new medicines in the Oncology Asset therapeutic area.
R37 Lab, R1 RCMApplied AI Scientist, Clinical AI Agents R37 Lab, R1 RCMApplied AI Scientist, Clinical AI AgentsNew York, New YorkPhare Health is now part of R1 and its AI innovation engine, R37 Lab, bringing Phareās frontier clinical reasoning technology together with one of the largest healthcare platforms in the U.S. At R37 and Phare, we are building the first AI-native Healthcare Revenue Operating System: a connected platform that reasons over full medical records, payer logic, and financial workflows to automate medical coding, billing, and follow-up. You will be embedded in hard healthcare problems ā clinical documentation integrity, medical coding, denial prevention, appeals, revenue cycle workflows, and payer logic ā and will own the loop from problem framing to agent design, evaluation, deployment, trace analysis, and ongoing improvement.
N-Power Medicine IncClinical Data Scientist N-Power Medicine IncClinical Data ScientistNY$132,000ā$226,000 / yearN-Power Medicine is seeking a Clinical Data Scientist to own the final stage of its clinical data pipeline, transforming complex datasets from manual abstraction, AI models, and electronic sources into high-quality, analysis-ready deliverables for pharmaceutical partners. This role sits at the intersection of data science and clinical research, requiring expertise in data cleaning, transformation, and statistical programming (R, Python, SQL) to generate reports and ensure data integrity, accuracy, and regulatory compliance.
White Plains HospitalClinical Laboratory Scientist/Histotechnician White Plains HospitalClinical Laboratory Scientist/HistotechnicianWHITE PLAINS, NY$93,873ā$120,685.50 / yearPrimary Population Served Check appropriate box(s) below: Neonatal (birth 28 days) Patients with exceptional communication needs Infant (29 days less than 1 year) Patients with developmental delays Pediatric (1 12 years) Patients at end of life Adolescent (13 17 years) Patients under isolation precautions Adult (18 64 years) Patients with cultural needs Geriatric ( 65 years) Ć¢'All populations Bariatric Patients with weight related comorbidities Non-patient care population The responsibilities and tasks outlined in this job description are not exhaustive and may change as determined by the needs of White Plains Hospital. Any hazardous chemicals the employee may be exposed to are listed in the hospitals SDS (Safety Data Sheet) data base and may be accessed through the hospitals Intranet site (Employee Tools/SDS Access).
St. Clare's - DoverNewClinical Laboratory Scientist St. Clare's - DoverClinical Laboratory ScientistDover, New JerseyEach individual performing the above procedures must: 1) adhere to the laboratory's procedures for the collection, processing, analysis, and reporting of patient test results, 2) follow the laboratory's established quality control policies and procedures in documenting all corrective actions taken when test systems deviate from the laboratory's established performance specifications, 3) be capable of identifying problems that may adversely affect test performance and either correct the problem or immediately notify your immediate supervisor, Director, or Medical Director, 4) perform a wide variety of laboratory procedures requiring independent judgment using both manual and automated methods in Hematology, Blood Bank, Chemistry, Urinalysis, Coagulation, Microbiology, Immunology, and any other discipline as introduced into the laboratory, 5) perform and document maintenance - daily, weekly, monthly, or as needed on instruments and equipment as appropriate, 6) review the accuracy of patient results prior to releasing or reporting, 7) recognize age specific differences in expected results for newborns to geriatrics, 8) ensure that the testing of proficiency testing samples are tested in the same manner as patient samples and that collaboration with other laboratories is prohibited prior to the reporting of proficiency testing results to the appropriate agencies, 9) may be required to perform venipuncture or capillary puncture on various age groups from newborn to geriatrics, 10) assist in the development and maintenance of laboratory policies and procedures, 11) adheres to all department and hospital policies and procedures related to safety, infection control, emergency preparedness, and human resources, 12) 12) in the absence of a supervisor, may be assigned/identified as Lead Tech, having responsibility for the section or department during their shift, 13) may be assigned responsibilities related to LIS and/or POCT. Saint Clare's Health includes CMS 5-Star Rated hospitals and is an award-winning provider of safe, high quality, compassionate care, serving the communities of Morris, Warren and Sussex counties.
