R & D Jobs in Newark, New Jersey

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200 Newark, NJ R & D jobs found on Monster.

Jobs 1 to 20 of 200
Type : Front-Line, Experienced Position Summary : The Principal Statistical Programmer is responsible for all programming aspects (including analysis datasets, pooled datasets, tables, listings, and figures) of individual Phase I – IV clinical trials and project level activities for drug/Life Science projects. The Principal Statistical Programmer provides technical expertise to offer consulting, t...
Key Activities : Statistical programming Providing support for creating and maintaining programs to analyze and report clinical trials data. o Create or review data specifications. o Program or validate derived datasets, tables, listings and graphs Providing quality control for study documents, programs and outputs of statistical programs Effectively contribute to department study teams. study Qua...
The incumbent will have the overall management and study site monitoring of clinical sites, which include conduct of pre-study and initiation visits, interim monitoring, and close out visits in accordance with company standard operating procedures. The incumbent will also have on and off-site monitoring responsibilities that include ensuring study staff has received proper training to conduct the...
The Brand Lead, reporting directly into the head of New Products North America, defines and develops the strategic platform for new compounds within Diabetes. The brand lead has ownership of the asset beginning at phase IIb to early phase III and owns the development of the North America initial customer perspective products lifestyle, launch road map and launch preparation up to the eventual tran...
We have been retained by one of the world's leading manufacturers of medical/surgical disposable products to assist them as they expand their sales organization. You will be responsible to manage your own N. New Jersey Territory for their existing business and develop new sales primarily in the acute care market. With products that are clinically superior, you will call on various departments of t...
PRINCIPAL SDTM PROGRAMMER *This remote opportunity is open to any US home-office location. Theorem Clinical Research is currently searching for experienced SDTM Programmers. In this role, the SDTM Programmer will be responsible for mapping entire studies in accordance with SDTM guidelines, as well as performing Quality Control checks. RESPONSIBILITIES: Create SAS datasets of clinical data from cli...
Position: Senior Decision Analytics Consultant “Emphasis is on end product delivery of analysis and guiding junior staff” Role: · Contribute and guide the team on structural analysis of the project Contribute and guide the team on insights from conclusions of analysis that integrate with initial hypothesis and business objective · Independently address complex problems · Participate in design of m...
Our client is the world's leading chemical company. With more than 110,000 employees, six affiliate sites and approximately 380 additional production sites worldwide they serve customers and partners in almost all countries of the world. They combine economic success, social responsibility and environmental protection. Through science and innovation they enable customers in almost all industries t...
CHIEF CHEMICAL OPERATOR- Bayonne NJ Vertellus is a dynamic international company with more than a century of leadership in the manufacture of health, agriculture and performance chemicals. Vertellus Performance Materials Inc., located in Bayonne, NJ, specializes in the production of Castor Oil based specialty chemicals. We currently seek a Chief Chemical Operator to perform various tasks essential...
PhD in either Glass Science, Ceramic Engineering, Inorganic Chemisty or Materials Science 1-2 years experience. The R & D team located in Union, NJ performs research on conductive materials and technologies used in photovoltaics, displays and other electronics applications. Responsibilities include but are not limited to: -Perform Research and Development activities in the field of glass science....
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...
LOOKING TO MAKE A MOVE TO CONSULTANCY? ANALYST / SENIOR ANALYST POSITION COMPANY PROFILE Medical Marketing Economics (MME) is a strategic advisory company to the global bio-pharmaceutical industry, focused on helping clients identify, frame, communicate and capture the value of their products while gaining timely and appropriate market access. We are driven by intellectual curiosity and are passio...
Job Responsibilities: · Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites for GCP compliance according to PharmaNet SOPs and/or client guidelines · Generate study specific documentation including monitoring trip reports, telephone contact reports, site correspondence and expense reports · Recruit investigators for participation in clinical trials · Conduct projec...
Position Purpose: The Senior Associate Regulatory Affairs will play a key role in the US Regulatory Affairs efforts to seek the approval of new applications and the maintenance of approved applications as required by the US-FDA Regulations and applicable guidances. The successful candidate will work with minimal supervision and when necessary, within a team setting to support regulatory goals dete...
The Senior Clinical Contracts Manager (SCM) is responsible for assisting the clinical project teams with clinical vendor negotiation and executing all study contracts. This individual helps to prepare Clinical Trial Agreements and ultimately manages the contractual agreements. Develops study specific agreements and patient budgets with clinical study team. Manages requests for vendor proposals, an...
Our client, located in Bergen County, NJ is a leader in DNA-based cancer diagnostics and clinical management. They are seeking to fill the immediate role of Senior Clinical Trial Project Associate. Candidates must be able to work independently and as a team. They must have the following qualifications: Strong experience with clinical data management, analysis and reporting Thorough understanding o...
Role Title: MFT Analytical - Process Chemist Role Function and Group: Manufacturing Technology Analytical – Sales and Supply Location: Linden Position Summary: This position reports to the Manufacturing Technology Manager – Analytical. The primary purpose of this role is to take a leading role in experiment planning, data analysis and reporting for MFT analytical test method and Process Analytical...
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...
Functions/Responsibilities: Develop, maintain, and implement new and existing technologies for brand protection Lead a multi-disciplinary technical team Maintain and improve existing technologies and products. Includes communications with customers and overseeing customer needs as required Develop new products based on existing technologies (internal or external) for expansion and/or improvement o...
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...
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