R & D Jobs in Clifton, New Jersey - Page 4

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149 Clifton, NJ R & D jobs found on Monster.

Jobs 61 to 80 of 149
Opportunities located: NJ, NY, CT, MA, PA, NC, GA Summary Responsible for collecting data from clinical trials created for pharmaceuticals, biologics, or devices. Ensures data collected is accurate, groups data properly, solves operational problems, and prepares statistical reports. Primary responsibilities Work with complex computerized records systems and maintain security and integrity. Collect...
Opportunities located in: NY, NJ, PA, MA, NC Summary Responsible for providing medical and clinical insight and guidance through clinical trials for pharmaceuticals. Primary responsibilities Provide medical and clinical guidance to managers before, throughout, and following clinical trials. Maintain consistency of safety assessments. Perform a variety of safety assessments. Serve in cross-function...
Opportunities located in: NY, NJ, PA, MA, NC Summary Responsible for the overall planning and direction of clinical regulatory activities. Develops and implements strategies with the goal of approval of regulatory submission. Primary responsibilities Direct and oversee short-term and long-term planning of regulatory submission initiatives. Interpret corporate policy. Develop and implement strategi...
Who we are: The Cardiovascular Research Foundation, headquartered in New York City, has been dedicated to research and education in the broad subspecialty of interventional cardiology and endovascular medicine for over fifteen years. By establishing the safe use of new technologies and pharmacologic agents, CRF has played a major role in the remarkable advances in survival and quality of life bein...
About Mesoblast: Mesoblast Limited is a world leader in the development of biologic products for the broad field of regenerative medicine. The Company’s proprietary technologies include its highly purified, immunoselected Stro-1/Stro-3 positive Mesenchymal Precursor Cells (MPCs), culture-expanded Mesenchymal Stem Cells (MSCs), Dental Pulp Stem Cells (DPSCs), and expanded Hematopoietic Stem Cells (...
Responsible for the clinical data review of adverse event within clinical database. Assists in SAE reconciliation to resolve discrepancies not limited to coding, and reported term. Collaborates with Data Operations in generating auto generated narrative for clinical data review of Study Directors & for CSR narratives. Responsible for selection and review of appropriate codes of reported terms in c...
Main purpose of the job: To support the Biostatistics team by carrying out and overseeing programming activities of statistical programmers and external vendors (as required), and to ensure timely and accurate programming and validation activities for clinical studies. Contributes to the overall efficiency and best practice running of the Biostatistics group, demonstrating the ability to work effi...
TransPerfect Family of Companies www.transperfect.com Account Executive– Linguistic Validation Summary: We are looking for a successful, competitive, self-motivated individual who has the drive to succeed and will contribute to our next level of growth for the Linguistic Validation department at TransPerfect. The Account Executive position is responsible for actively hunting and developing new bus...
Job Description: Research Technician in Gene Regulation Qualified candidate will perform laboratory tests, prepare specimens and samples in order to produce reliable and precise data to support scientific investigations. Carrying out routine tasks accurately and following strict methodologies to carry out analyses. Recording and interpreting results to present to colleagues and supervisors. Develo...
A leading research institution is seeking Laboratory Assistants with experience in the sanitation of animal cages. Job Duties: · Sanitation and maintenance of animal cages · Familiar with working in a research setting or laboratory · Follow all Standard Operating Procedures · Operate autoclave to sterilize/decontaminate cages · Receive and store materials and supplies...
ESSENTIAL DUTIES Job Description ESSENTIAL DUTIES Provide statistical support, and work closely with other departments in the company for all statistics related activities in clinical trials, such as analyze, report, and interpret the results of clinical trials. GENERAL DESCRIPTION *Responsible for all statistical activities from protocol development to reporting study results. *Use knowledge of t...
Job Description: Manager of Clinical Trial Consultants Description The role of the Reader Manager is to coordinate, manage and support all RadMD readers. This includes sourcing, identifying and providing highly trained, qualified radiologists and other physicians to perform independent image reviews (“blinded reads”) for new drug and medical device clinical trials as well as managing their require...
Become part of a growing team. Collagen Matrix, Inc., located in Oakland, NJ, is a leader in the design and engineering of collagen and mineral-based extracellular matrices for tissue and organ repair and regeneration. The Company currently manufactures collagen and mineral-based finished medical devices in the areas of orthopedic-spine surgery, neurosurgery, oral surgery and wound care. We have a...
Laboratory technician in precious metal assay services laboratory with leader in the chemical industry. Responsibilities: Will be responsible for performing a variety of classical wet chemical and instrumental analyses. Responsible for the measurement of Loss on Ignition/Drying by instrumental methods. Should be familiar with the techniques of instrumental analysis, to include XRay Fluorescence (X...
Woodcliff Lake, 07677
Clinical Study Manager 1 year contract Neuroscience/General Medicine Unit DESCRIPTION This position will support the clinical operations lead in the overall management of clinical studies in Phase II/III including, but not limited to, the development of study start-up materials, clinical supplies, case report forms, contracts and budgets, investigator meetings, and regulatory document filing. The...
Position Summary Provide day-to-day regulatory support for new product development and commercialization projects. Review and approve formulas, raw materials and other product design criteria. Prepare regulatory submissions to health authorities. Maintain up-to-date product registrations, including registration expirations, discontinuances or product changes. Work with Director to determine produc...
A superb opportunity as a Senior Product Manager on flagship brand for one of the best HEM/ONC biotech's out there! I have been engaged to find an "A" player in oncology marketing who also has digital/e marketing experience. There is a need for a top talent to provide strategic and innovative programs to both nurses and patients to fully leverage the lifecycle of this highly valued asset. Cultivat...
YOU CAN WORK FOR A PHARMACEUTICAL COMPANY OR YOU CAN HELP BUILD ONE! Crown Laboratories, Inc. the makers of BLUE LIZARD AUSTRALIAN SUNSCREEN has an opening for a qualified sales professional in Manhattan, NY. Are the Following What You Desire In A Job? Building A Business from the Ground Up A portfolio of quality products that provide benefit and value to patients and providers Customers that are...
Our major pharmaceutical client is currently seeking 2 Clinical Site Monitors to cover sites based in NYC and Northeast Region, as needed. This is a long term, 12 month extendable contract opportunitiy with possibility to convert permanent. Must Have: - Minimum 2 years independent clinical site monitoring experience - Home office within commutable distance to NYC - Must be able to provide professi...
CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Apply Senior Rockstar Research Engineer - eCommerce New York, NY Full-Time $150,000 - $175,000 Apply Apply Senior Rockstar Research Engineer - eCommerce New York, NY Full-Time $150,000 - $175,000 Apply Job Details If you are a Senior Rockstar Research Engineer with experience, please read on! What You Will Be Doing...
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