R & D Jobs in Cranford, New Jersey

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181 Cranford, NJ R & D jobs found on Monster.

Jobs 1 to 20 of 181
Clinical and Regulatory Analyst - III Must have: - Bachelor's degree, preferably in nursing, pharmacy or a biological science - At least three years of experience in a hospital, pharmaceutical, or research position. - Prior experience in coordinating and overseeing the production of Aggregate Reports (PSUR, DSUR, PAER etc.) and RMPs required. - PSUR authoring experience would be considered. ...
At Joulé, you could say the right match is in our DNA. We're the specialists in Scientific Staffing. Our unmatched industry network and geographic reach enable us to place professionals like you at top firms every day. For more than 20 years, we've been providing temporary, contract and direct staff to pharmaceutical, biotechnology, food, flavor and fragrance, specialty chemical and other scientif...
Currently we have a temporary opening for a Facilities Engineer to support a company located in the Short Hills, NJ area.   Responsibilities: Manage major construction projects at multiple North American sites. Developing design concepts with the users and design engineering firm Developing request for proposals to bid projects, coordination with customers, contractors and consultants, Revie...
Company Confidential Edison, NJ, 08837
POSITION SUMMARY: The incumbent will manage all activities of the Quality function and have overall hands-on responsibility for the development, deployment, administration and maintenance of quality systems and product control internally and at Contract Organization encompassing Biologic and Radiologic development programs. ESSENTIAL DUTIES AND RESPONSIBILITIES: Responsibilities include, but ar...
Responsibilities · Propose annual financial goals and upon management approval, review quarterly performance and make necessary adjustments to ensure accomplishing the yearly goals · Develop research partnership in therapeutic proteins including both biobetter and bioinnovative entities. · Reach out to customers and connect their demands of in vitro and in vivo pharmacology to GenScript’s high ...
Summary Regional Marketing and Service Marketing Manager has responsibility for executing regional marketing strategy including tradeshow and eMarketing campaigns for all reagent service lines. In addition, this position is responsible for planning and implementing global molecular cloning service strategy. Location This position is based in Piscataway, New Jersey. Number of direct reports: 1 ...
Location: Piscataway, NJ, US Job Description: Technical Account Manager serves as the primary technical source for supporting sales activities within responsible regions. Technical Account Managers take full responsibility of the daily operation of customer service function, which handles all initial inquiries from customers, dealers, and general public regarding order placement, complaints, tec...
CLINICAL SPECIALIST MANAGER JOB RESPONSIBILITIES 1. Create/Manage a team of clinical specialists to become experts of Nuclear Cardiology and particularly in Cardiac PET, Lung and Endocrine disease Diagnostics 2. Create the process and manage the resources required for set-up and installation of the Rubidium Elution System (RbES) and Ruby-Fill™ generator and ensure proper troubleshooting procedu...
CorePharma LLC is a fast growing mid-size generic pharmaceutical company with approximately 250 employees, located in Middlesex, New Jersey. We are a fourteen year old firm principally in the business of developing, manufacturing, and distributing pharmaceutical products for the United States market. JOB SUMMARY: Under the direct supervision of the Supervisor, Quality Control Laboratory, the inc...
Responsibilities: · Support the MRL clinical monitors (physicians) who oversee the conduct of Phase I clinical trial. Various therapeutic areas (NON ONCOLOGY) · Lead a team of functional area members through the end-to-end process of PHASE I study conduct (normal healthy volunteer, PK/PD, DDI, ADME, special populations) · Order study related supplies Oversee CRO management for sourced Phase I t...
This position is responsible for statistical planning and data analysis of Clinical Trials, in particular Early Phase biomarker studies and Clinical Pharmacology trials. Senior Scientist, Biostatistics Rahway, NJ Job # BIO004013 - Requires a solid knowledge of Statistical Methodology, Experimental Design, and some knowledge in computing software and data management. - Knowledge must be suffic...
Medical Writer/Clinical - III Location: Rahway, NJ OR Upper Gwynedd, PA Must have: Education: Bachelor’s Degree required. RN degree, PhD in health related field and/or PharmD is a plus. Skills: • Must have at least 4 years of medical writing experience within the pharmaceutical industry and at least 2 years of this experience must have been spent authoring clinical documents for regulatory su...
Company Confidential Summit, NJ, 07901
We are seeking a research scientist with proven success at the bench. Possesses a strong understanding of science behind ongoing experiments: the rationale, purpose and appropriate analytical methods. The position holder works virtually independently toward defined objectives conducting several complex experiments, some in parallel, and offering insight into future experiments. The scientist displ...
Requirements: -Minimum 5 years experience within biotech/CRO working in-house performing duties of a CRA -Experience in locking a database is required -CRO/Vendor Management is required -Ophthalmology is plus -Monitoring experience is a plus Responsibilities: 1.Support the trial operation activities in accordance with country specific regulations/GCPs and companies SOPs 2.Responsibilities ...
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries - and growing - we l...
Qualifications: Minimum of a BS degree Regulatory experience preferred Pharmaceutical/Biological manufacturing or Quality experience preferred Experience preparing CMC (Chemistry, Manufacturing, Controls) post approval submissions preferred Experience with Trackwise and regulatory tracking databases preferred Proactive and highly productive Sound judgment Attention to detail Strong writte...
TechData is looking for Biostatistician, Outcome Research Biostatistician,SAS Programmer/Statistical Programmer (Some can be telecommuting), Translational Operation Manager, Outsourcing Manager, Drug Safety Specialist/Trial Safety Manager, Clinical Study Manager/Clinical Research Scientist, Sr. Clinical Data Manager for our pharmaceutical clients in Central NJ and Northern NJ. Please see below req...
Manager, Trials Safety Surveillance • To provide excellent safety support to Development and Marketed product studies • To assist medical affairs teams and the lead safety MD in identifying and managing safety concerns • To ensure effective safety surveillance across trials • To draft safety sections of key trial documents Responsible for: • Identifying and assisting in the management of saf...
Manage projects/engagements delivering sales, marketing and managed markets solutions. Familiarity with the application of analytics to sales and marketing problems such as: • Commercial model design, Sales Force Sizing, Territory Alignment, Sales Call Planning, Incentive Compensation. • Market segmentation, marketing program ROI, marketing mix optimization. • Managed markets pull through anal...
Peak Environmental Inc. is looking to add staff members to our environmental consulting company to address our expanding workload in the areas of environmental site assessments, investigation and remediation. This is a unique opportunity for growth at any level. Entry level candidates will find a wide variety of interesting projects to participate in; mid level candidates will find increased proje...

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