R & D Jobs in Clifton, New Jersey - Page 2

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

Jobs 21 to 40 of 205
PRINCIPAL SDTM PROGRAMMER *This remote opportunity is open to any US home-office location. Theorem Clinical Research is currently searching for experienced SDTM Programmers. In this role, the SDTM Programmer will be responsible for mapping entire studies in accordance with SDTM guidelines, as well as performing Quality Control checks. RESPONSIBILITIES: Create SAS datasets of clinical data from cli...
Job Responsibilities: · Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites for GCP compliance according to PharmaNet SOPs and/or client guidelines · Generate study specific documentation including monitoring trip reports, telephone contact reports, site correspondence and expense reports · Recruit investigators for participation in clinical trials · Conduct projec...
Job Title - Healthcare Policy and Informatics Specialist Type - Permanent Location - Fort Lee, NJ Salary - DOE Our clients Quality Division is seeking a Healthcare Policy and Informatics Specialist with experience in navigating the changing healthcare environment regarding the various government and commercial quality incentive programs. The successful candidate will have a demonstrated track reco...
Position: Senior Decision Analytics Consultant “Emphasis is on end product delivery of analysis and guiding junior staff” Role: · Contribute and guide the team on structural analysis of the project Contribute and guide the team on insights from conclusions of analysis that integrate with initial hypothesis and business objective · Independently address complex problems · Participate in design of m...
We have a Contract opportunity with a prominent client for a Biochemist in Franklin Lakes, NJ. Qualifications: A Ph.D. in cell biology, molecular biology, or related field with a minimum of 5 years of laboratory experience is required. A focus in the area of immunology and/or cell therapy is desired. Cell analysis skill sets such as flow cytometry and microscopy are required. Experience with metab...
Candidates cannot begin an assignment without successful completion of drug and background screenings. 1 Year Contract Assignment $35.00 Hourly Qualifications: A Ph.D. in cell biology, molecular biology, or related field with a minimum of 5 years of laboratory experience is required. A focus in the area of immunology and/or cell therapy is desired. Previous Post-Doc experience is not required. Cel...
7+ years of PRO-E experience designing disposable medical instrumentation - Design of plastic parts (DFM, Tolerance Stacks, GDT) - Design of mechanisms (gears, slides, actuators) - Knowledge of plastics - Working knowledge of the injection molding process...
NEW Position- Sr Manager Field Operations Experience: 3 - 5 years of pharmaceutical sales operations Compensation: $120,000.00 - $145,000.00 Job Description: The Senior Manager of Field Operations is responsible for the development, analysis, and implementation of sales force strategy and tactics to include resource optimization, field force size and structure, targeting, alignments, personnel pla...
*BA/BS or advanced degree required! 3 years of experience required!* Duties: The team is looking for highly motivated and pleasant individuals with previous experience a clinical trial site in a global pharma company or those with experience in conducting a global study. We have a strong preference for those with a strong scientific or clinical background (i.e., oncology nurse, pharmacists, etc) a...
Hello, My name is Bryson Jackson and I represent The Fountain Group. We are a national staffing firm and are currently seeking a Desktop Publisher (s) for a prominent client of ours. This position is located in East Hanover, NJ. Details for the positions are as follows: Job Description: LONG TERM CONTRACT!!!! FORTUNE 500 CLIENT!!!! Duties Responsible for publishing and managing QC for high quality...
Desktop Publisher – 6 month contract Responsible for publishing and managing QC for high quality scientific documentation (e.g. study reports) for submission to regulatory authorities in support of marketing applications. Preparation of high quality scientific documentation and submission documents in accordance with the timelines specified by Novartis Institutes for BioMedical Research (NIBR) and...
Clinical Research Scientist – 6 month contract, East Hanover, NJ The team is looking for highly motivated and pleasant individuals with previous experience a clinical trial site in a global pharma company or those with experience in conducting a global study. We have a strong preference for those with a strong scientific or clinical background (i.e., oncology nurse, pharmacists, etc) and those wit...
The Fountain Group has an IMMEDIATE opening for a Clinical Research Scientist in east Hanover, NJ. Qualified candidates should submit an updated resume along with contact information to be considered. Overview The team is looking for highly motivated and pleasant individual with previous experience at a clinical trial site in a global pharma company or those with experience in conducting a global...
Clinical Research Manager II – 6 month contract Support US efforts in the planning, execution and reporting of US Clinical Data and Medical Affairs (CDMA) clinical trials in Oncology: Implementation of clinical trials in the United States (safety, data consistency, trial timelines, budget, resources, eligibility and enrollment), within a cross functional team and with oversight from the Associate...
Biostatistician III – 6 month contract Designing clinical studies. Writing and reviewing statistical sections and other relevant parts of study synopses and protocols. Support study start up activities. Develop RAP, program TLFs, preparation for database lock, dry run and CSR activities. Review CRF, DB spec, VAP. Support analyses as required for decision making at project level. Support analyses a...
Hello, My name is Donald and I represent The Fountain Group. We are a national staffing firm and are currently seeking a Biostatistician III for a prominent client of ours. This position is located in East Hanover, NJ. Details for the positions are as follows: Job Description: Designing clinical studies. Writing and reviewing statistical sections and other relevant parts of study synopses and prot...
We have a Contract opportunity with a prominent client for a Managed Care Contract Analyst III in East Hanover, NJ. Duties: Accurately enter contracts and maintain membership for various market segments into Model N and SAP, to ensure accurate data availability to allow for flexible and meaningful management reporting, chargeback processing and rebate adjudication. Conduct peer review sessions. Po...
TechData is looking for Biostatistician (Contract/permanent, or remote), SAS Programmer/Statistical Programmer (Some can be telecommuting), Task Based Clinical Data Coordinator/Clinical Data Manager, CRS (Clinical Research Scientist, Clinical Scientist), Clinical Safety Scientist/Drug Safety for our pharmaceutical clients in Northern and Central NJ. Please see below requirements and send your resu...
Expert Clinical Manager III – 5 month contract Responsible for all operational aspects of 1 or more Office of Generic Drugs (OGD) clinical trial(s) under the leadership of Clinical Trial Head (CTH). Support all scientific aspects of clinical trial(s) as assigned. Responsible for program level activities as assigned. Ensure all operational trial deliverables are met according to timelines, budget,...
Minimum Requirements: Prior experience with Implementation of clinical trials in the United States safety, data consistency, trial timelines, budget, resources, eligibility and enrollment. Education: Bachelor Degree required Job Description: Support US efforts in the planning, execution and reporting of USCDMA clinical trials in Oncology. Implementation of clinical trials in the United States (saf...
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