• Merck & Co. (Rahway, NJ)
    …also be critical for this role. This role will support the Business of IT program and report to the Executive Director of IT Strategic Communications and Change ... to get the job done? If so, the Associate Director , Business of IT Strategic Communication and Change Management...and Change Management Lead for the Business of IT program , you will play a critical role in driving… more
    HireLifeScience (06/06/25)
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  • Merck & Co. (Rahway, NJ)
    …origin.We are seeking a dynamic and strategic leader to join our team as a Director of Program Management and Execution Excellence. We are looking for a season ... Program manager with a passion for driving impactful business...a related field.Minimum of 10 years of experience in program /project management, with at least 5 years in a… more
    HireLifeScience (06/05/25)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionThe Executive Director (Distinguished Scientist) has primary responsibility for the planning and directing of clinical research activities involving ... Atherosclerosis section of the Atherosclerosis & Metabolism therapeutic area. The Executive Director will manage and oversee the entire cycle of late stage clinical… more
    HireLifeScience (06/07/25)
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  • Merck & Co. (Rahway, NJ)
    …Operations, Innovation & Technology team's responsibilities include financial management, program law firm management, legal records and information management, ... increasing overall operational effectiveness.We are seeking a dynamic and experienced Associate Director of Outside Counsel and Vendor Management to join our Legal… more
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  • 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
    HireLifeScience (05/29/25)
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  • Merck & Co. (Rahway, NJ)
    …with a passion for biologics? We're looking for a dynamic and visionary- Director , Drug Substance Leader-to drive innovation and excellence across our Biologics ... Commercialization portfolio Support CMC teams and align resources to deliver on program priorities Mentor and develop a team of scientists focused on biologics… more
    HireLifeScience (06/05/25)
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  • Merck & Co. (Rahway, NJ)
    …team of approximately 10-15 scientists in Rahway NJ, who lead multidisciplinary program teams and execute laboratory activities. The primary objective of the ... this individual will support late stage and commercial large molecule biologics program activities. The individual will be responsible for leading a team of… more
    HireLifeScience (06/07/25)
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  • Merck & Co. (Rahway, NJ)
    …at our Company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas.This Associate Director ... continuous basis in decision making and driving pipeline impact. The Associate Director will perform job duties independently with minimal supervision and/or lead… more
    HireLifeScience (05/29/25)
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  • Merck & Co. (Rahway, NJ)
    …innovate, iterate, and problem-solve.Cross-Functional Collaboration:-Unite diverse teams to achieve program goals as One Team. Champion compliance and safety; ... promote a culture of diversity, inclusion, and equity. Experience and aptitude to lead, work, and collaborate in internal and external cross-functional, matrixed teams.Problem Solving:-Remove roadblocks, resolve conflicts, and escalate issues when… more
    HireLifeScience (06/05/25)
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  • Merck & Co. (Rahway, NJ)
    …its customers, and shareholders. The scope of this group includes strategic program management, enterprise strategic planning, risk management, as well as strategic ... ensure effective implementation and cross-functional engagement. Position Description: The Director of Commercial Strategy will support strategy development for… more
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionDescription The Associate Director position's core responsibilities are to oversee our Company's compliance related to customs country of origin. In ... are to oversee our company's customs country of origin program and lead efforts related to global customs origin...of our company's Free Trade Agreement usage. The Associate Director position's key responsibilities are around these programs; as… more
    HireLifeScience (05/28/25)
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  • Merck & Co. (Rahway, NJ)
    …Reporting to the Customs & International Trade (CIT) Valuation Associate Director , the Senior Specialist position's core responsibilities are to oversee our ... Company's Global Value for Customs Purposes (VCP) program and conduct Proof of Payment activities. CIT is...to manage and monitor compliance with our Company's VCP program . This program provides guidance in customs… more
    HireLifeScience (05/28/25)
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  • Merck & Co. (Rahway, NJ)
    …presentations to governance committees and other internal audiences.Partnering with director -level management to develop and execute scientific and enterprise ... strategies.-Proactively identifying and escalating program risks.Fostering strong collaborations with internal stakeholders and external partners by actively… more
    HireLifeScience (06/03/25)
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  • Merck & Co. (Rahway, NJ)
    …DescriptionReporting to the Customs & International Trade (CIT) Tariff Classification Associate Director , the Senior Specialist will work closely with our Research & ... IndicatedValid Driving License:NoHazardous Material(s):n/aRequired Skills:Audits Compliance, Audits Compliance, Compliance Program Development, Crisis Management, Detail-Oriented, Ethical Compliance, Government Agencies,… more
    HireLifeScience (05/28/25)
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  • Merck & Co. (Rahway, NJ)
    …Scientist is a senior scientific role tasked with working closely with the group Director to define group strategy and to lead a team of scientists in solving ... transfer of assays. Plan assay optimization and documentation to meet program deadlines.Authoring and reviewing internal technical reports, sections of regulatory… more
    HireLifeScience (04/26/25)
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  • 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 ... Join a Legacy of Innovation 125 Years and Counting! Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging… more
    HireLifeScience (05/18/25)
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  • Merck & Co. (New York, NY)
    …are seeking a Growth and Improvement minded Oncology Regional Medical Scientific Director that can help drive our Strategic Operating Priorities. Invent-- Pursue the ... must reside in the territory.Strategic Summary The Oncology Regional Medical Scientific Director is a credentialed (ie, PhD, PharmD, DNP, MD) oncology expert who… more
    HireLifeScience (06/03/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …areas centered around rare diseases and immune disorders. Summary:The Associate Director , Oncology Value & Market Dynamics Training Manager is responsible for ... to access for patients across our portfolio of products. The Associate Director will develop, in partnership with other key stakeholders, innovative solutions for… more
    HireLifeScience (05/08/25)
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  • 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 of ... defense meetings.- Provides laboratory data expertise and guidance to the program teams regarding the laboratory data activities and deliverables.- Accountable for… more
    HireLifeScience (05/13/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …of Clinical Development processes. Job Description:Execute an overarching safety program tailored for AEs from end-to-end: understanding predisposing non-clinical ... and clinical factors, diagnosis, effective management during clinical trials and beyond in post approval setting.Responsible for the execution of key safety initiatives aimed at preventing, mitigating, and addressing critical safety issues including but not… more
    HireLifeScience (05/21/25)
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