- Daiichi Sankyo, Inc. (Bernards, NJ)
- …The qualified candidate will provide knowledge-based coordination, authoring, and management of Dose Preparation Instructions in support of clinical studies ... Collaboration with external stakeholders (eg, research pharmacists, clinical study partner management ) may also be required. Additionally, the candidate will also… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Legal Operations, Innovation & Technology team's responsibilities include financial management , program law firm management , legal records ... and increasing overall operational effectiveness.We are seeking a dynamic and experienced Associate Director of Outside Counsel and Vendor Management to join our… more
- Eisai, Inc (Raleigh, NC)
- …a difference. If this is your profile, we want to hear from you. The Director Western Supply Chain Management (SCM) Unit is accountable and/or responsible for ... The Director will develop colleagues with expertise in relationship/project management , contract review and negotiation, demand planning, and logistics to manage… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. Job Summary: The Director of Data Management (DM) Reporting provides leadership in Data ... data protection, operational metrics, and clinical trial quality and risk management reporting requirements that adhere to programming standards and specifications… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Summary: The Associate Director , Laboratory Data Management is accountable for the end-to-end delivery ... usage, and disease-specific requirements to DM standards teams and program teams.- Advise Manager, Laboratory Data Management ...and program teams.- Advise Manager, Laboratory Data Management on complex textbook range and unit requests as… more
- Eisai, Inc (Nutley, NJ)
- …this is your profile, we want to hear from you. The Associate Director , Clinical Programming must have expertise in addressing technical challenges in the ... skills in SAS systems and application development and experience. The Associate Director must be a highly specialized individual contributor or functional manager… more
- Merck & Co. (Rahway, NJ)
- …As a member of the Device Quality & Regulatory QMS group, the Associate Director will participate in and/or lead various initiatives in support of our QMS Purchasing ... Controls and Device Supplier Management objectives and build QMS capabilities that touch every...aspect of our business processes, systems, and data.The Associate Director will collaborate and interact with cross-function teams to… more
- Merck & Co. (Rahway, NJ)
- …and Technology Organization. This position is responsible for providing strategic program leadership, technical expertise, and project management in the ... Job DescriptionThe Associate Director - Device Tech Transfer is a leadership role...and quality and regulatory compliance. Essential Duties and Responsibilities: Program Leadership and Technical Project Management :Provide … more
- Merck & Co. (Rahway, NJ)
- …clinical development teams and the operational/executional arms within the business. The Program Clinical Supplies Project Manager ( Program CSPM) serves as the ... spokesperson at clinical and development related meetings.- Working independently, the Program CSPM designs strategic and operational plans for all clinical supply… more
- Merck & Co. (Rahway, NJ)
- …therapeutic areas and modalities to drive portfolio impact from discovery through life-cycle management . The team is externally visible and continues to be at the ... drive pipeline impact and lead a talented group of pharmacometricians.This Senior Director is expected to be an experienced pharmacometrician with a strong,… more
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