R & D Jobs in Springfield, New Jersey

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242 Springfield, NJ R & D jobs found on Monster.

Jobs 1 to 20 of 242
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...
· 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...
Outstanding CDM opportunity available with a growing clinical research organization in the Northern New Jersey area. A positive work environment and recognition of the importance of work life balance has led to employee satisfaction and company success. A competitive salary and comprehensive benefits package are offered. Job responsibilities: The Sr. / Clinical Data Manager leads data management...
Reporting to the Vice President of Manufacturing, the R &D Manager will serve as Novel’s internal expert resource in driving custom manufacturing growth. Through a detailed knowledge base of natural ingredient properties, manufacturing applications and end product flow, granulation and other characteristics, the R&D Manager will lead and create new product samples that can be scaled for large volu...
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...
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...
Company Confidential Summit, NJ, 07901
Exciting Data Management position with excellent potential. We are eagerly reviewing new resumes. Please submit if you feel qualified with the below skills. Responsibilities will include, but are not limited to: 1. Functional proficiencies: • Reviews synopsis/protocol and attends Synopsis Review Committee (SRC) meetings • Leads DM study start-up and maintenance activities - CRF design/edit che...
CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Apply Chief Data Scientist Florham Park, NJ Full-Time $120,000 - $175,000 Apply Apply Chief Data Scientist Florham Park, NJ Full-Time $120,000 - $175,000 Apply Job Details We are a leading data analytics firm within one specific resource extraction vertical- a small company, but with a big footprint o...
Responsible for the management of outsourced contract manufacturing organizations (CMOs) involved in the production of APIs and finished dosage forms for the Company during late-stage development and commercialization phases of product life-cycle. The project manager will have responsibility for tracking project contracts, budgets, timelines and deliverables. The project manager will also provide ...
Manage projects/engagements delivering health economics/outcomes research (HEOR) modeling and analytic solutions. Familiarity with the application of analytics to HEOR problems such as: • Cost-effectiveness model design, including Markov and discrete event simulation (DES) models. • Integration of data from multiple sources, such as clinical trials, claims databases, and literature. • Biostatis...
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...
Our client, a reputable pharmaceutical company, is currently seeking a Sr. Scientist - Clinical Pharmacology. Successful candidates will: Cross project Clinical Pharmacology support for late stage clinical programs. Contribute to the design and coordination of pharmacokinetic / DMPK related elements for clinical projects. Identify potential project hurdles, suggest solutions and establish cont...
Seeking a Product Complaint Specialist for a consulting position at a major pharmaceutical client in East Hanover, NJ 07936. Responsible for the handling and oversight of medical and technical, critical and non-critical customer complaints under company complaint policies and procedures, while assuring compliance with federal regulations. · Supports the entry and maintenance of customer complain...
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...
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...
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...
Job Number: 423225 SAS Programmer Responsibilities will include, but are not limited to, the following: 1. Provide programming input to CRF, SAP, analysis file specifications, and tables, figures, and listings (TFLs) shells. 2. Write SAS programs to generate derived analysis datasets, perform analysis, and TFLs. 3. Perform ad hoc flexible and rapid programming arising from questions generated f...

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