Associate Director, Data Science Princeton UniversityAssociate Director, Data SciencePrinceton, New Jersey$145,000–$160,000 / yearFull timeDescribe findings or the way techniques work to audiences, both technical and non-technical, effectively using presentation tools such as data visualization, PowerPoint and documentation to drive strategic decision making and understanding of business analytics at all levels of the organization. Data Strategy and Innovation plays a critical strategic role within Advancement, providing the analytical framework, data architecture, application development, and tools for data-driven decision making at all levels of the organization.
Clinical Scientist SystimmuneClinical ScientistPrinceton, NJFull timeWork in close collaboration with the clinical team to ensure translation of the clinical protocol (and amendments) into operational deliverables, including but not limited to performing ongoing review and analysis of clinical study data and preparing/reviewing study plans (i.e., Medical Monitoring, Medical Data Review, Safety Management, CRF Completion Guidelines, etc.). This role provides an excellent opportunity to gain hands-on experience in clinical trial design and execution while working alongside experienced clinical development professionals in a dynamic biotech/pharmaceutical environment.
Soil Scientist Dynamic Engineering Consultants, PCSoil ScientistNewtown, PennsylvaniaFull timeResponsibilities: Perform routine and complex field exploration programs for a wide range of project types including, but not limited to determination of Seasonal High Water and/or Groundwater levels, USCS and USDA soil classification and logging, rock core classification and logging, hydraulic conductivity and/or percolation testing, and groundwater well installation. American Concrete Institute (ACI) concrete field-testing technician certificate, accredited construction inspection/materials testing certificates, OSHA 40, OSHA 10, and/or American Portable Nuclear Gauge Association (APNGA) gauge training preferred.
NewAssociate Director, Clinical Project Scientist 6120-Janssen Scientific Affairs Legal EntityAssociate Director, Clinical Project ScientistHorsham, PennsylvaniaAgile Decision Making, Agility Jumps, Analytics Insights, Business Alignment, Continuous Improvement, Cross-Functional Collaboration, Leadership, Organizational Project Management, Organizing, Program Management, Project Management Methodology (PMM), Project Management Office (PMO), Project Management Tools, Project Reporting, Statement of Work (SOW), Technical Credibility . Additionally, candidate will need to act as point of contact with external Investigators and/or collaborative groups for protocol intake/review, contract/budget negotiations, track clinical supply demand, manage and track protocol deliverables, including data generation activities (study reports, manuscripts, congress publications).
Environmental Scientist - 2 years minimum experience AECOMEnvironmental Scientist - 2 years minimum experienceBloomfield, NJ$65,000–$85,000 / yearWe invite you to bring your bold ideas and big dreams and become part of a global team of over 50,000 planners, designers, engineers, scientists, digital innovators, program and construction managers and other professionals delivering projects that create a positive and tangible impact around the world. **ReqID:** J10155409 **Business Line:** Environment **Business Group:** DCS **Strategic Business Unit:** West **Career Area:** Science **Work Location Model:** On-Site **Compensation:** USD 65000 - USD 85000 - yearly
Senior Scientist I, Bioanalytical WuXi AppTecSenior Scientist I, BioanalyticalCranbury, New JerseyOverview: The Senior Scientist I is responsible for the day-to-day coordination and supervision of the team operation to ensure the successful implementation of the DMPK Non-GLP Bioanalytical method development, method qualification, sample analysis, report writing, and metrics in order to deliver outstanding customer satisfaction in the field of drug discovery and development. An expert in the use of advanced experimental methods, concepts and techniques relevant to scientific discipline and specific area, such small or large molecule bioanalytical, including LC-MS, ELISA/MSD, PCR, flow cytometry, western blotting, etc, Demonstrated experience in the independent development of LBA and/or LC-MS bioanalytical methods.
Upstream Process Development Scientist Integrated Resources, IncUpstream Process Development ScientistSouth Plainfield, New JerseyFull timeindustrial experience and for a candidate with a BS, >7 years of industrial experience in developing upstream microbial fermentation processes for the production of bio-pharmaceuticals is required. Lead efforts to evaluate different fermentation media, feeds, and feeding strategies to improve product yield and quality including proper folding of protein.