Latitude Health IncStaff Data Scientist, Clinical Performance Latitude Health IncStaff Data Scientist, Clinical PerformanceNew York City, NY$160,000ā$200,000 / yearWhile your primary focus is evaluative, you will be a key player in the broader clinical DS ecosystem, collaborating on patient risk stratification and building the forecasting engines that predict our quality performance across various value-based care programs. Automate Model Lifecycles with AI Agents: Architect and oversee AI-driven agents that autonomously manage the end-to-end lifecycle of our statistical models - leveraging automation for continuous training, deployment, performance monitoring, and proactive model refreshes.
PhilipsScientist, Advanced Clinical Innovation Partnerships (ACIP), IGTS, West PhilipsScientist, Advanced Clinical Innovation Partnerships (ACIP), IGTS, WestNY$122,906ā$196,650 / yearYour Skills Include: Working knowledge and practical experience with AI-enabled solutions and data-driven innovation in clinical or research settings; Strong interpersonal, communication, and stakeholder management skills, with the ability to effectively engage with physician investigators, clinical researchers, hospital administrators, R&D, product and marketing teams, and commercial stakeholders. Design, coordinate, execute, and or support scientific research and validation programs, including concept studies, feasibility work, and collaborative research or sponsor-supported studies, using rigorous protocols to demonstrate scientific merit, clinical impact, and workflow value in line with Clinical Development Strategy.
NovartisPrincipal Clinical Data Scientist NovartisPrincipal Clinical Data ScientistEast HanoverWorking at the heart of cross-functional clinical trial teams, you will collaborate closely with data quality experts, clinical teams, and external partners, fostering a high-performing, well-organized team environment. You will lead end-to-end data management activities, overseeing study delivery, driving key performance indicators, and ensuring inspection-ready data that supports timely submissions to health authorities.
MRINetwork JobsClinical Laboratory Scientist - Microbiologist MRINetwork JobsClinical Laboratory Scientist - MicrobiologistPleasantville, New YorkIdentifying and documenting problems that may adversely affect test performance and notifying the supervisor, assistant director or director and documenting all corrective actions taken when test systems deviate from the laboratoryās established performance specifications. Any hazardous chemicals the employee may be exposed to are listed in the hospitalās SDS (Safety Data Sheet) data base and may be accessed through the hospitalās Intranet site (Employee Tools/SDS Access).
MRINetwork JobsClinical Laboratory Scientist-Hematologist MRINetwork JobsClinical Laboratory Scientist-HematologistWhite Plains, New YorkIdentifying and documenting problems that may adversely affect test performance and notifying the supervisor, assistant director or director and documenting all corrective actions taken when test systems deviate from the laboratoryās established performance specifications. Any hazardous chemicals the employee may be exposed to are listed in the hospitalās SDS (Safety Data Sheet) data base and may be accessed through the hospitalās Intranet site (Employee Tools/SDS Access).
Regeneron Pharmaceuticals IncPrincipal Scientist, Precision Medicine Strategy Lead (Clinical Biomarkers) Regeneron Pharmaceuticals IncPrincipal Scientist, Precision Medicine Strategy Lead (Clinical Biomarkers)Tarrytown, NY$128,600ā$210,000 / yearWe are seeking a Precision Medicine Strategy Lead (PMSL) at the Principal Scientist level responsible for the clinical biomarker strategy for multiple clinical stage assets in Regeneron's Immunology & Inflammation (I&I), Ophthalmology and Infectious Diseases portfolios. They will thrive in a collaborative environment and regularly partner with research teams, clinical development, laboratory operations, companion diagnostics, clinical operations, tech centers, alliance partners, external academic collaborators, and others.
