Bridgewater
R & D Jobs in Bridgewater, New Jersey
179 Bridgewater, NJ R & D jobs found on Monster.
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...
Validation Manager · Project manage client’s projects, including but not limited to development of project plans, manage client assigned timelines and budgets. · Responsible For Quality Assurance process review and documentation · Develop requirement documents, test scripts, quality plan, gap analysis, gap analysis and test remediation · Perform code reviews · Writing quality system oriented SOPs....
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...
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...
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...
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...
Remote Contract Medical Writer Location: Home-based (company office located in Holliston, MA) Job Type: Full-Time Duration: 3-6 months contract (possible contract extension) Compensation: Open to discussion Summary of Job Responsibilities: · Write Patient Narratives for phase III oncology trials · Adhere to sponsor’s template and format for all narratives · Meets critical project deadlines and sub...
Responsibilities Candidate, as a member of Biostatistics and Programming Department, will provide statistical supports for Phase 2/3 clinical studies and/or perform statistical methodology research. The candidate will closely collaborate with project teams consisting of clinicians, project managers, clinical trial managers, data management and other functions. Activities include preparing study pr...
Job Summary: The purpose of this job is to create, without supervision, any type of clinical regulatory document (e.g., protocol, CSR, CIB, clinical sections of IMPD and CTD) according to company guidelines and international governmental regulations and to present clinical data objectively in a clear, concise format. This position is for an independent, proactive, experienced medical writer with d...
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...
Johnson & Johnson companies are equal opportunity employers. STAFF SCIENTIST ANALYTICAL DEV-6680130424 Description Cordis Corporation, a member of Johnson & Johnson&'s Family of Companies, is recruiting for a Staff Scientist, located in Somerville, NJ. Cordis is a recognized leader in providing physicians with breakthrough treatment solutions for peripheral vascular disease, a leader in circulator...
COMPANY PROFILE Sound Advice is a boutique consulting services firm headquartered in New York with a national presence and 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, dedicated to supporting a vari...
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...
Global Pharmaceutical company is seeking a Compliance and Analytics consultant for a contract position for a minimum one year contract. Analyst will provide site perspectives to the Quality Safety Team Leads with adherence to safety, regulatory, and project timelines, bridges partnership with customers to support “in line” quality ownership and participates in the development of efficient tools an...
. Adecco Engineering and Technical, a division of the world leader in the recruitment of scientific and engineering professionals, has an immediate opening for a SAS Programmer with Pharmaceutical and Clinical Trials experience for a contract position in Bridgewater, NJ RESPONSIBILITIES: Knowledge of FDA regulations (21 CFR part 11) and guidelines in new drug development and application process re...
. Adecco Engineering and Technical, a division of the world leader in the recruitment of scientific and engineering professionals, has an immediate opening for a SAS Programmer with Pharmaceutical and Clinical Trials experience for a contract position in Bridgewater, NJ RESPONSIBILITIES: Knowledge of FDA regulations (21 CFR part 11) and guidelines in new drug development and application process re...
Director / Senior Manager Regulatory Affairs Post Marketing Basic Responsibilities: · Represent Regulatory Affairs on Promotional Review Committee · Act as the primary point of contact with OPDP · Handle BLA/NDA post approval FDA responsibilities · Oversee Clinical from a Quality perspective Job Requirements: Knowledge and Skills Required: · Minimum 5 years of regulatory affairs post marketing exp...
Associate Director Regulatory Affairs Advertising and Promotions My client recently had one of their two programs approved in January 2013! They have doubled their headcount since in the last ten years to over 300 employees. Their youthful energetic leadership team is seeking an Associate Director of Regulatory Affairs Ad/Promo to help them reach their solid vision! As the Associate Director you w...
My client has been one of the top 20 pharmaceutical companies for the last 10 years. With a rich pipeline of CNS, Oncology, Immunology and GI-focused medicine, this organization will continue on their steady growth path. As the company prepares for new drugs to hit the market, they are expanding their Product Safety department. Location: North New Jersey Job Responsibilities: · Provides medical ex...
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