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R & D Jobs in Mahwah, New Jersey

307 jobs

PwC/LoS Overview: 60169043373 Job Description When our pets inspire us every day, it's important to make sure they have everything they need, right when they need it. As an Assistant Store Leader, youll support the Store Leader in leading and inspiring associates and help provide an outstanding experience for our pet parents. Youll direct merchandising and inventory standards within the store, ...
An award winning pharmaceutical company is looking to expand their R&D group in the Americas across clinical, regulatory, quality and biometrics. They are looking for two Senior Global Clinical Project Managers to lead cross functional global teams. As this organization continues to grow there will be opportunity to grow with them, taking on more responsibility and leading both internal and extern...
Must have: Minimum Bachelor’s Degree Chemistry Minimum 5-10 years of experience in pharmaceutical industry with emphasis on regulatory activities Strong working knowledge of FDA, ICH and EU guidelines related to regulatory topics Experience with injectable products as well as labeling requirements and familiarity with eCTD viewers such as eCTD Express (CSC), ViewPoint (Accenture) and ISI ToolB...
Hi There! New Contract Opportunity!! MANAGER LEVEL BIOSTATISICIAN Major Pharmaceutical Company 12 Months Contract Woodcliff Lake NJ MANAGER LEVEL BIOSTATISICIAN Responsibilities: - Work with the clinical study team on study design, development and/or review of clinical study protocols. - Contribute to clinical trial design, protocol concept sheet and protocol development - Participate st...
Hello New Contract Opportunity Biostat programmer Major Pharmaceutical Company 6 Month Contract North New Jersey Biostat programmer - *Must have Submission and Dataset Experience Neuroscience General Medicine Responsibilities: Providing statistical programming and validation support for clinical study reports, overseeing programming activities by external vendors (e.g., CROs) when necessa...
US Tech Solutions is seeking a “Sr. SAS Programmer Analyst” for a 12 Months Contract position with a client in Woodcliff Lake, New Jersey. Responsibilities: Perform SAS programming to provide data review complex listings/reports to support Data Management function for Oncology trials. Focus on candidate with experience in writing SAS tools and developing generic SAS programs for clinical studie...
US Tech Solutions is seeking a “Sr. SAS Programmer Analyst (JReview/listings)” for a 12 Months Contract position with a client in Woodcliff Lake, New Jersey. Responsibilities: Perform SAS programming to provide data review complex listings/reports to support Data Management, Medical Coding, and other areas of Clinical functions for Oncology trials. Develop programs & graphs in JReview for easi...
US Tech Solutions is seeking a “Senior SAS Programmer Analyst” for a 12 Months Contract position with a client in Woodcliff Lake, New Jersey. Responsibilities: Responsible for SDTM data creation and delivery for oncology studies. Prepare SDTM Mapping specification following company standards. Create or participate in SDTM annotation for CRFs/eCRFs for oncology trials. Develop programs to crea...
US Tech Solutions is seeking a “Biostat Programmer” for a 12 Months Contract position with a client in Woodcliff Lake, New Jersey. Responsibilities: Providing statistical programming and validation support for clinical study reports, overseeing programming activities by external vendors (e.g., CROs) when necessary and coordinating programming activities among the study programmers to achieve tim...
US Tech Solutions is seeking a “Senior Clinical Data Manager” for a 6 Months Contract (with possible extension) position with a client in Woodcliff Lake, New Jersey. Responsibilities: l Project Data Management level. l Perform DM activities for in-house and outsourced trials: protocol review, CRF development, database set up activities, data validation process (including manual data review of l...
Job Title: Medical Writer Location: Woodcliff Lake NJ Duration: 1 Year Job Summary Work directly with clinical study teams, the Oncology medical writing teams, regulatory affairs personnel, and the publishing group in the preparation of scientifically valid regulatory documents. Responsibilities include preparation of regulatory documents in accordance with the ICH guidelines, international r...
Eisai Inc. was established in 1995 and began marketing its first product in the United States in 1997. Since then we have rapidly grown to become a fully integrated pharmaceutical business. Eisai’s areas of commercial focus include neurology, gastrointestinal disorders and oncology/critical care. The company serves as the U.S. pharmaceutical operation of Eisai Co., Ltd., a research-based human hea...
Company Confidential
ORGANIC CHEMIST POSITION General Description: (essential job functions and responsibilities) Perform Organic and nutrient analysis using Gas Chromatography and Gas Chromatography/Mass Spectrophotometer and Ion Chromatography instrumentation to meet common goals for WQ, SDWA, CWA, NJPDES Permits and residual analysis. Computer LIMs work and record keeping for input and transfer of analytical dat...
Our client is currently seeking a Analytical Researcher-summer intern. This position is for a summer intern: Objective The successful candidate will undertake an assessment of polymer characterization using Advanced Polymer Chromatography and Supercritical Fluid Chromatography. The initial assignment will be to determine solubility characteristics of various polymers to evaluate their compatibil...
Job Description : Temporary / Contract (3+ month assignment) for Regulatory Affairs Associate to review regulatory submission documentation for U.S. and overseas applications (IND, NDA, BLA, CTA, MAA). Generate, review, and approve regulatory documents in cross functional team environment. Position is with a growing Northern NJ pharmaceutical company. Provide regulatory support and guidance for...
Description: We’re fast becoming the nation’s largest employer of Nurse Practitioners; offering a superior professional environment and incredible opportunities to make a difference in the lives of patients. This growth is not only a testament to our model’s success but the efforts, care, and commitment of our Nurse Practitioners. Serving millions of Medicare and Medicaid patients, Optum is the ...
Description: We’re fast becoming the nation’s largest employer of Nurse Practitioners; offering a superior professional environment and incredible opportunities to make a difference in the lives of patients. This growth is not only a testament to our model’s success but the efforts, care, and commitment of our Nurse Practitioners.Serving millions of Medicare and Medicaid patients, Optum is the na...
Everest Clinical Research ("Everest") is a contract research organization providing statistical, data management, statistical programming, medical writing, subject randomization and drug supply management, regulatory submission, and clinical trial management to pharmaceutical, biotechnology, and medical device companies. We serve some of the best-known companies worldwide, and work with many of t...
Opportunity for a Product Manager to represent CRO specializing in high-throughput drug screening and combination compound testing for cancer therapies. This Manager will design GTM (Go-To-Market) Plans and act as liaison between R&D, Operations, Marketing, Product Development, and Sales. He or she will coordinate a complete marketing-mix for cancer drug development assay services from initial mar...
Seeking individual with experience designing, developing, and approving clinical strategies leading to the commercialization of biologic therapeutics treating infectious diseases. Shall: *** Design clinical strategies for multiple drugs in various stages from first-in-human to Phase III. *** Oversee clinical development programs for novel vaccines, mAb drugs, enzybiotics, biosimilars, etc. ***...