PhamilyNewLead Data Scientist, Causal Inference & Clinical Outcomes Contractor (Remote) PhamilyLead Data Scientist, Causal Inference & Clinical Outcomes Contractor (Remote)New York City, New YorkRemotePhamily, the company's core technology platform, has transformed chronic disease management with clinically tested AI and easy-to-use technology that enables physicians and care teams to offer high-touch, individualized patient care that has been proven to reduce investment in extra labor and the overall cost of care. In this 16-week engagement starting May 7, 2026, you will lead a rigorous clinical outcomes study for our key client, Silver Cross Medical Group (SCMG), to quantify the impact of our Advanced Primary Care Management (APCM) and Chronic Care Management (CCM) programs.
Regeneron Pharmaceuticals IncAssociate Director, Clinical Scientist, Internal Medicine (Cardio, Metabolic, & Renal) Regeneron Pharmaceuticals IncAssociate Director, Clinical Scientist, Internal Medicine (Cardio, Metabolic, & Renal)Tarrytown, NY$176,100ā$287,300 / yearAs an Associate Director, a typical day may include the following: ā¢ May function as lead Clinical Scientist for program, and/or as delegate of Therapeutic area Lead Clinical Scientist; ā¢ Member of the Clinical Study Team and Global Clinical SubTeam; ā¢ Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; ā¢ May represent function in collaborative activities with other departments. Directly or indirectly contributes to the development of innovations; ā¢ Identifies opportunities for process improvements; ā¢ Resolves novel problems requiring creative application of advanced skill, training, and education; ā¢ Demonstrated leadership and accomplishment in all aspects of conducting global clinical trials and execution of clinical programs.
Regeneron Pharmaceuticals IncSenior Scientist - Clinical Bioanalysis Regeneron Pharmaceuticals IncSenior Scientist - Clinical BioanalysisTarrytown, NY$109,900ā$179,300 / yearResponsible for the oversight of all study-related activities, including protocol review, approval of the bioanalytical data, assessing the impact of any incurred deviations, accurate reporting of data in reports and submitting documentation for archival, as appropriate. Ensures compliance, as appropriate, for all laboratory work and documentation in accordance with working practices, company SOPs, bioanalytical method procedures (BMPs), and regulations (e.g., GLP and GCP).
Pfizer IncDirector, Clinical Development Scientist (Non-MD) Pfizer IncDirector, Clinical Development Scientist (Non-MD)New York City, NY$176,600ā$294,300 / yearProvides clinical guidance to the development of the clinical data collection strategy, instruments, and data review plan, ensuring alignment with the protocol and SAP, optimized data collection principles, and clinical data review best practice; sets the clinical data review strategy and leads the team in the review of emerging clinical data and trends; reviews and queries data; presents data to internal and external stakeholders; partners with site-facing colleagues in support of data issue resolution; ensures all clinical queries are appropriately addressed in support of database lock. Provides clinical guidance to the development of the Safety Review Plan and Safety Narrative Plan; reviews safety data and ensures clinical documents are updated in response to emerging safety profile; tracks and reconciles Serious Adverse Events; leads clinical safety data discussion during Safety Review Team meetings in collaboration with Medically Qualified Individual(s); reviews safety narratives.
Pfizer IncClinical Development Scientist (Senior Director) Pfizer IncClinical Development Scientist (Senior Director)New York City, NY$214,900ā$358,100 / yearProvides clinical guidance to the development of the clinical data collection strategy, instruments, and data review plan, ensuring alignment with the protocol and SAP, optimized data collection principles, and clinical data review best practice; sets the clinical data review strategy and leads the team in the review of emerging clinical data and trends; reviews and queries data; presents data to internal and external stakeholders; partners with site-facing colleagues in support of data issue resolution; ensures all clinical queries are appropriately addressed in support of database lock. Provides clinical guidance to the development of the Safety Review Plan and Safety Narrative Plan; reviews safety data and ensures clinical documents are updated in response to emerging safety profile; tracks and reconciles Serious Adverse Events; leads clinical safety data discussion during Safety Review Team meetings in collaboration with Medically Qualified Individual(s); reviews safety narratives.
