R & D Jobs in Trenton, New Jersey

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112 Trenton, NJ R & D jobs found on Monster.

Jobs 1 to 20 of 112
BIOANALYTICAL SCIENTIST WITH EXPERIENCE IN DEVELOPING ASSAYS AND PROTEIN LABELING REQUIREMENT #14-01101 RECRUITER: MELISSA GIUSTI JOB LOCATION: LAWRENCEVILLE, NJ OCTOBER 8, 2014 Project Description: Develops and validates assays that analyze bioanalytical samples (blood, plasma, tissue) for drugs, metabolites, biomarkers or immunogenic response Will analyze samples from preclinical and clin...
QUALITY CONTROL ANALYTICAL CHEMIST Bio-Pharm Inc. is a leading manufacturer and supplier of generic pharmaceutical formulations. Reporting directly to the Quality Control Manager, the Analytica Chemist will coordinate with other Quality Control chemists, R&D researchers and formulation specialists and other manufacturing departments to ensure high quality standards are always met. Major Tasks, K...
Firmenich is the world’s largest privately-held flavors and fragrance company with headquarters in Geneva, Switzerland. Our reputation for excellence as a creator and manufacturer of specialty chemicals, flavors and perfumery products is recognized worldwide. From our award-winning fragrances to our irresistible ingredients, our team has been combining experience and innovation to perfume and flav...
SCIENCE PORTFOLIO MANAGER - Princeton, NJ (Project Management - Life Sciences) Autism Speaks is the world's leading autism science and advocacy organization, dedicated to funding research into the causes, prevention and treatments for autism. Since its establishment in 2005, Autism Speaks has funded work in autism research including basic discovery neuroscience, genetic risk factors, treatment d...
Senior Office Administrator The Senior Office Administrator performs a wide range of diverse duties including support to the VP and Research and Development teams; project and office support activities for multiple staff members; project implementation and tracking. RESPONSIBILITIES: Essential Duties and Responsibilities • Creates and maintains project database • Creates web based surveys • ...
R&D Scientist - Perm opportunity The Scientist fulfills a essential role in supporting the analytical development for oral dosage form pharmaceuticals; leads analytical development, qualifications, validations for Active Pharmaceutical Ingredients (API), excipients, dosage forms, testing and release activities and in-process analytical testing services in support of the formulation development de...
Requisition ID 25178BR Title In-House Clinical Research Associate (CRA) Job Category Clinical Trial Management Job Description PURPOSE: Responsible for the support of assigned sites in accordance with Good Clinical Practice (GCP), ICH guidelines, federal regulations and SOPs. Close collaboration with other members within Clinical Trial Management (CTM) and with various representatives within C...
Clinical Pharmacologist/Toxicologist Beta Pharma, Inc is seeking a driven Clinical Pharmacologist/Toxicologistto manage all nonclinical and preclinical affairs, including clinical pharmacology and toxicology development strategy, design and management of nonclinical and preclinical studies. The successful candidate will additionally manage CRO selection and oversee timelines and budgets. Beta Ph...
About Xcenda Xcenda, a business unit of AmerisourceBergen Corporation, is an integrated, world-class health care consulting organization focused on value, reimbursement and patient access. For more than 2 decades, Xcenda has helped global biopharmaceutical companies as well as emerging early-phase firms successfully commercialize innovative medical treatments and technologies in complex and ...
Home-based position- home office set up with this type of experience preferred Full-Time employee position with full health benefits, dental and vision Therapeutic Area Preferred: Oncology, Hematology MS degree in life sciences with cumulative 5 years pharmaceutical industry experience which includes a minimum of 3 years of pharmaceutical clinical operations experience and 2 years of regional s...
inVentiv Health – Transforming Promising Ideas into Commercial Reality Job Title: Director, Document Management & Publishing Job Description: · Direct operations of the Document Management and Publishing, group · Provide regulatory consulting services to clients, in particular with respect to document management, archiving, and electronic publishing · Provide information and/or data to Propos...
SVP/VP Clinical Development, Oncology - Retained Search Report to CMO: Princeton Area - Specialty R&D Pharma Company Summary: A key Executive Management/Leadership opportunity, reporting to the CMO, you will be responsible for leading and providing ongoing clinical perspective to the research and development strategy. The incumbent will lead clinical product development(s), manage the clinical p...
XenoBiotic Laboratories, Inc. (XBL), a GLP-regulated Pharmaceutical Development Contract Research Organization located in central NJ. Primary Duties and Responsibilities: · Under regular close supervision, individual performs routine laboratory techniques. · Receives specific instructions on assigned task and expected results. · Maintains research notebooks in a well-organized manner. All nece...
Responsibilities: XenoBiotic Laboratories, Inc. (XBL), a GLP-regulated Pharmaceutical Development Contract Research Organization located in central NJ, is seeking an experienced autoradiography research professional to lead the QWBA group to conduct studies as well as manage and participate in other preclinical ADME studies. The successful candidate will serve as a Study Director/Group Leader in...
FIELD MEDICAL MANAGER REQUIREMENT #14-01148 RECRUITER: BRIDGET BURNS JOB LOCATION: PLAINSBORO, NJ OCTOBER 17, 2014 Project Description: Position supports the function of Field Medical working both within a therapeutic area(s) and with impact across the function of Field Medical to support the safe and appropriate use of the client’s medicines. Responsibilities Include: Provide assistance in...
MEDICAL INFORMATION MANAGER, FLUENT IN FRENCH REQUIREMENT #14-01062 RECRUITER: MICHELLE ASHEN JOB LOCATION: PLAINSBORO, NJ SEPTEMBER 29, 2014 Project Description: Participate in ongoing comprehensive product / disease area training to serve as Medical Information expert within area of responsibility Ability to communicate on professional level with physicians, nurses, pharmacists, and other...
MUST HAVE: -Must be Pharm.D. with 3-5 years pharmaceutical industry experience -Individual must have appropriate training and sensitivity to legal and regulatory issues for medical information, while meeting compliance standards for Medical information. -Microsoft Office skills -Understanding of specific disease state and pharmacotherapy knowledge in area(s) of responsibility Responsibilities...
GLOBAL CLINICAL PROTOCOL MANAGER - LATE PHASE SPONSORED RESEARCH WITH ONCOLOGY REQUIREMENT #14-00927 RECRUITER: CINDI PISNOY JOB LOCATION: PLAINSBORO, NJ SEPTEMBER 2, 2014 Expected Areas of Competence: General · Manages successful execution and completion of assigned global clinical Phase IIIb/IV publication/medical informing trials within CSR&O Late Phase Sponsored Research unit, in adhere...
Company Confidential East Windsor, NJ, 08520
Overview Responsible for testing of raw materials, establishing impurity and degradation profiles for active bulk drug substance and release testing of drug product produced using Aprecia Pharmaceutical’s proprietary technology. Description of Duties Research, design and create, QC friendly new procedure to achieve cost effective quantitative test methods. Perform analytical method development...
The Richmond Group has recently been engaged by one our top clients, one of the most well-established names in the pharmaceutical industry, to identify a CLINICAL SCIENTIST to join their team and to help develop their next blockbuster drug. Benefits of this Opportunity: Chance to Make a Difference - This position represents a major role in the organization and will help advance candidates throug...

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