Pennington
R & D Jobs in Pennington, New Jersey
152 Pennington, NJ R & D jobs found on Monster.
Biostatistician Large pharmaceutical company in Central NJ has an immediate for a contract Statistician.Role is initially 12 months with the option to be extended.PhD in statistics w/1-5 yrs exp in pharma industry clinical studies or MS statisticsw/3-5+ yrs. exp in pharma industry clinical studies. Clinical pharmacologystudy exp required.Contractor will support clinical pharmacology efforts. Provi...
Large pharmaceutical company in Central NJ has an immediate need for a contract Statistician. PhD in Statistics w/1-5+ yrs of Clinical Statistics experience within a sponsor and/or CRO environment is required. MS Statistics requires 3-5+ yrs of experience within the Clinical Statistics segment. Previous Clinical Pharmacology (PK/PD) study exp strongly preferred. Contractor will provide protocol re...
This individual contributor is responsible for the management of clinical supplies during the execution phase of clinical trials consistent with GMP guidelines with a specific focus on Temperature Management & Control of Clinical Supplies. Responsible for management of all temperature excursions associated to clinical supplies during the trial execution ensuring prompt resolution and compliance wi...
Position Description: The Senior Residue Chemist position combines the knowledge of several scientific disciplines, such as trace-level analytical (residue) chemistry, separation science, method development and validation, and analytical instrumentation, to lead residue projects in plants, animals, food, and the environment associated with new products, new growth technologies, or to defend critic...
CMC Regulatory Specialist Large pharmaceutical company in Central NJ has 4 immediate needs for contract based CMC Regulatory Specialists. 1 opening requires hands on Biologics experience. Roles are approved through year end with the option to be extended. Duties: The candidate will be responsible for preparing global CMC regulatory submissions for COMPANY’ marketed drug products. The position will...
Large pharmaceutical company in Hopewell, NJ has an immediate need for a contract SAS Programmer. 100% onsite. Role is initially 12 months with the option to be extended. Seeking candidates who possess 9+ years of stateside TLG Programming experience within sponsor and/or CRO environments. Must possess experience creating SAS datasets, generating TLGs/reports, validating other programmers' output,...
Large pharmaceutical company in greater Princeton area has an immediate need for a contract SAS Programmer. Seeking candidates who possess 9+ years of stateside TLG Programming experience within sponsor and/or CRO environments. MS grads preferred, but not required. Must possess experience creating SAS datasets, generating TLGs/reports, validating other programmers' output, adhering to CDISC standa...
Johnson & Johnson companies are equal opportunity employers. CLINICAL SUPPLIES DESIGN LEADER- IVRS-4835130329 Description Janssen Pharmaceutical Research & Development, L.L.C., a member of the Johnson & Johnson Family of Companies, is recruiting for a Clinical Supplies Design Leader - IVRS. This position can be based in either Titusville, NJ or Malvern, PA. Janssen Research & Development, L.L.C. d...
Scientific Support (6 month contract) - The Judge Group has a Scientific Support career opportunity available for our prestigious client, a pharmaceutical company located in Hopewell, NJ. W2 only/local candidates only. Scientific Support details – please only respond if you match requirements. W2 only! Must Have: - Thorough understanding of Documentum based applications - Recent experience in the...
Duties/Responsibilities: The Clinical Research Associate will be responsible for monitoring Phase 3 clinical studies. Clinical Research Associate must have Oncology, Leukemia or Hematology experience. Travel would be 40-50%. Has flexibility to work remotely. CRA must have 3 -5 years’ experience. Bachelor’s Degree also required. Great company and benefits!...
External Overview: FMC Corporation is committed to providing employees with ample opportunities to contribute, lead and be recognized as innovators, to look beyond barriers to provide solutions, to be challenged in what they do and to love doing it. FMC is a S&P 500, diversified chemical company serving agricultural, industrial and consumer markets globally for more than a century. As a global lea...
Company Confidential
Princeton, NJ
Senior Research Scientist: The major duties and responsibilities of a Senior Research Scientist include the following: 1. Follows all standard operating procedures, safety and security polices and prescribedGLP and Biomarker and Immunoanalytical Division practices, policies and guidelines; use SOP manual as reference to support work performed. Completes all necessary paperwork related to job dutie...
TRG has recently been engaged by one of our top clients located in New Jersey, a rapidly growing and respected Pharmaceutical organization that is actively seeking qualified candidates for the role of DIRECTOR OF QUALITY to help them with the development of their cutting edge portfolio of pharmaceuticals. ADVANTAGES OF THIS OPPORTUNITY: CHANCE TO MAKE A DIFFERENCE – As Director of Quality you will...
Company Confidential
Princeton, NJ
Senior Technical Director - Biotechnology expertise Primary responsibility for overall Scientific Strategy, capabilities and technology used at all sites. This includes: * Overall responsibility for content for presentations, technical papers, conference and trade show attendance for company. * Leading position representing company ‘s technical capabilities in client visits. Management of Technolo...
Currently we have a temporary opening for a QC Laboratory Services Supervisor to support a Pharmaseutical Company located in Princeton, NJ. Successful candidates will: Perform and supervise in the testing of raw materials, components and products to comply with release requirements Use and maintain instrumentation required for performing all testing (GC, GPC, HPLC and KF Titrator etc.) Review and...
Shall design and develop dosage forms for metered dose inhalers, dry powder inhalers, nasal sprays, and nebulizers. Required Experience: * Design of Experiments. * Solid state characterization: HPLC, UV-VIS, FTIR, Raman, X-ray Powder Diffraction, thermal analysis. * Aerosol and powder characterization: cascade impaction, moisture sorption isotherm, bulk density, surface area, particle size analysi...
Shall design and develop formulations of new transdermal products. Required Experience: * Transdermal patch physical property testing and rheology testing * Transdermal characterization: x-ray powder diffractometry (XRPD), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), and isothermal microcalorimetry (ITMC) * Knowledgeable of scale-up, tech transfer, and process optimiz...
Company Confidential
Princeton, NJ
Job Responsibilities: The Bioinformatics Data Manager will have primary responsibility for the Bioinformatics data lifecycle. S/He will actively manage data exchange with collaborators, leverage both community data and data standards for internal use and develop/adopt/utilize common ontologies to categorize data. S/He will ensure data integrity and the consistency of meta-data across scientific sy...
Currently we have a temporary opening for a Quality Assurance Specialist to support a company located in the Princeton, NJ area. Responsibilities: Write pharmaceutical manufacturing batch records. Process validation protocols and reports. Process development and scale-up reports. Update SOPs pertaining to manufacturing which requires an understanding of manufacturing processes for oral solid dosag...
Company Confidential
Princeton, NJ
Description Working in collaboration with global regulatory and safety (GRS) CMC teams and bioprocess manufacturing/process development technical experts. Creates final drafts of Regulatory documents for submission to GRS and onwards to global Health Authorities. Documents included: BLA, MAA, IND, IMPD, Briefing packs, responses to queries. Develops overall document strategy with GRS and CMC leade...
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©2013 Monster - All Rights Reserved U.S. Patents No. 5,832,497; 7,599,930 B1; 7,827,125 and 7,836,060 MWW - Looking for Monster Cable? - V: 2013.1.5.22-210