Tanabe Pharma America IncClinical Research Scientist Tanabe Pharma America IncClinical Research Scientistjersey city, NJReporting to the Senior Director, Clinical Development, the Clinical Research Scientist will provideleadership in the direction, planning, execution, and interpretation of clinical protocols, research, data collection activities, and clinical operations. Oversee and coordinate the collection of and/or collect pre-study documents Participate in data review and discrepancy resolution, team meetings/presentations with increasinglevels of independence and support the Program Clinical Leader or Sr.
Legend Biotech CorpPrincipal Scientist, Clinical Biomarker, Immunology, Immuno-Oncology, & Hematology Contractor Legend Biotech CorpPrincipal Scientist, Clinical Biomarker, Immunology, Immuno-Oncology, & Hematology ContractorSomerset, NJHeadquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. Leverage advanced single-cell technologies (e.g., scRNA-seq) to deeply profile immune cell compartments, particularly T-cell states and exhaustion markers, to inform patient stratification and biomarker hypotheses.
John Wiley & Sons IncPrincipal Scientist, Clinical Outcomes John Wiley & Sons IncPrincipal Scientist, Clinical OutcomesHoboken, NJ5+ years working with Clinical Outcome Assessments in a scientific, regulatory, or commercial context, including roles in pharmaceutical clinical development, CRO scientific affairs, health outcomes consultancy, academic research in psychometrics or patient-reported outcomes, or regulatory science. Postgraduate degree (MSc, PhD, or equivalent) in clinical outcomes research, psychometrics, health economics and outcomes research (HEOR), epidemiology, clinical psychology, or a closely related discipline.
Labcorp Holdings IncScientist II - Clinical Genomics Labcorp Holdings IncScientist II - Clinical GenomicsIselin, NJRemote$90,000ā$129,000 / yearThis role is heavily focused on hands-on laboratory work, with the primary responsibility centered on the technical execution of complex R&D experiments, design and execution of validation studies, and continuous improvement of existing assays and workflows. The ideal candidate will bring deep expertise in next-generation sequencing (NGS) and other high-complexity genomic technologies, along with strong analytical and technical writing capabilities.
Summit Health IncClinical Lab Scientist - Core Lab (Generalist) Summit Health IncClinical Lab Scientist - Core Lab (Generalist)Woodland Park, NJ$31.59ā$39.52 / hourOur primary, multispecialty, and urgent care providers serve millions of patients in traditional practices, patients' homes and virtually through VillageMD and our operating companies Village Medical, Village Medical at Home, Summit Health, CityMD, and Starling Physicians. We are innovating value-based care and leveraging integrated applications, population insights and staffing expertise to ensure all patients have access to high-quality, connected care services that provide better outcomes at a reduced total cost of care.
KenvueNewPre Clinical Safety Data Scientist KenvuePre Clinical Safety Data ScientistSummit, New JerseyD. ( preferred) in Data Sciences, Computational & Integrative Sciences or equivalent , with proven track record (e.g publications, posters, presentations) of applying modeling, simulation, and computational approaches for real world academic or industry toxicology/health sciences studies . In this role, you will leverage advanced computational, omics, and data science approaches to support pre-clinical safety and product development decisions, integrating AI and machine learning tools to accelerate insights and enhance scientific workflows.
CVS Health CorpSenior Data Scientist - Clinical Informatics (Analytics Enablement) CVS Health CorpSenior Data Scientist - Clinical Informatics (Analytics Enablement)NY$101,970ā$203,940 / yearExperience designing patient-centric data models, feature stores, and dashboards that aggregate longitudinal data across sources, including demographics, encounters, conditions, medications, labs, utilization, cost, and enrichment attributes. A&BC leverages advanced analytics, clinical informatics, and hypothesis-driven approaches to transform data into actionable, customer-centric insights that drive growth, improve health outcomes, and expand access to healthcare across all CVS Health businesses.
CVS Health CorpData Scientist - Clinical Informatics (Analytics Enablement) CVS Health CorpData Scientist - Clinical Informatics (Analytics Enablement)NY$79,310ā$158,620 / yearA&BC leverages advanced analytics, clinical informatics, and hypothesis-driven approaches to transform data into actionable, customer-centric insights that drive growth, improve health outcomes, and expand access to healthcare across all CVS Health businesses. Experience designing patient-centric data models, feature stores, and dashboards that aggregate longitudinal data across sources, including demographics, encounters, conditions, medications, labs, utilization, cost, and enrichment attributes.
