Skip to main content
X

Get jobs by email for this search

By continuing you agree to Monster's Privacy policy, Terms of use and use of cookies.

R & D Jobs in Westwood, New Jersey

949 jobs

Overview Our Discovery Research team has an opening for a Scientist 1 in vivo biologist, reporting to the Director of the In Vivo group. The qualified individual will have a record of high quality contributions to preclinical drug discovery for CNS disorders exemplified by impact on decisions in discovery programs, as well as publications in peer-reviewed journals and presentations at scientific ...
I have a contract for a Clinical Study Manager (Clinical Study Manager/Clinical Project Manager/CPM) on a long term basis for several major biopharmaceutical firms. The Clinical Study manager will be required to have a minimum 5 years experience working as a Clinical Study Manager in a Pharmaceutical setting. This is a great opportunity to further your career as either a Clinical Study Manager or...
Job Description: Prominent global pharmaceutical company is seeking a BIOSTATISTICIAN, SR to work in Jersey City, NJ. This is a six to twelve (06-12) month CONTRACT assignment, with the possibility of extension/temp-to-hire. Max pay is $70.00/hour. Summary: This position will provide sound statistical support in the design and analysis of clinical studies, including study protocol development...
ENTRY LEVEL SCIENTIST WITH PHARMACEUTICAL INDUSTRY EXPERIENCE REQUIREMENT #16-01105 RECRUITER: ANITA JORDAN JOB LOCATION: JERSEY CITY, NJ JULY 14, 2016 *** CANDIDATES MUST BE ABLE TO WORK ON OUR PAYROLL AS A W-2 *** *** WE WILL SPONSOR H1-B VISA'S *** Project Description: Role Description: The Multi-Channel Customer Marketing (MCCM) Operations team supports US Commercial profitable growth...
REGULATORY AFFAIRS LABELING SPECIALIST REQUIREMENT #16-01053 RECRUITER: MELISSA GIUSTI JOB LOCATION: JERSEY CITY, NJ JULY 5, 2016 *** CANDIDATES MUST BE ABLE TO WORK ON OUR PAYROLL AS A W-2 *** *** WE WILL SPONSOR H1-B VISA'S *** Project Description: Under general supervision, responsible for the preparation of high-quality labeling documents for submission to the US Food and Drug Administ...
CLINICAL TRIAL ASSISTANT REQUIREMENT #16-01010 RECRUITER: MELISSA GIUSTI JOB LOCATION: JERSEY CITY, NJ JUNE 27, 2016 *** CANDIDATES MUST BE ABLE TO WORK ON OUR PAYROLL AS A W-2 *** *** WE WILL SPONSOR H1-B VISA'S *** Project Description: Responsible for supporting the Clinical Trial Management/operational study team to manage the various aspects of the operational execution and delivery of...
Bioclinica, Inc. is looking for intelligent, creative and dedicated professionals to join our growing team. We are a company that values technical excellence, teamwork and a commitment to success. We employ cutting edge technology to provide our customers with industry leading solutions and are currently seeking to fill the position of Imaging Operations Associate to work out of our Newark, CA off...
One of the fastest growing global Pharmaceutical companies focused in biosimilars is looking for strong Regulatory Affairs professionals to join their rapidly growing team based out of their Northeastern New Jersey location. With a robust portfolio of over 200 pharmaceutical products in development - don't miss this opportunity to join one of the best in the industry! Roles & Responsibilities: S...
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, ...
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...
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...
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...