R & D Jobs in Springfield, New Jersey

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275 Springfield, NJ R & D jobs found on Monster.

Jobs 1 to 20 of 275
9 month contract position for candidates with Nursing background or equivalent experience preferred. Min. Req: Strong verbal/written communication and interpersonal skills as a team player and be willing to work in an environment where individual initiative, accountability to the team, and professional integrity are required. Per manager: prior experience as a clinical research scientist desired w...
The primary responsibility of this position is the setup and maintenance on test cells in support of the Research and Development of catalysts for emissions reduction. JOB RESPONSIBILITIES Under close supervision, the technician will be complete the following: · Install catalyst samples in the exhaust system · Monitor the operation of the engine and document activities through databases in the TS...
QUALIFICATIONS/JOB REQUIREMENTS: The appointee must meet site-specific qualification requirements as appropriate for state, regional and/or country regulations. This position requires one of the following: ü BS/BA in Medical Technology or ü BS in a Biological Science plus a documented minimum of 1 year training or experience as a Medical Laboratory Technologist In all cases certification (ASCP or...
QUALIFICATIONS/JOB REQUIREMENTS: This position requires a knowledge of clinical trials as would normally be acquired through 2-3 years in Specimen Management or other related laboratory positions. Excellent organizational and communication skills required. Basic MS Office applications required and Customer Service experience in a Clinical Lab setting preferred. Job Description: 1. Accountable for...
SUMMARY Our Company, Chemetall is seeking to hire an Associate Chemist. This is an entry level position. The position requires a undergraduate degree from either a Chemistry or Chemical Engineering degree. Recent college grads with less than 1 year of work experience are welcome to apply. Under the Supervision of the Team Leader performs routine testing and reports results. Processes project reque...
Chemetall is a leader in surface treatment chemicals. When you choose Chemetall's products and services, you give all of our hard work and dedication true validation and worth. No matter what your surface treatment goals, a partnership with Chemetall ensures that your needs will be met with the resources of a world-class company and the personalized attention of a local business. Our company is se...
Chemetall Corporate Information As a leader in surface treatment chemicals, our business means the world to us. When you choose Chemetall's products and services, you give all of our hard work and dedication true validation and worth. No matter what your surface treatment goals, a partnership with Chemetall ensures that your needs will be met with the resources of a world-class company and the per...
Job Description: Assist in the management of the day to day operations of clinical trials including coordination and oversight of all CRO/clinical site/vendor activities, liaison between Clinical Operations Manager and CRO, manage scopes of work/budgets/invoice payments. Participate in development of protocol, case report form, CRF guidelines and other study documents. Prepare and/or review regula...
The Sr. Marketing Manager will lead all Marketing efforts related to our client’s genetics and reproductive brands. The incumbent will lead the development of a rolling operational plan, including marketing objectives and strategies, segmentation brand positioning, pricing, brand life cycle planning, distribution, promotion and competitive action for assigned brand. Qualifications include BS or BA...
LGS Innovations, a leader in government telecommunications and network integration, is seeking a Principal Optical Investigator for our Florham Park, NJ location. With nearly 700 employees nationwide – including more than 300 scientists and engineers – LGS Innovations serves Federal Civilian Agencies, the Department of Defense, and the Advanced Programs community. LGS provides relocation packages...
Regulatory Specialist will provide regulatory and quality support to following business segments: (Human Nutrition, Animal Nutrition, Pharma and Flavors and Fragrances) for Fortune 500 company in the chemical industry. Regulatory Specialist (Chemist) Job Responsibilities · Manages and organizes all group and individual Site Audits. · Requires coordination with various site representatives and cust...
OVERALL RESPONSIBILITIES: Evaluates and executes technical service projects in area of paints and coatings for internal and external customers. Formulates paints and construction products that are used to evaluate additives. Develops new aqueous and solvent based additives for enhancing the performance of paints and coatings. Provides solutions to customer problems using Troy additives. Mentors Co...
Regulatory Specialist will provide regulatory and quality support to following business segments: (Human Nutrition, Animal Nutrition, Pharma and Flavors and Fragrances) for Fortune 500 company in the chemical industry. Regulatory Specialist (Chemist) Job Responsibilities Manages and organizes all group and individual Site Audits. Requires coordination with various site representatives and customer...
This position will work with statisticians and other programmers for the ad hoc analysis for the product Nexium by following PCH programming process and Pfizer SOPs as well as the regulatory guidelines. The candidate should have strong SAS programming skills in clinical trials in the environment of the pharmaceutical industry. The candidate should have MS in math, or statistics or computer science...
Candidates MUST be able to complete a 6mo-1 year assignment. Extension past this time is possible but not guaranteed. No OT, No Travel required. All work to be performed onsite in Madison, NJ DESCRIPTION: Performs all SAS programming required for clinical trial analysis and reporting; Ensures that activities and processes performed are conducted according to sponsor requirements; Works closely wit...
OB SUMMARY The Medical Writer will apply analytical skills, functional literacy and expertise in document preparation including Clinical Study Reports, clinical overviews, integrated analyses of safety and efficacy, regulatory briefing books, key sections of the Investigator s Brochure. May also, in collaboration with the Project Team, assess document requirements, complexity, and potential issues...
Strong planning, tracking, and follow-up skills - Proficient in Excell (including ability to understand programming) Job Description: Summary: The Clinical Program Manager will work cross functionally to develop, track and maintain timelines, resource needs and Key Performance Indicators/Key Quality Indicators across clinical development, coordinate clinical program reviews and support the team in...
TechData is hiring for Oracle Clinical Programmer (Inform, SAS, Jreview), SAS/Statistical Programmer(Some positions can be telecommuting), Biostatistician(Some telecommuting), Drug Safety Specialist, Clinical Data Manager/Data Specialist for our pharmaceutical clients in Central NJ.Please see below requirements and send your resume to: *****. TechData is a leading provider f...
Company Confidential Berkeley Heights, NJ, 07922
We have several positions and are eagerly reviewing new candidates. Please submit your resume if you feel you meet the necessary requirements below: The Clinical Trials Associate (CTA) is involved in the conduct of the study and interfaces with the Study Manager and the Study Team. Requirements: BA/BS in directly-relevant discipline or equivalent experience required At least 2 years experience as...
TechData is hiring SAS Programmer (Some positions can be telecommute), Biostatistician(Some can be telecommute), Clinical Research Scientist/Clinical manager, Contract Specialists, Outsourcing Manager, Informed Consent Setup and study start up, Sr. Clinical Data Managerfor our pharmaceutical clients in Northern NJ. Please see below requirements and send your resume to: *****...
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