Teva Pharmaceuticals USA Jobs in Chester

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19 Teva Pharmaceuticals USA jobs in Chester, Pennsylvania found on Monster.

Jobs 1 to 19 of 19
Overview The GMP Scientist will develop, validate and perform analytical testing activities within a GxP-compliant laboratory to support pre-clinical studies, clinical development, method transfer, process transfer, process improvement, scale-up and process validation. The Scientist should possess a practical understanding of pharmaceutical (i.e. small molecule) drug development and GxP requiremen...
Overview We are seeking a highly motivated Principal Scientist with a strong background in Oncology biomarkers and personalized medicine. You will provide biomarker assay expertise to support pre-clinical and worldwide clinical trials in all phases of development that have biomarker needs, exploratory, surrogate end point, patient stratification, safety, efficacy with a multi-disciplinary team of...
Overview The incumbent provides regulatory medical writing expertise to the Clinical Development and Medical Department (within specified therapeutic areas) in the preparation of clinical research documentation in support of drug development, product registrations, and product marketing. The incumbent oversees/manages/plans the preparation of clinical regulatory documents for specific drug project...
Overview The incumbent provides regulatory medical writing expertise to the Clinical Pharmacology department in the preparation of clinical research documentation in support of drug development, product registrations, and product marketing. The incumbent oversees/manages/plans the preparation of clinical regulatory documents for specific drug projects, which includes managing medical writing activ...
Overview Teva Biopharmaceuticals, USA (TBU) is responsible for developing innovative and biobetter biologics for Teva Pharmaceuticals—the largest generics company in the world with over $20 billion in annual revenue. We currently are developing 8 products in various stages of clinical development from IND through BLA filing including, innovative mAbs, extended half-life biobetters and biosimilar p...
Overview This is an experienced Ph.D. level position requiring the individual to have laboratory expertise in synthetic organic chemistry. This position requires full use and application of chemical principles, theories and techniques applied toward a wide range of difficult problems across projects within one or more areas of expertise. The individual will be responsible for conduct, evaluation a...
Overview The primary responsibility of the Sr.CPM is to oversee and manage global trials for all clinical phases, in partnership with other functions and the Regional Clinical Trial Managers (RCTMs). The Sr.RCTM is also responsible to provide professional expertise and leadership through leading global departmental tasks, taking initiatives in improving GCO processes and providing mentoring, train...
Overview Position Summary: This Sr. Manager, Market Research position will provide MR, competitive intelligence, forecasting and reporting support primarily for Neurodegenerative Diseases.This position will report to the Director of GMI, CNS. Global Medicine Insights is a part of the Global Specialty Medicines organization and is charged with ensuring that the current and future needs of and behav...
Overview To support the Commercial Operations group with forecasts, budgets and day to day analysis. This person will partner with the various Directors and Brand teams to drive value through strong analytics. In addition, this person will partner with Purchasing to evaluate opportunities for savings as well as monitor policies. Responsibilities Gather, consolidate, and analyze, reports and explai...
Overview Teva’s Manager, Trade Strategy Development is responsible for the evaluation, development and implementation of market driven trade and distribution strategies for Teva’s in-line and pipeline branded specialty products. He/She will be instrumental in providing objective support and rationale for channel strategies needed to optimize the commercial effectiveness of Teva’s products. The evo...
Overview Reporting to the Vice President and Head of US Medical Affairs, Medical Directors group, the Medical Director/Sr. Director Pain will be responsible for development of the medical strategy for all Pain products’ design and execution of supporting initiatives in the United States. The incumbent will be charged with developing and providing a rigorous scientific and medical foundation for ac...
Overview The Project Manager role within the Project Management Office is responsible for providing project management to global product development teams. The Project Manager is required to work effectively with their assigned teams, across functions, divisions, organizational levels, and companies to ensure that efficient and productive project management is provided to maximize the value of the...
Overview Develop, coordinate and execute regulatory strategies in a team environment for new product development and registration globally, as well as line extensions or new indications for marketed products. The individual will interact with global regulatory counterparts on the development of ex-US submission strategies and provide support as needed. Interact with FDA and ex-US health authoritie...
Overview Teva’s New Therapeutic Areas & Initiatives is a newly created team, part of Teva’s Global Specialty Medicines organization and is charged with creating the new therapeutic areas from which Teva’s future growth will be driven, as well as leading, planning and execution Teva’s development in to a Pharma 3.0 company. There are two groups within the team, one group of commercial leaders that...
Overview Teva Pharmaceutical Industries Ltd. (NYSE: TEVA) is a leading global pharmaceutical company, committed to increasing access to high-quality healthcare by developing, producing and marketing affordable generic drugs as well as innovative and specialty pharmaceuticals and active pharmaceutical ingredients. Headquartered in Israel, Teva is the world's leading generic drug maker, with a globa...
Overview To generate high value NTE commercial opportunities that support the development of strategic platforms/ constellations. Will identify key unmet medical/ commercial needs that drives innovative product utilization. Strong focus on patients, physician, payor insights. Responsibilities -Lead NTE commercial strategic platform ideation across strategic TAs -Collaborate and gain alignment with...
Overview Initiate and maintain the Clinical QA program in support of Teva's Branded Pharmaceutical Products R&D business Responsibilities Develop and Manage all therapeutic area quality audit programs with the oversight by the Director/Sr. Director Adviser to Clinical trial R&D teams (clin ops, data management, PV, statistics) routine advising independently, advising on major compliance issues wit...
Overview The purpose of the Manager, ISSs & Phase IV Coordination, is to function as the lead role in the management of the investigator sponsored studies (ISS) program and tracking of the ISSs and Phase IV studies. The Manager will manage, monitor and track ISS within the external web-based portal for the global intake, review and approval by the Investigational Review Committee (IRC). The Manger...
Overview Position Summary: This role is responsible for developing and leading brand communications for assigned therapeutic areas as a part of the communications team for NA Specialty Medicines. Supporting the Director, Brand Communications and leadership of the therapeutic areas, directs and manages brand communications, including strategy and execution, for assigned therapeutic areas. This incl...
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