• Merck & Co. (North Wales, PA)
    …the Research & Development pipeline and realize its full potential. The Associate Director is expected to provide project management leadership and drive ... is expected to contribute to ongoing business process improvement and talent development in Global Project and Alliance Management (GPAM). Primary… more
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …other research areas centered around rare diseases and immune disorders. Summary The Associate Director, Program Management is a senior position responsible for ... risks as well as achieving overall project level quality metrics. An ideal Associate Director, Program Management must have the expertise and leadership to… more
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  • Merck & Co. (Rahway, NJ)
    …Biologics Analytical Research & Development department of our Research & Development Division is seeking applicants for an Associate Principal Scientist ... position available at its Kenilworth, New Jersey research facility.- The Associate Principal Scientist is a laboratory-based scientific role tasked with solving… more
    HireLifeScience (09/12/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …team, the Associate Director of Global HR Communications and Change Management will be responsible for developing clear and effective communications for ongoing ... ensure the development and execution of strategic change communication plans. The Associate Director will contribute to the development of these plans and… more
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …solves and negotiates in most service types, studies, and programs- Responsible for the development and management of other ad hoc special projects as they arise ... plans for specific categories under the direction of the head of category management , for the creation, execution, tracking of strategies. Includes working under a… more
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  • Novo Nordisk Inc. (WA)
    …to providing medical education and collecting data to support efficacy and new product development , CMR is involved. The one thing that keeps us all marching to the ... scientific integrity; regulatory and process compliance) for monitoring and site management activities. Takes ownership to deliver upon near-term North America… more
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  • Merck & Co. (North Wales, PA)
    Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical Development , Ophthalmology will focus on driving strategy, development , and ... of the disease area, the functions and processes relevant to drug development , and project management principles as applicable to the pharmaceutical… more
    HireLifeScience (09/04/24)
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  • Tris Pharma (Monmouth Junction, NJ)
    …have an immediate opening in our Monmouth Junction, NJ facility for an Associate Director, Alliance Management .Tris Pharma has a long track record of ... spanning many departments across all stages of the product lifecycle. The Associate Director, Alliance Management will be accountable for managing alliances… more
    HireLifeScience (08/26/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …other research areas centered around rare diseases and immune disorders. SummaryThe Associate Director, Consumer Marketing serves as the patient, brand and product ... position will interact with all functions involved in the development and execution of the annual brand plan including...success of product messaging, programs and promotional effort. The Associate Director is also responsible for a broad array… more
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …Recruitment, Payroll, Performance Management , Compensation Management , Learning Management , Success Planning and Development . required- 1 or More Years ... research areas centered around rare diseases and immune disorders.Summary The Associate Director of ERP Applications is responsible for overseeing and enhancing… more
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  • Aequor (Thousand Oaks, CA)
    …and internal suppliers within Contract Manufacturing Organization. The Contract Development and Manufacturing organization is seeking a highly qualified candidate ... to support analytical assay outsourcing associated with execution of external development and clinical supply. The position will be a key enabling role in a high… more
    HireLifeScience (09/04/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …creation and review including: (A) overseeing the day-to-day operation of contract management procedure for the Commercial and Development divisions; (B) ... system.Responsibilities- Oversees and provides day-to-day operation of the contract management process for the Commercial and Development Divisions. Acts… more
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …The Associate Director will lead the execution and lifecycle management of Global Medical Affairs' externally sponsored clinical research (ESR) initiatives, ... guidelines requiredExcellent communication, organizational, and problem-solving skills requiredProven people management experience, demonstrating effective leadership and team development more
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  • Aequor (Thousand Oaks, CA)
    …Anticipates and resolves conflict situations in a win-win outcome. Contributes to study management and the development of study documents as appropriate as well ... IS )Ideal candidate: Must have Smartsheet experience, Must have Agile project management and Agile frameworks (Scrum, Kanban, SAFE, etc.), BA/BS in Computer Science,… more
    HireLifeScience (09/04/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …global sites. These business functions include: Clinical Operations, Clinical Development , Biostatistics and Data Management , Regulatory Affairs, Quantitative ... areas centered around rare diseases and immune disorders.Job Summary Deliver the development and implementation of informatics systems and programs to support the… more
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …research areas centered around rare diseases and immune disorders. Job Summary: The Associate Director of Regulatory Writing is a key role responsible for producing ... provide scientific and strategic insights at the study team level. The Associate Director of Regulatory Writing must possess advanced knowledge of BLA/MAA… more
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …simultaneously. preferred- 4 or More Years Extensive experience in project management , process, product, and/or analytical development activities and ... defined based on the project needs and the respective development stage of the project. The CMC Lead will...timeline, achievement of defined milestones and overall project risk management . He/she will assess project issues and develop resolutions… more
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  • Daiichi Sankyo, Inc. (Seattle, WA)
    …research areas centered around rare diseases and immune disorders. Summary: The Associate Director, Field Reimbursement (ADFR) is a critical front-line member of the ... landscapes with expertise in formulary decisions, reimbursement policy, utilization management criteria, prior authorization processes and appeal requirements. Develop… more
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  • Daiichi Sankyo, Inc. (Boston, MA)
    …research areas centered around rare diseases and immune disorders. Summary: The Associate Director Field Reimbursement (ADFR) is a critical front-line member of the ... landscapes with expertise in formulary decisions, reimbursement policy, utilization management criteria, prior authorization processes and appeal requirements. Develop… more
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …equal opportunity employer including veterans and people with disabilities.SummaryThe Associate Director will be responsible for developing and implementing Clinical ... & Simulation plans from FIH to post registration. Responsibilities include the development of Clinical Pharmacology and Modeling and Simulation plans, design and… more
    HireLifeScience (09/13/24)
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