R & D Jobs in Summit, New Jersey

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241 Summit, NJ R & D jobs found on Monster.

Jobs 1 to 20 of 241
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...
This is a highly collaborative role, working in a matrixed organization of commercial, veterinary operations and academic specialty colleagues. This role is the primary marketing interface charged with the development of effective strategic partnerships with national/international level companion animal veterinary Key Opinion Leaders. This individual will make sure companion animal brands and init...
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...
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...
Seeking multiple Project Managers for consulting positions at a major pharmaceutical client in East Hanover, NJ 07936. Key components of the responsibilities are as mentioned below: · Manages projects from scope definition to deployment · Liaisons with internal and external client’s · Defines project scope, approach and understands client reporting requirements for adverse events · Creates strateg...
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: *****...
Our client, a large pharmaceutical company, is currently seeking a DESKTOP PUBLISHER. Responsible for publishing and managing QC for high quality scientific documentation (e.g. study reports) for submission to regulatory authorities in support of marketing applications Preparation of high quality scientific documentation and submission documents in accordance with the timelines specified by NIBR a...
*BA/BS or advanced degree required! 3 years of experience required!* Duties: The team is looking for highly motivated and pleasant individuals with previous experience a clinical trial site in a global pharma company or those with experience in conducting a global study. We have a strong preference for those with a strong scientific or clinical background (i.e., oncology nurse, pharmacists, etc) a...
Hello, My name is Bryson Jackson and I represent The Fountain Group. We are a national staffing firm and are currently seeking a Desktop Publisher (s) for a prominent client of ours. This position is located in East Hanover, NJ. Details for the positions are as follows: Job Description: LONG TERM CONTRACT!!!! FORTUNE 500 CLIENT!!!! Duties Responsible for publishing and managing QC for high quality...
Desktop Publisher – 6 month contract Responsible for publishing and managing QC for high quality scientific documentation (e.g. study reports) for submission to regulatory authorities in support of marketing applications. Preparation of high quality scientific documentation and submission documents in accordance with the timelines specified by Novartis Institutes for BioMedical Research (NIBR) and...
The Fountain Group has an IMMEDIATE opening for a Clinical Research Scientist in east Hanover, NJ. Qualified candidates should submit an updated resume along with contact information to be considered. Overview The team is looking for highly motivated and pleasant individual with previous experience at a clinical trial site in a global pharma company or those with experience in conducting a global...
Clinical Research Manager II – 6 month contract Support US efforts in the planning, execution and reporting of US Clinical Data and Medical Affairs (CDMA) clinical trials in Oncology: Implementation of clinical trials in the United States (safety, data consistency, trial timelines, budget, resources, eligibility and enrollment), within a cross functional team and with oversight from the Associate...
Biostatistician III – 6 month contract Designing clinical studies. Writing and reviewing statistical sections and other relevant parts of study synopses and protocols. Support study start up activities. Develop RAP, program TLFs, preparation for database lock, dry run and CSR activities. Review CRF, DB spec, VAP. Support analyses as required for decision making at project level. Support analyses a...
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