R & D Jobs in Union, New Jersey

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205 Union, NJ R & D jobs found on Monster.

Jobs 1 to 20 of 205
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...
· 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...
Hays is currently recruiting for a Project Manager for our global pharmaceutical client located in Northern NJ. This hands-on, process driven Project Manager position is a 6 month contract job. This position is an excellent opportunity to leverage your Drug Development and Regulatory Filing experience in a tangible project-based setting. This position will be responsible for hands-on daily projec...
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...
Company Confidential Newark, NJ, 07101
Currently seeking dynamic sales entrepreneurs for a unique career opportunity in compounding pharmaceutical sales in the greater Newark area. Requirements · 5-7 years pharmaceutical sales experience · Established relationships with specialists in interventional pain management and/or: orthopedics, rheumatology, neurology, endocrinology, podiatry, oncology and primary care physicians. Preferenc...
Worldwide Clinical Trials is a therapeutically focused global CRO that provides full-service drug development services to the pharmaceutical and biotechnology industries. As one of the most innovative and scientifically-driven contract research organizations, we offer exceptionally strong clinical trial methodology integrated with an effective global operations network. We are currently seeking hi...
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...
Early Clinical Development Specialist - III Must have: - BS degree (will not consider non-degreed) - Direct clinical experience (e.g. nursing) or experience conducting Phase I clinical research in the pharmaceutical industry - Phase I experience with direct tasks of regulatory document authoring (protocols, clinical study reports, IND updates), project management/oversight for Phase I studies,...
Job Purpose: Maintains product quality by conducting microbiologic tests; communicating results. Duties: * Organizes work by confirming product specifications. * Maintains clean and safe work environment by maintaining aseptic methods and protocols; following standards and procedures; complying with legal regulations. * Prepares cultures by obtaining in-process and finished product samples. ...
Industry: Pharmaceutical Must have: - BS Life Sciences/Engineering - Experience supporting clinical trials/programs - Experience with Microsoft Project - Experience with Clinical Trial Management Systems such as Spectrum or Impact Responsibilities: · The Clinical Project Specialist will be responsible for supporting and managing the Early Stage Clinical Development functional area planning ...
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...
Requirements: -Educated to degree level (biological science, pharmacy, or other health-related discipline preferred), equivalent nursing qualification or other equivalent experience (degree is not required) -Min 5 yrs experience within biotech/CRO or smaller company (can’t just have big pharma exp), would consider experience over degree but depends on background, (high exp working in house, they...
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...
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...

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