Scientist, Quality Control (2Nd/3Rd Shift) Orca BioScientist, Quality Control (2Nd/3Rd Shift)Princeton, NJ$70,000–$90,000 / yearProduction Associate Roles: Must have visual acuity of 20/20 (corrected or uncorrected) and normal color vision to safely perform critical tasks such as visual inspection of materials, equipment, and labeling, including distinguishing color-coded components in a GMP environment. The Scientist, Quality Control conducts routine and non-routine analysis, including but not limited to biochemical and chemical analysis of processes leading up to drug product according to established operating procedures.
Director, Pharmacovigilance Scientist Bristol Myers SquibbDirector, Pharmacovigilance ScientistPrinceton, NJ$217,520–$263,577 / yearRisk Management Planning & Execution: Creates strategy for creation and update of the EDSR to proactively characterize emerging safety concerns during asset development, support Structured Benefit Risk, and define the strategy for Company Core Risk Management and gaining alignment with SMT/governance, including collaboration with Epidemiology on risk minimization effectiveness, non-interventional research (NIR) activities for post-authorization safety studies (PASS). The Director, Patient Safety Scientist, is a key partner and strategic advisor to Medical Safety Assessment Physician (MSAP)/Safety Management Team (SMT) Chair to characterize conditions for safe use of BMS medicines and proactively communicate safety evidence to influence decision-making for assets in development and marketed products by evaluating and mitigating risks.
NewAssociate Director, Clinical Project Scientist Johnson & JohnsonAssociate Director, Clinical Project ScientistHorsham, PennsylvaniaAgile Decision Making, Agility Jumps, Analytics Insights, Business Alignment, Continuous Improvement, Cross-Functional Collaboration, Leadership, Organizational Project Management, Organizing, Program Management, Project Management Methodology (PMM), Project Management Office (PMO), Project Management Tools, Project Reporting, Statement of Work (SOW), Technical Credibility . Additionally, candidate will need to act as point of contact with external Investigators and/or collaborative groups for protocol intake/review, contract/budget negotiations, track clinical supply demand, manage and track protocol deliverables, including data generation activities (study reports, manuscripts, congress publications).
Associate Director, Patient Safety Scientist Bristol Myers SquibbAssociate Director, Patient Safety ScientistPrinceton, NJ$150,300–$182,125 / yearResponsible for creation and update of the EDSR to proactively characterize emerging safety concerns during asset development, support Structured Benefit Risk, and define the strategy for Company Core Risk Management and gaining alignment with SMT/governance, including collaboration with Epidemiology on risk minimization effectiveness, non-interventional research (NIR) activities for post-authorization safety studies (PASS). The Associate Director, Patient Safety Scientist, is a key partner and strategic advisor to Medical Safety Assessment Physician (MSAP)/Safety Management Team (SMT) Chair to characterize conditions for safe use of BMS medicines and proactively communicate safety evidence to influence decision-making for assets in development and marketed products by evaluating and mitigating risks.
Principal Scientist, Cell Line Genome Engineering Bristol Myers SquibbPrincipal Scientist, Cell Line Genome EngineeringPrinceton, NJ$135,800–$164,563 / yearExtensive hands-on and strategic experience with CRISPR-based genome engineering technologies (e.g., Cas9, Cas12a, dCas9, base-editing, prime-editing and related systems), and gene delivery methods (lentiviral, AAV, electroporation, transposon), with a proven track record of leveraging these tools to build, scale, and optimize cellular models that advance discovery programs. Demonstrated expertise in the design and generation of genetically engineered cellular systems (e.g., knockouts, knock-ins, targeted insertions, overexpression) using a range of approaches including CRISPR-based editing, viral delivery systems, and transposon-based technologies, with the ability to apply these strategically to drug discovery challenges.
Scientist - I Net2SourceScientist - IRahway, NJ$32–$32.14 / hourRequired Skills and Experience Must have separations experience for small molecules/peptides Experience in analyzing small molecule formulation development samples and/or other therapeutic modalities using at least one of the following techniques: Liquid Chromatography (HPLC / UPLC) Such as: Size Exclusion Chromatography (SEC), Ion Exchange Chromatography (IEX, AEX, CEX), Reverse Phase (RP), or Hydrophobic interaction chromatography (HIC). Key must-have skills: Experience with liquid chromatography , including running instruments, preparing samples, collecting/processing data, and understanding chromatography modes.