CVS Health CorpData Scientist - Clinical AI CVS Health CorpData Scientist - Clinical AINY$79,310ā$158,620 / yearWork with machine learning engineers, data engineers, clinical informaticists, and business partners to ensure clinical data pipelines support AI/ML workflows and that model outputs are integrated into products and decision-making processes. A&BC leverages advanced analytics, clinical informatics, and hypothesis-driven approaches to transform data into actionable, customer-centric insights that drive growth, improve health outcomes, and expand access to healthcare across all CVS Health businesses.
Prime Healthcare Services IncClinical Laboratory Scientist I Prime Healthcare Services IncClinical Laboratory Scientist IDenville, NJ$28ā$37.68 / hourEach individual performing the above procedures must: 1) adhere to the laboratorys procedures for the collection, processing, analysis, and reporting of patient test results, 2) follow the laboratorys established quality control policies and procedures in documenting all corrective actions taken when test systems deviate from the laboratorys established performance specifications, 3) be capable of identifying problems that may adversely affect test performance and either correct the problem or immediately notify your immediate supervisor, Director, or Medical Director, 4) perform a wide variety of laboratory procedures requiring independent judgment using both manual and automated methods in Hematology, Blood Bank, Chemistry, Urinalysis, Coagulation, Microbiology, Immunology, and any other discipline as introduced into the laboratory, 5) perform and document maintenance daily, weekly, monthly, or as needed on instruments and equipment as appropriate, 6) review the accuracy of patient results prior to releasing or reporting, 7) recognize age specific differences in expected results for newborns to geriatrics, 8) ensure that the testing of proficiency testing samples are tested in the same manner as patient samples and that collaboration with other laboratories is prohibited prior to the reporting of proficiency testing results to the appropriate agencies, 9) may be required to perform venipuncture or capillary puncture on various age groups from newborn to geriatrics, 10) assist in the development and maintenance of laboratory policies and procedures, 11) adheres to all department and hospital policies and procedures related to safety, infection control, emergency preparedness, and human resources, 12) in the absence of a supervisor, may be assigned/identified as Lead Tech, having responsibility for the section or department during their shift, 13) may be assigned responsibilities related to LIS and/or POCT. Saint Clare''s Health includes CMS 5-Star Rated hospitals and is an award-winning provider of safe, high quality, compassionate care, serving the communities of Morris, Warren and Sussex counties.
St. Clare's - DenvilleClinical Laboratory Scientist St. Clare's - DenvilleClinical Laboratory ScientistDenville, New Jersey$28ā$37.68 / hourEach individual performing the above procedures must: 1) adhere to the laboratorys procedures for the collection, processing, analysis, and reporting of patient test results, 2) follow the laboratorys established quality control policies and procedures in documenting all corrective actions taken when test systems deviate from the laboratorys established performance specifications, 3) be capable of identifying problems that may adversely affect test performance and either correct the problem or immediately notify your immediate supervisor, Director, or Medical Director, 4) perform a wide variety of laboratory procedures requiring independent judgment using both manual and automated methods in Hematology, Blood Bank, Chemistry, Urinalysis, Coagulation, Microbiology, Immunology, and any other discipline as introduced into the laboratory, 5) perform and document maintenance daily, weekly, monthly, or as needed on instruments and equipment as appropriate, 6) review the accuracy of patient results prior to releasing or reporting, 7) recognize age specific differences in expected results for newborns to geriatrics, 8) ensure that the testing of proficiency testing samples are tested in the same manner as patient samples and that collaboration with other laboratories is prohibited prior to the reporting of proficiency testing results to the appropriate agencies, 9) may be required to perform venipuncture or capillary puncture on various age groups from newborn to geriatrics, 10) assist in the development and maintenance of laboratory policies and procedures, 11) adheres to all department and hospital policies and procedures related to safety, infection control, emergency preparedness, and human resources, 12) in the absence of a supervisor, may be assigned/identified as Lead Tech, having responsibility for the section or department during their shift, 13) may be assigned responsibilities related to LIS and/or POCT. Saint Clare's Health includes CMS 5-Star Rated hospitals and is an award-winning provider of safe, high quality, compassionate care, serving the communities of Morris, Warren and Sussex counties.
