Biotech Jobs in Bridgewater, New Jersey

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203 Bridgewater, NJ Biotech jobs found on Monster.

Jobs 1 to 20 of 100
Our client is a one of the world’s largest and most respected Pharmaceutical companies, headquartered in New York City, devoted to discovering new medicines, new technologies and new ways to manage health for people and their valued animals. Their purpose is helping people live longer, healthier, happier lives- adding both years to life, and life to years. They have a consistent need for Health Ca...
PerkinElmer is a global technology leader driving growth and initiative in the Environmental and Human Health Science markets. The company is a leading force in the development, production, marketing, servicing, and supporting of laboratory instrumentation and ancillary services throughout the world. Why OneSource? OneSource is a multi vendor service organization that allows our business partners...
Responsibilities: Independently perform statistical programming to support statistical analysis of the clinical data and submission to regulatory agencies. Supervise the activities of specialists in statistical programming. Generate or quality check data listings, tables and figures (TFL) from clinical data, using SAS or other statistical software. Review clinical protocols, SAP, TFL shells, and c...
Duties: To perform tasks under the guidance of project lead or CMS departmental principals on analytic design and statistical analytic planning coordinate real world database management, and data warehouse construction or maintenance develop documentations of analytic plans, prepare for statistical concept communications and be able to advise on analytic strategies and recommend methodological sol...
Sound Advice is a boutique consulting services firm headquartered in New York with a national presence. We have a reputation for quality and excellence in the Pharmaceutical and Life Sciences space. Sound Advice has a long term strategic partnership with one of the world’s largest and most respected Pharmaceutical companies, headquartered in New York City. We have been engaged to provide consultan...
This position is responsible for ensuring compliance with Federal regulations pertaining to GMP/QSR, and ISO13485 and associated regulatory agencies through effective management of the drug and device complaints process This position will be responsible for directing personnel and maintaining all activities associated with customer complaints. Working closely with the Customer Service and Field se...
Please review position description carefully - True Job Title - CEP Operations Specialist Perform operational activities to support the CEP inventory; ensure timely and accurate maintenance of the inventory database . Generate timely and accurate notifications to CEP owners and others involved in CEP processes . Support metrics and information gathering related to the quality of the CEP inventory...
Manager, Clinical Study Mindbank Consulting Group has an immediate need for a Manager, Clinical Study with a premier Pharmaceutical Company. This is a full time permanent position with outstanding benefits and a great work/life balance! The Manager, Clinical Study will be responsible for all study management aspects of a global clinical study including but not limited to the tasks listed below. Fo...
Mindbank Consulting Group has an immediate need for a Manager, Clinical Study with a premier Pharmaceutical Company. This is a full time permanent position with outstanding benefits and a great work/life balance! The Manager, Clinical Study will be responsible for all study management aspects of a global clinical study including but not limited to the tasks listed below. For all of the global stud...
. Adecco Engineering and Technical, a division of the world leader in the recruitment of Scientific and engineering professionals, has an immediate opening for a contract Data Management SAS Programmer in Northern NJ Description: Responsible for the role which includes acquisition, integration, and delivery of Clinical Study Data. Documentation and peer review of deliverables. Assist with the role...
Mindbank Consulting Group currently has an urgent and immediate need for a Manager of Statistical Programming to work for one of our prestigious clients. The Manager of Statistical Programming will provide specialized knowledge and leadership to carry out statistical programming activities in support of studies. Manager of Statistical Programming Responsibilities: · Planning, organizing, and manag...
JOB ID: PB1078 JOB TITLE: Principle Clinical Services Specialist CONTACT: juliann.cruikshank@mindbank.com LOCATION: Bridgewater, NJ START DATE: Immediate JOB TYPE: Permanent Position SALARY: $ 103,000K plus an 11% bonus annually Job Description Overview: MINDBANK Consulting Group has an immediate need for a Principal Clinical Services Specialist for a highly reputable Pharmaceutical Company. Respo...
TechData is looking for Outcome research statistician, Biostatistician (some can be telecommuting), SAS Programmer/Statistical Programmer (Some can be telecommuting), Sr. Clinical Data Manager, Drug Safety Specialist, Medical Writers for our pharmaceutical clients in Central NJ. Please see below requirements and send your resume to: dan.chen@techdataservice.com or recruiting@techdataservice.com. T...
. Adecco Engineering and Technical, a division of the world leader in the recruitment of Scientific and engineering professionals, has an immediate opening for a contract Data Management SAS Programmer in Northern NJ Description: Responsible for the role which includes acquisition, integration, and delivery of Clinical Study Data. Documentation and peer review of deliverables. Assist with the role...
Provide statistical programming expertise in SAS for the production of analyses, tabulations, graphics, and listings from clinical trial data. Key responsibilities and skills include, but are not limited to, the following: Contribute to the preparation of analysis plans. Prepare, document and test required programs and procedure data displays in an efficient manner for inclusion in integrated clin...
DIRECTOR OF LICENSING - PHARMACEUTICAL TECHNOLOGY JOB SUMMARY: Responsible for identifying, evaluating, structuring, negotiating and closing technology and product licensing deals in support of Aptalis’s Pharmaceutical Technology (PT) business. The Director of Licensing will build relationships with potential PT partners in the pharmaceutical industry and will identify opportunities for high value...
. Adecco Engineering and Technical, a division of the world leader in the recruitment of Scientific and engineering professionals, has an immediate opening for a contract Clinical Study Manager in Bridgewater NJ Description: The Senior Clinical Manager/Clinical Manager will ensure that clinical strategies are translated into operational plans and executed in line with clinical development plans. I...
JOB SUMMARY: Increasing innovation in R&D is one of the major thrusts under the transformed R&D organization. Sanofi-aventis believes that the majority of early innovation in healthcare would be generated outside of pharma companies. Consequently, we need to be well equipped to partner with external innovators. The PSI (Prospective & Strategic Initiative) organization is the main partnering arm of...
Responsibilities Clinical Planning Collaborate with the business unit geographical regions, Discovery, Program Phase Medicine, and Clinical Pharmacology in the development and maintenance of a Draft Launch Label and Value Proposition that addresses key customer needs (patient, provider, and payer); the product lifecycle plan, clinical strategies, development plans and study protocol design. Contri...
In more than 100 countries, the people of Ashland Inc. (NYSE: ASH) provide the specialty chemicals, technologies and insights to help customers create new and improved products for today and sustainable solutions for tomorrow. Our chemistry is at work every day in a wide variety of markets and applications, including architectural coatings, automotive, construction, energy, food and beverage, pers...
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