R & D Jobs in East Hanover, New Jersey

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217 East Hanover, NJ R & D jobs found on Monster.

Jobs 1 to 20 of 217
Informed Consent and Study Start-Up Specialist needed for a contract opportunity with Yoh's client located in East Hanover, NJ. The Big Picture - Top Skills Should You Possess: - Experience with HIPPA - Experience starting up clinical trials - Basic knowledge of consents What You'll Be Doing: - Review and negotiate the legal sections of the ICF pre-IRB submission, post IRB comments, confirms the l...
Clinical Research Scientist needed for a contract opportunity with Yoh's client located in East Hanover, NJ. The Big Picture - Top Skills You Should Possess: - Strong scientific or clinical background What You'll Be Doing: - Assist or coordinate and collect data from patient charts, medical records, interviews. Obtain data from outside sources (physician offices/hospitals) as needed for data colle...
Job Number: 419126 Clinical Research Scientist (3918257) 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) and those with...
Job Number: 419085 Biostatistician III (3917315) Duties: 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;...
Biostatistician needed for a contract opportunity with Yoh's client located in East Hanover, NJ. Top Skills Should You Possess: - Clinical Trial experience - Strong SAS knowledge What You'll Be Doing: - Provide statistical input for planning, analysis and reporting of multiple project activities. - Take responsibilities as trial statistician with minimal guidance. - Provide statistical consultatio...
TechData is hiring SAS Programmer (Some positions can be telecommute), Biostatistician(Some can be telecommute), Clinical Research Scientist/Clinical manager, Contract Specialists, Outsourcing Manager, Informed Consent Setup and study start up, Sr. Clinical Data Managerfor our pharmaceutical clients in Northern NJ. Please see below requirements and send your resume to: *****...
Expert Clinical Manager I – 5 month contract Under the guidance of the Project Operations and Compliance (POCO) assist with organizing a structure in Novartis document and tracking systems (CREDI and clinadmin) for all our compassionate use programs. Requirements BS or MS degree required. At least 3 years’ experience in pharmaceutical industry or CRO. Be able to understand clinical operations and...
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...
Contract Coordinator – 6 month contract Responsible for resolving contract processing issues. Liaising with Request to Pay (RTP), Outsourcing Managers, Vendors and Finance Department. The Contract Coordinator may be responsible for drafting and/or procuring and processing partially executed contracts, amendments and agreements. The main point of contact, tracks the process and ensures completion o...
Associate Global Correlative Sciences Leader – 5 month contract Contributes to Afinitor and PI3K programs' biomarker research by supporting the programs' Correlative Science Leaders. Key expertise includes familiarity with cancer genetic (breast cancer in particular), next generation sequencing (NGS), and PI3K/AKT/mTOR pathway. Requirements PhD in cancer genetics, cancer biology and molecular biol...
Seeking multiple Project Managers for consulting positions at a major pharmaceutical client in East Hanover, NJ 07936. Key components of the responsibilities are as mentioned below: · Manages projects from scope definition to deployment · Liaisons with internal and external client’s · Defines project scope, approach and understands client reporting requirements for adverse events · Creates strateg...
TechData is hiring SAS Programmer (Some positions can be telecommute), Biostatistician(Some can be telecommute), Clinical Research Scientist/Clinical manager, Contract Specialists, Outsourcing Manager, Informed Consent Setup and study start up, Sr. Clinical Data Managerfor our pharmaceutical clients in Northern NJ. Please see below requirements and send your resume to: *****...
Our client, a large pharmaceutical company, is currently seeking a DESKTOP PUBLISHER. 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 NIBR a...
*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...
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...
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...
Global pharmaceutical company based in NJ seeking a Director, Integrated Insights. Lead and set the strategic direction for an insights driven analytics and primary research team that proactively helps drive growth. Role is critical to helping drive growth with in-line and launch products. This person will lead an Integrated Team of Insights (Primary Research) and Analytics associates who work dir...
A highly reputable and distinguished pharmaceutical corporation is currently looking for Clinical Data Managers to work in East Hanover, New Jersey. Job Description: Responsible for providing timely and professional ongoing quality management of clinical trial data by identifying errors/inconsistencies in CRF data and ensuring their resolutions in order that databases can be declared clean and loc...
PHARMACEUTICAL INDUSTRY EXPERIENCE REQUIRED Pharma Customer Service Specialist – Customer Relations Specialist – CRM LOCATION: Whippany, NJ 07981 Customer Service Specialist / Customer Relations Account Representative This is a direct hire position which offers a competitive compensation package, 401K, and full benefits. If interested and qualified, please apply by emailing your Word .doc resume a...
Mondelēz International LLC is a whole new company that has been reimagined with a single focus in mind: create delicious moments of joy by sharing the world’s favorite brands. Launched on Oct. 1, 2012, and employing around 100,000 people around the world, Mondelēz International comprises the global snacking and food brands of the former Kraft Foods Inc. While Mondelēz International LLC is new, our...
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