St. Clare's - DoverNewClinical Lab Scientist II St. Clare's - DoverClinical Lab Scientist IIDover, New Jersey$29.12ā$39.19 / hour3) be capable of identifying problems that may adversely affect test performance and either correct the problem or immediately notify your immediate supervisor, Director, or Medical Director, 4) perform a wide variety of laboratory procedures requiring independent judgment using both manual and automated methods in Hematology, Blood Bank, Chemistry, Urinalysis, Coagulation, Microbiology, Immunology, and any other discipline as introduced into the laboratory, 5) perform and document maintenance; daily, weekly, monthly, or as needed on instruments and equipment as appropriate, 6) review the accuracy of patient results prior to releasing or reporting, 7) recognize age specific differences in expected results for newborns to geriatrics, 8) ensure that the testing of proficiency testing samples are tested in the same manner as patient samples and that collaboration with other laboratories is prohibited prior to the reporting of proficiency testing results to the appropriate agencies, 9) may be required to perform venipuncture or capillary puncture on various age groups from newborn to geriatrics, 10) assist in the development and maintenance of laboratory policies and procedures, 11) adheres to all department and hospital policies and procedures related to safety, infection control, emergency preparedness, and human resources, 12) in the absence of a supervisor, may be assigned/identified as Lead Tech, having responsibility for the section or department during their shift, 13) may be assigned responsibilities related to LIS and/or POC. Saint Clare's Health includes CMS 5-Star Rated hospitals and is an award-winning provider of safe, high quality, compassionate care, serving the communities of Morris, Warren and Sussex counties.
Prime Healthcare Services IncClinical Laboratory Scientist III Prime Healthcare Services IncClinical Laboratory Scientist IIIDover, NJ$30.28ā$40.76 / hourThis individual: 1) functions as the department Section Supervisor or Lead, responsible for supervising the daily operation of the section(s), 2) provides consultative services to the medical staff in the capacity of Technical Consultant, 3) oversees the section/department performance improvement program and participates in hospital interdisciplinary performance improvement initiatives, 4) is responsible for the technical and fiscal management of the section(s), 5) oversees the section(s) quality management/assurance program, 6) ensures compliance with all regulatory and accreditation requirements, 7) assesses staff competency and completes performance evaluations in a timely manner,8) ensures the accuracy of patient results prior to releasing or reporting, 9) develops, maintains and updates section policy and procedure manuals, 10) reviews quality control performance ensuring documentation of corrective actions taken when test systems deviate from the laboratory's established performance specifications, 11) identifies problems that may adversely affect test performance and either correct the problem or immediately notify the, Director, or Medical Director, 12) performs a wide variety of laboratory procedures requiring independent judgment using both manual and automated methods in Hematology, Blood Bank, Chemistry, Urinalysis, Coagulation, Microbiology, Immunology, and any other discipline as introduced into the laboratory, 13) ensures the performance and documentation of equipment maintenance - daily, weekly, monthly, or as needed, 14) recognizes age specific differences in expected results for newborns to geriatrics, 15) ensures that the testing of proficiency testing samples are tested in the same manner as patient samples and that collaboration with other laboratories is prohibited prior to the reporting of proficiency testing results to the appropriate agencies, 16) ensures the currency of all laboratory policies and procedures, 17) adheres to all department and hospital policies and procedures related to safety, infection control, emergency preparedness, and human resources, 18) may be assigned responsibilities related to LIS and/or POC. Saint Clare''s Health includes CMS 5-Star Rated hospitals and is an award-winning provider of safe, high quality, compassionate care, serving the communities of Morris, Warren and Sussex counties.