- Merck & Co. (Rahway, NJ)
- …advancing our company's contribution to global medical innovation. Job Description: The Associate Director , IT SOX Program Manager plays a key role within the ... IT Risk & Compliance Programs function. Responsible for the end-to-end oversight of the IT SOX program , the IT SOX Program Manager drives the program 's… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …quality listings, SAP, DM plan, Reviews patient population and protocol compliance for consistency with study strategy, develops biomarker strategy in collaboration ... Leads broad collaboration with KOLs or major institution, eg NCI.Scientific, Program related: Integrated Study Team (IST) representative: Creates early development… more
- Merck & Co. (Rahway, NJ)
- …with the company's business goals, and quality and regulatory compliance .-Essential Duties and Responsibilities: Program Leadership and Technical Project ... Job DescriptionJob Summary: -The Director of Device Technology Transfer is a key...Technology Organization. This position is responsible for providing strategic program leadership, technical expertise, and project management in the… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. Summary The Director Global Medical Affairs Oncology (GMA), ADC, under the direction of the ... Senior Director , GMA Oncology ADC (Global Medical Affairs team lead...lead for compound), is responsible for assisting with defining compound/ program medical strategies and for leading select medical affairs… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Are you ready to realize your potential? The Position The Executive Director , Sales Innovation and Deployment Strategy is responsible for leading an innovation ... National and Operations leaders. Has direct supervisory responsibility for a Senior Director of Commercial Execution, Pharmacy Execution team and Virtual Sales team… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders.Summary: The Associate Director , Regional Marketing Conventions & Field Programs will be responsible for ... more, while ensuring adherence to DS policies and procedures. The Associate Director , Regional Marketing Conventions & Field Programs is responsible for managing the… more
- Merck & Co. (Rahway, NJ)
- Job Description Position Description: Associate Director , Site Services Procurement (NORAM) This Procurement Associate Director role will be a member of the ... Global Site Services Procurement team include the Integrated Facility Management (IFM) Program for all our Company's facilities worldwide, the MRO Integrator … more
- Merck & Co. (Rahway, NJ)
- … mindset.Essential Knowledge, Duties & Responsibilities for the Director Include:Biopharmaceutics expertise supporting delivery of small molecule, peptides ... oral and non-oral portfolio. Within Biologics and Biopharmaceutics, the Biopharmaceutics Director will influence the strategy, lead activities, and develop a team… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Summary: The Associate Director will lead the execution and lifecycle management of Global Medical Affairs' ... collaborative studies. Ensure projects align with strategic goals and compliance standards from initiation through completion.Operational Strategy: Develop and… more
- Daiichi Sankyo, Inc. (Seattle, WA)
- …areas centered around rare diseases and immune disorders. Summary: The Associate Director , Field Reimbursement (ADFR) is a critical front-line member of the DSI ... in a compliant/ethical manner. Handles PHI appropriately by ensuring compliance with HIPPA regulations, laws and internal company guidelines.Control business… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders.Summary The Associate Director , RACMC Portfolio Products, will be responsible for regulatory CMC (Chemistry, ... regulatory process optimizations on relevant topics.Responsibilities- Supports CMC regulatory compliance activities for portfolio biologics to meet US, International… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for given commodities/business areas and leading the overall supplier relationship management program for DSI, for DS products and alliances. Cultivates a high ... as the Project Management Owner for DSI's overall Supplier Relationship Management Program (SRM) with Tier 1 suppliers which includes robust comprehensive supplier… more
- Tris Pharma (Monmouth Junction, NJ)
- …from you.We are hiring at our Monmouth Junction NJ Headquarters for a Senior Director to lead our small, but productive, Marketing team.The Senior Director , Head ... materials, activities and related communications and programs are in full compliance with Medical, Legal, Regulatory and Corporate guidelines; Establishes, oversees… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …quality listings, SAP, DM plan, Reviews patient population and protocol compliance for consistency with study strategy, Develops biomarker strategy in collaboration ... Leads broad collaboration with KOLs or major institution, eg NCI.Scientific, Program related: Integrated Study Team (IST) representative: Creates early development… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …listings, SAP, Data Mgmt plan; Reviews patient population and protocol compliance for consistency with study strategy; Develops biomarker strategy in collaboration ... Initiates contact w/KOL and prepares material for KOL interactions on a program based need; Involvement with in-licensing and acquisitions on individual due… more
- Insmed Incorporated (Louisville, KY)
- …day-to-day workload of Case Management team; reallocate resources where necessaryEnsure team compliance with program Business Rules, SOPs and other relevant ... is the exact vision of the Insmed Patient Support Program and the reason we are seeking top talent...are seeking top talent for the role of Associate Director of Case Management. Patients are the core of… more
- Insmed Incorporated (San Diego, CA)
- …Best Medium Workplaces™ lists.OverviewJoin the Technical Operations team as an Associate Director of MSAT where you will support pipeline programs that change lives. ... subject matter expert during external and internal regulatory submissions and compliance inspections. Travel will be required to support person-in-plant activities… more
- Novo Nordisk Inc. (Boulder, CO)
- …applicable environmental, health and safety regulations. Relationships Reports to Associate Director , EHS at US headquarters in MA. Internal relationships include ... Essential Functions Manage the maintenance and implementation of safety programs, compliance plans, and initiatives with primary focus on laboratories as well… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: MCAAS Finance Leadership Development Program Finance at our Company is committed to developing future leaders through its ... Finance Leadership Development Program (FLDP). Individuals are provided with an entry point...this includes a deeper knowledge of internal controls, business compliance , and risk management. Individuals will be based in… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …improvements and seek agreement through consensus management. Relationships Reports to an Associate Director / Director within the NNI Procurement Team and will ... and helps others do the same Supports the Novo Nordisk Supplier Diversity program and promotes the inclusion of diverse suppliers in all sourcing initiatives Manages… more
