R & D Jobs in Clifton, New Jersey
187 Clifton, NJ R & D jobs found on Monster.
Currently we have a temporary opening for a Formulations Chemist to support a company located in the Nutley, NJ area. Responsibilities: Formulate OTC drugs including topical analgesics, anti-acne, sunscreen, oral care, antimicrobial, antiperspirants, skin treatment, hair care and general personal care. Develop formulations from concept to finished product based on requests from marketing and other...
Multi national drug discovery company seeks experience performing the following: * Extracting proteins derived from E-coli, Yeast and CHO cells * Purifying Enzymes, MAB’s Cytokines, and Growth Factors * Detailing scale up and document of manufacturing procedures Shall develop purifications procedures from scratch, validate existing procedures and perform viral validation. Excellent opportunity to...
CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Drug Safety Manager Nutley, NJ; Hoboken, NJ Full-Time $100,000 - $130,000 Posted 6/19/2013 Erin Beagle is recruiting for this position. Email your resume to Erin Apply Job Details If you are a Drug Safety Manager, Sr Specialist or Sr Manager who has worked in a pharmaceutical company or CRO in Drug Safety, for at l...
There's quite a distance between wondering and knowing. And for patients waiting for answers to important health questions, it's a road they want to travel as quickly as possible. At Quest Diagnostics Incorporated, we understand urgency. But more than speed, we focus our energies on accuracy. Responsibilities Currently we are seeking a Laboratory Supervisor. As a Laboratory Supervisor, you will pe...
Great opportunity for an experienced Clinical Data Manager! Very stable and fast-growing pharmaceutical company! Long-term contract role! Excellent work environment! Candidate needs to have hands-on experience conducting all DM activities and possess strong project management and excellent interpersonal skills to independently manage a global project. Experience in InForm, Oncology a plus. Indepen...
OVERALL RESPONSIBILITIES:Needed LMS Competencies: Specific to Legacy Plateau Learning Management System: - User management knowledge; managing user needs with respect to assignment and recording of items, and adjusting item completions. - Creating items/Scheduled offerings. - Reporting using stock reports. - SCORM and AICC knowledge - Creation of online content items. Advanced admin track: - Curri...
Canfield Scientific, Inc. is the leading supplier of 2D and 3D photographic equipment, software, and systems for advanced patient imaging serving both physicians and the healthcare industry. Our 3D products are aimed at the following purposes: improve communication between patients and physicians, provide tools for surgical planning, and provide tools for measurement and analysis based on 3D surfa...
Excellent opportunity for experienced Biostatistician! Fast-growing and very stable pharmaceutical company! Excellent work environment! Long-term contract! The client is looking for a self-motivated, PhD or MS statistician with experience in clinical trials who will: • Provide statistical support to protocol; review and provide comment on the study protocol. • Review and approve CCG plan, data cle...
Excellent opportunity for experienced Biostatistician! Very stable, fast-growing pharmaceutical company! Excellent work environment! Long-term contract opportunity! Description of Services Required: • Support clinical trial design and protocol concept sheet development • Develop protocols especially for statistical section • Participate study related activities and provide statistical support such...
Excellent opportunity to work with a fast-growing pharmaceutical company! Great work environment! Long-term contract opportunity! Description of Services Required: · Support clinical trial design and protocol concept sheet development · Develop protocols especially for statistical section · Participate study related activities and provide statistical support such as safety review, interim analyses...
Medical Director Drug Safety & Pharmacovigilance, Oncology: Top 20 Global Pharma Co., Northern NJ Our client is a growing, stable, multi-billion dollar global pharmaceutical company with marketed products in various therapeutic areas. They are looking to hire an experienced Medical Director, Drug Safety to be a key person in leading safety Risk Management Processes, safety assessment activities, i...
. 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 Drug Safety Associate in Northern NJ Description: Ensure timely expedited safety report submissions and SAE filings; draft notification letters to clinical investigators. Ensure SAE files and related tracking systems for complian...
Job Title Central NJ Clinical Research Associate Job Family Clinical Operations PRA Location Regional - North America AutoReqId 12064BR JobDetails JOB SUMMARY: The Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating pro...
Statistician&SAS(remote),LSH–Oracle Clinical,Medical Writer,Clinical data manager,Biomarker Trial He
TechData is hiring Biostatistician (some can telecommute), SAS Programmer (Some can be telecommute), Sr. Clinical data manager, Sr. Medical Writer,Life Sciences Hub (LSH) Consultant and Oracle Clinical for Global Librarian/Modeler, Biomarker Trial head for our pharmaceutical clients in Northern NJ. Please see below requirements and send your inquiry and resume to: dan.chen@techdataservice.com or r...
Statistical Programmer with 5+ years experience supporting clinical trials in the Pharmaceutical industry. Strong drug development background and experience programming all phases of clinical trials, with NDA/submission experience. MS degree strongly preferred, in statistics/biostatistics. Experience leading statistical programming activities for drug projects and interacting with clinical project...
Company Confidential
Newark, NJ, 07105
Junior Application Chemist This position will play an important role in increasing sales of Cardolite epoxy products among coating and adhesive manufacturers by developing performance data for new formulations and markets, supporting customer and marketing projects, helping troubleshoot and solve technical issues, and writing product test bulletins. Essential Functions: · Conduct laboratory testin...
This position reports into Head of Global Sourcing Area and works within Procurement across legal entities and national boundaries with a strong focus on procurement strategy and service delivery. This position would provide contract support within a therapeutic or division specialty. This position will also support the identification, selection, and management of suppliers and contracts across th...
Position Responsibilities: Participate in all aspects of clinical development and study management under the direction of the Director. Participate in overseeing the activities of Clinical Research Organizations (CROs) and other third party vendors in the conduct and management of the Phase 1 clinical trials. Closely monitor and track progress of clinical trials and oversee contract clinical resea...
Position Responsibilities: · Write routine cover submission cover letters and forms · Work with Octagon to ensure high quality and timely submission · Archive regulatory submissions and correspondence according to SOP · Track submission components with internal and external authors · Assist with IND and BLA related activities · Maintain regulatory tracking documents · Ensure all documents are BARD...
Associate Chemist/Laboratory Technician Responsibilities · General laboratory duties in precious metal assay services laboratory · Responsible for standard operation, as well as analytical testing · Perform accurate and timely measurements using ICP, voltammetry, XRF, and other laboratory equipment · Capable of working in a fast-paced analytical environment · Must be able to work independently wit...
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©2013 Monster - All Rights Reserved U.S. Patents No. 5,832,497; 7,599,930 B1; 7,827,125 and 7,836,060 MWW - Looking for Monster Cable? - V: 2013.5.0.223-223