- Merck & Co. (North Wales, PA)
- Job DescriptionThe Director , Regulatory Affairs Liaison, is responsible for development and implementation of global regulatory strategy for their ... for all submissions and associated documentation. Provides expertise as worldwide regulatory representative to Product Development Teams and regulatory… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …innovative and flexible approaches to achieve development goals, advise on development strategies, and deliver on associated regulatory activities Lead the ... advanced degree is strongly preferred Minimum of 10 years drug development /FDA/ regulatory related industry experience required Demonstrated knowledge of global… more
- George Washington University (Washington, DC)
- I. JOB OVERVIEW Job Description Summary: The Director , Regulatory Oversight position reports to the Associate Provost Research Integrity and Compliance (AP-RIC) ... administrative oversight of the research radiation and laser safety programs. The Director , Regulatory Oversight works closely with Office of Research Integrity… more
- Fidelity TalentSource LLC (Boston, MA)
- …desks, middle office teams, compliance, systems development squads and other business partners that have an impact on Regulatory Reporting. \u00A0\u00A0You ... Capital Markets trading floor? \u00A0We are looking for a Director of Regulatory Reporting, a leadership position...and respond to inquiries and examinations, as needed.\u00A0 The Director will lead the development of a… more
- Merck & Co. (North Wales, PA)
- …The Director will manage the entire cycle of clinical development , including: study design, placement, monitoring, analysis, regulatory reporting, and ... regulatory affairs, statistics, and manufacturing to manage clinical development projects; andAssist the Senior Director , Executive Director… more
- Merck & Co. (North Wales, PA)
- …project work, the Associate Director is expected to contribute to ongoing business process improvement and talent development in Global Project and Alliance ... Job DescriptionThe drug development Project Manager is part of Global Project...organization of our company.- Position Description/Summary: The GPAM Associate Director , Project Manager, is a core member of Early… more
- Merck & Co. (Rahway, NJ)
- …cross-functional Device Working Group to ensure full integration of the device development activities with the clinical, regulatory , formulation, commercial and ... the program-specific design controls process and design history file development .Author and review relevant portions of the regulatory...then your employment may pose an undue burden to business operations, in which case you may not be… more
- Merck & Co. (Washington, DC)
- …execute public policy initiatives and advocacy related to our Company's US business interests.-The Associate Director is responsible for supporting the federal ... public policy, government relations, PAC and grassroots, and alliance development teams.- The Associate Director will monitor, analyze, and communicate… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …regulatory agencies. Supervise designated personnel. Relationships Report to the Director /Associate Director /Lead Regulatory Scientist/Sr. Manager ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one...and collecting data to support efficacy and new product development , CMR is involved. The one thing that keeps… more
- Merck & Co. (Rahway, NJ)
- …discovery and development (MIDD) to routinely enable efficient drug discovery/ development and/or regulatory decisions. The Pharmacometrics group within QP2 ... our company, this position offers an opportunity for the Director to drive pipeline impact and mentor/coach a talented...ability to understand how (MIDD can drive portfolio and regulatory decisions Deep knowledge of drug development ,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …head). They will coordinate with other TA functions including Medical Directors, Alignment Director , Program Development Director and the Medical Liaison ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one...and collecting data to support efficacy and new product development , CMR is involved. The one thing that keeps… more
- Eisai, Inc (Nutley, NJ)
- …through in neurology and oncology, with a strong emphasis on research and development . Our history includes the development of many innovative medicines, notably ... the strategy, prioritization and planning for IT systems and projects. Partner with business leaders, SMEs to understand how the functions operate today and what… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting… more
- Merck & Co. (North Wales, PA)
- …that gains response. And there's an important part for you to play:-Campaign Development LeadPut marketing strategy into action as you lead the development ... with copy, design, UX, architecture, internal legal, medical and regulatory teams in the co-design, co-creation, and execution of...campaign plans every step of the way. From creative development to approval and delivery to market, you'll have… more
- Merck & Co. (Rahway, NJ)
- …discovery and development (MIDD) to routinely enable efficient drug discovery/ development and/or regulatory decisions. The Pharmacometrics group within QP2 ... at ouor company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas.This Associate Director … more
- Eisai, Inc (Nutley, NJ)
- …messaging, and execution within scope of projects. Actively contribute to the development of the annual business plan. Requirements Bachelor's degree (BS/BA) ... and oncology, with a strong emphasis on research and development . Our history includes the development of...profile, we want to hear from you. The Associate Director , Omnichannel Marketing and Media position reports to the… more
- Tris Pharma (Monmouth Junction, NJ)
- …planning. The incumbent works cross-functionally with counterparts/teams in Clinical Development , Regulatory Affairs, Manufacturing, Quality, etc. to identify, ... potential risks mitigation, etc. Collaborates with appropriate clinical, medical, quality and regulatory counterparts and others across business to provide input… more
- Eisai, Inc (NJ)
- …communication/publication components of overall medical operating plan. The Medical Director provides strategic development , planning, implementation and ... and oncology, with a strong emphasis on research and development . Our history includes the development of...profile, we want to hear from you. The Medical Director , US Medical Affairs provides medical leadership for medical… more
- Merck & Co. (North Wales, PA)
- …Patient Assistance Foundation to ensure consistent Patient Assistance Programs referral business rules.Work with Marketing Operations in development of ... Job Description Position Description: - Director , United-States (US) Hub Programs The Director...Hub Programs will provide strategic input, and manage the development and deployment of Hub programs in the United-States,… more
- Merck & Co. (Millsboro, DE)
- Job DescriptionAssociate Director , Animal ServicesAbout the JobAnimal Health in Millsboro Delaware seeks to add an Attending Veterinarian in the role of Associate ... Director .This position will have overall responsibility for oversight and...other information as needed for annual reports to Federal regulatory agencies. Leadership for internal and external regulatory… more
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