R & D Jobs in Summit, New Jersey

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

Jobs 1 to 20 of 221
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...
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...
Currently we have a temporary opening for Lab Technician to support a company located in the East Hanover, NJ area.   Responsibilities: Sets up, operates and maintains laboratory instruments, monitors experiments, makes observations, calculates and records results, and often develops conclusions. Individual is familiar with basic scientific principles and has had some laboratory experience. C...
Support study data management and data cleaning process on an ongoing basis, applying study specific documents and conventions. Identify and issue queries, incorporate query replies, track query status and apply permissible clarifications using the EDC (e.g., RAVE) and related systems (e.g., SAS, jReview, etc.). Assist in documentation gathering and archiving. Minimum 3 years as a Study Data Mang...
Job ID: 4294 Position Description: Company Overview At EngageCE, a division of PDI, Inc., we believe instilling positive behavior within the practice is the cornerstone of providing optimal patient care. Many practices face challenges and old habits that impact their ability to follow care recommendations, which can negatively impact patient outcomes due to: • Difficulty establishing and maint...
Our client is a growing CRO offering an outstanding opportunity to join their organization and play an integral part of their departmental growth. This position provides leadership and guidance as the statistical expert to ensure projects are optimally strategized, correctly designed, properly analyzed and clearly presented to support new product development, domestic and international regulatory...
Currently we have an opening for Pilot Plant Technician to support a company located in the Clinton, NJ area. Responsibilities: Operate multiple pilot plants simultaneously using Honeywell and/or Labview/Bridgeview process control computing systems. Run programs per detailed instructions from researchers Monitor unit performance and diagnose any deviations vs. desired program Become familiar ...
· High school diploma or general education degree (GED) is required; and one year related experience in QA Inspection; or combination of education and experience. · Ability to read and comprehend simple instructions, short correspondence, and memos in English. · Ability to speak effectively in English in one on one or small groups. · Ability to add, subtract, multiply, and divide in all units o...
Senior Manager Regulatory Affairs Location: Iselin, NJ Duration: 6 months Requirements: -At least a Bachelor’s degree in Life Sciences (preferably a Master’s degree) -Minimum of 10 years general Regulatory industry experience, with the preponderance of experience being in the area of Regulatory advertising and promotion review. Responsibilities: Promotional material (75%): -Collaborate wit...
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...
Seeking a Data Analysis Specialist for a consulting position at a major pharmaceutical client in East Hanover, NJ. Job Purpose: Prepare trending reports from raw data Excel source documents as per applicable SOP’s and template. Education: Typically requires a B.S. or equivalent in education and experience in pharmaceutical industry. Experience: Basic understanding of statistical analysis In...
Are you looking for a Clinical Research position with a large pharmaceutical company? TechData Service has multiple contract positions open with many top pharmaceutical companies for job titles including Executive Assistant, Regulatory Document Specialist, Business Analyst, Sales Operations Specialist, CRA Monitor, Scientist IV, Pharmacovigilence Specialist, Medical Writer, Biostatistician and SA...
Are you looking for a Clinical Research position with a large pharmaceutical company? TechData Service has multiple positions open with many top pharmaceutical companies for positions including Project Manager with quality systems experience, Drug Safety Coordinator, Pharmacovigilence Scientist, Clinical Operations Manager/Project Manager, Scientist, Medical Information Specialist, CRA Monitor, C...
Job Number: 423062 Sr. Clinical Research Scientist 4028452 Duties: Scientific and operational lead for execution of the US clinical trials within budget and in compliance with company processes and regulatory requirements, with a strong emphasis on US customers and Health Authorities' requirements. 1. Acts as US trial leader in the management and conduct of CAR T cell Therapy clinical trials w...
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...
TechData is looking for Regulatory Specialist, Biostatistician (Some remote), SAS Programmer/Statistical Programmer (Some can be telecommuting), Clinical Research Scientist, Clinical Research Physician, Drug Safety Specialist, Safety Trial Manager, Medical Affairs Contract Manager/Outsourcing manager, Sr. Clinical Data Manager, for our pharmaceutical clients in Central NJ and Northern NJ. Please s...
Submissions Coordinator Duration: 5-months Berkeley Heights, NJ Responsibilities: Provides support including, but not limited to, the following for the Global Regulatory Operations team: - Archiving of Health Authority correspondences, MS Word and PDF processing, and document and record management. - Provide MS Word processing support for preparation of regulatory submission documentation. ...
Quality Assurance Specialist Location: Berkeley Heights NJ Duration: 6 months Requirements: -BS in the Sciences or Pharmaceutical related field is preferred with 2-4 years relevant QA experience. -Alternatively, 2 years of higher education with 4 years relevant QA experience may be acceptable. -Good computer skills and working knowledge of common business software -Good knowledge of GMP req...
Great opportunity to join a leading, global medical device technology firm. This position will collaborate with Divisional and Global Regulatory staff to execute the company’s regulatory strategies ensuring successful approval of international product registrations and renewals. Primary Job responsibilities: · Effectively deal with regulatory issues across business units and geographic location...
Leading pharma client seeks a Sr. Clinical Research Scientist for a 6 month contract. Scientific and operational lead for execution of the US clinical trials within budget and in compliance with processes and regulatory requirements, with a strong emphasis on US customers and Health Authorities' requirements. 1. Acts as US trial leader in the management and conduct of CAR T cell Therapy clinical...

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