Clinical Project Scientist Integrated Resources, IncClinical Project ScientistRaritan, New JerseyContractorScope of responsibility includes: In concert with the Associate Director, Clinical Project Scientist, the contractor CPS will direct the overall coordination and management of CVM MA clinical studies including: working in a highly matrix organization, the contract CPS will play a key role in interfacing with our partners to contribute to concept and protocol development, drive accurate budget forecasting and communicate variances, provide project management across the study to drive metrics and alignment to timelines, facilitate critical path analyses and optimization/contingency planning, escalate issues as appropriate for timely resolution, provide updates to senior management as directed. The Clinical Project Scientist (CPS) is a key interface role in the CVM Medical Affairs (CVM MA) organization responsible for collaborating with therapeutic area teams to act as a liaison between therapeutic strategy and the clinical and operational implementation of product programs and clinical studies.
Scientist -IV (Reagent Development) Integrated Resources, IncScientist -IV (Reagent Development)Raritan, New JerseyContractorThe candidate will be independently responsible for optimizing instrument related solution preparation, developing commercial –ready process based upon R&D processes, scaling up reagent production, validating assay reagent production and transferring production processes. The successful candidate will be responsible for designing and improving processes for reagent manufacturing, independently reviewing manufacturing procedures and execute experimental processes, as well as serving as technical representative in transferring new products.
Sr. Scientist Formulation Integrated Resources, IncSr. Scientist FormulationSouth Brunswick, New JerseyFull timeMust have experience in developing oral solid dosage forms from Bench Scale all the way to large scale submission batch manufacture, at other generic Pharma companies. • Formulator with previous industrial experience developing generic Oral Solid Dosage Forms (including Oral Liquids preferred).
Senior Scientist, Analytical Chemistry Amneal Pharmaceuticals, Inc.Senior Scientist, Analytical ChemistryBranchburg Township, NJThe individual is a part of the Quality Control Technical Services team which develops, validates/verify, and qualifies testing methods for active pharmaceutical ingredients, excipients and dosage forms, including troubleshooting and lifecycle management of analytical methods. Description: The Senior Scientist, Analytical Chemistry fulfills a critical role in supporting the analytical development and validation/verification and method transfer of testing methods for the Quality control laboratory, to characterize drug substance, raw materials, and drug products.
Scientist-IV Integrated Resources, IncScientist-IVRaritan, New JerseyContractorD. degree with post-doctoral experience and 3+ years performing progressively advanced duties or an MS degree and a minimum of 10 years of experience or a BS degree and a minimum of 15 years of experience performing progressively advanced duties beyond a B.S. degree, or at least 3 years of experience performing progressively advanced duties at the Senior Associate Scientist level, or the equivalent training/experience. Must work by strictly adhering to the regulations and guidelines of all applicable regulatory agencies, such as FDA (QSR/cGMP), OSHA, ISO (including ISO14001), J&J and OCD Health, Safety & Industrial Hygiene.
NewInhalation Senior Scientist, Formulation R&D Amneal Pharmaceuticals, Inc.Inhalation Senior Scientist, Formulation R&DPiscataway, NJDescription: The Research Scientist of R&D is responsible for the designing and development various inhaled dosage forms such as solution, suspension, gel, cream, ointment, sterile products etc. Essential Functions: Provide scientific leadership for the development of generic pharmaceutical inhaled dosage forms such as metered dose inhalers, DPI's and sterile solution suspension etc.
Clinical Scientist, Ophthalmology SanofiClinical Scientist, OphthalmologyMorristown, NJ$148,500–$214,500 / yearThe primary purpose of the Clinical Scientist's position is to assist/support the Clinical Research Director in the medical/scientific contribution for ophthalmology clinical studies, including: supporting operational activities pertaining to protocol development (such as Informed Consent and committee charters), validation and clinical case review of study data, review of study plans and draft study reports/publications for accuracy, literature review and analysis, and preparation of responses for investigators, study teams, ethics committees, or regulatory authorities. Contribute to preparation and/or review of documents related to studies requiring scientific background (submission portfolio, abbreviated protocol/protocol/amended protocol, patient written information, presentations/communications to internal or external partners, study plans, study reports, trial disclosure form).