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Associate Principal Scientist, Preclinical Development, Formulation Scientist
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health ..
Develop and conduct processes for the manufacture of novel nanoparticle and/or dry powder formulations
Perform characterization techniques to assess formulation physicochemical properties
Maintain proper documentation of experimental procedures and results
The role will report to the Director, Strategic Market Access and will be responsible for Oncology Market Access deliverables with the Business Franchise (BF) and the Brand/Disease teams. This role includes ..
The Sr. Regulatory Associate is responsible for performing the role of the US Promotional Review Committee (PRC) coordinator for assigned product(s) to ensure that all promotional, nonpromotional and internal ..
nOur client, a pharmaceutical company, is currently seeking a Associate Director Regulatory Affairs Will be responsible for development and implementation of regulatory strategies of new drugs/biologics in the US including monoclonal ..
Novartis is recruiting for an Associate Director, Specialty Pharmacy Services. This role is a field based role and can be located in the Midwest or Southeast. Preferred location would be Midwest.
Novartis - Job details
The job will lead social media strategies and tactics supporting franchises and brands in disseminating product/franchise/Novartis franchise key messages to target external audiences including patients and caregivers ..
The Associate Clinical Development Director (Assoc. CDD) is responsible for the scientific and clinical strategy of assigned clinical trials, scientific monitoring, and reporting of quality data. Maybe responsible for the clinical ..
Clinical Research Associate/Clinical Trial Associate- Berkeley Heights NJ 07922rnJob Overview:rnCollect and organize data obtained during studies andu00a0trialsu00a0conducted. Coordinate and process results gained from long-term testing of drugs, products and medical procedures.rnResponsibilities:rnrntReviewing ..
Associate Director, Regulatory Affairs
Mapi is a leading global organization, offering evaluation and support of therapeutic strategies. With offices worldwide, Mapi provides high quality and efficient operations ..
The primary role of the CSO Operational Capacity and Planning Manager (OPCM) is to act as the key CSO planning interface for the CSO Project Leader, the TMCP Lead (CSD from ..
Biostatistician, Global Biometric Sciences
The biostatistician is a member of cross-functional development teams and contributes to trial design, protocol development, analysis planning, interpretation of results, and preparation of ..
Planning and Execution Lead, Global Biometric Sciences
This position manages the Biometric processes of drug development projects including key aspects such as clinical trials reporting and regulatory filing ..
nRequisition ID 49808BRTitle ASSOCIATE DIRECTOR - MARKET ACCESS - PRICING & CONTRACTING STRATEGYJob Category Market AccessJob Description Purpose* Develops and executes the pricing and contracting strategy for a key Novo Nordisk ..
nRequisition ID 50417BRTitle Associate Manager, Government Contracts - PricingJob Category FinanceJob DescriptionPurposeAssists Sr. Manager and/or Director of Government Pricing and Compliance in leading an analytical team in the development and implementation ..
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Associate Director Market Research New Products
Your tasks and responsibilities
The primary responsibilities of this role, Associate
Director Market Research New Products, are
Independently plan, implement, ..
FLORHAM PARK , New Jersey
Full Time - Experienced
Fairleigh Dickinson University School of Pharmacy seeks applicants for a Clinical Assistant / ..
Lead Governance operations to ensure the process runs seamlessly, and that appropriate guidance is provided across the organization to ensure compliance with Novartis standards.
• Operations Lead – Lead ..