Featured Job
-
Job Removed or Not Found
Related Jobs
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Successful candidates will be able to meet the qualifications below with or without a reasonable accommodation.Education Qualifications (from an accredited college or
- Novo Nordisk Inc. (Boulder, CO)
- …Bachelor's degree in Science, Business, or related discipline with five (5) years of experience in pharmaceutical or related industry required Master's degree with three
- Merck & Co. (Rahway, NJ)
- …include statistical experimental design & data analysis, authoring of technical reports, regulatory submissions and patent applications. -Active participation on
- Merck & Co. (North Wales, PA)
- …: This position supports statistical programming activities for late stage drug/vaccine clinical development projects. This may include leadership of one or more
- Aequor (Thousand Oaks, CA)
- …Bachelor's Degree in Life Sciences, Business, Operations or Industrial Engineering. Experience in Biotech or pharmaceutical operations, manufacturing, process
- Novo Nordisk Inc. (Plainsboro, NJ)
- …10-20% overnight travel requiredDevelopment Of People:Ensure all direct reports have Individual Development Plans (IDPs) with annual goals aligned to business priorities,
- Genmab (NJ)
- …experience, and location. Also, certain positions are eligible for additional forms of compensation, such as discretionary bonuses and long-term incentives. When you join
- Eisai, Inc (Nutley, NJ)
- …The Executive Director, Regulatory Affairs will provide leadership and direction for the global regulatory aspects of Eisai's products under development and post approval
- Genmab (NJ)
- …in leading the programming efforts of at least one study are in scope.The Programming Manager will support the Data Management, Statistics, Drug Safety, Medical, Clinical
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …CDx development : Provide critical strategic and tactical regulatory guidance for CDx/IVD development and CDx submission plan for each country/region, both before and