• Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …well as other research areas centered around rare diseases and immune disorders.Summary The Manager / Senior Manager , Data Programmer is a member of the ... Management, as necessary.Participates in the development of and ensure compliance to Standard Operating Procedures (SOPs), policies, and guidelines.Remain informed… more
    HireLifeScience (06/05/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …organizations as well as US and global affiliates, learning their needs for compliance information and providing reporting support, as needed and as requested ... rare diseases and immune disorders. SummaryThis position will be part of the Compliance organization and will report directly to the Director, Compliance more
    HireLifeScience (05/04/24)
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  • Merck & Co. (Rahway, NJ)
    …Company's policies and procedures, quality standards and adverse event reporting -requirements internally and externally.The Clinical Research Manager (CRM) ... Job DescriptionPosition Description: Clinical Research Manager (CRM) - General Medicine (REMOTE) This role is primarily accountable for the end-to-end performance… more
    HireLifeScience (06/08/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …manages governance to ensure compliance , understanding and remediate gaps.- Ensures compliance with State and Federal reporting . Coordinates with Treasury on ... Summary This position is a key member of the Financial Disbursements team, reporting to the Head of Financial Disbursements, that manages the day-to-day Financial… more
    HireLifeScience (06/07/24)
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  • Novo Nordisk Inc. (Durham, NC)
    …well as internal stakeholders for the success of the Site. Relationships Manager , FUSE. Essential Functions Ensures all safety & environmental requirements and ... level of accountability for results and how the measurement process works Drive compliance of ISO5000 requirements Lead and support implementation of upgrades & new… more
    HireLifeScience (06/05/24)
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  • Novo Nordisk Inc. (Raleigh, NC)
    …with superior ability to lead through change. Relationships Internally, the Educator Manager (EM) reports to a Region Business Director (RBD) in the Commercial ... and utilize education and other relevant treatment guidelines to recommend, in compliance , the most appropriate NNI products and solutions Collaborate at a high… more
    HireLifeScience (06/04/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …considered for all Medical Affairs programs. Interact with legal and compliance as required. Proactively collaborate with other GxP quality representatives and ... Support continuous process improvement, interpretation of regulations, quality and compliance with regulations and company standards, policies and procedures through… more
    HireLifeScience (06/01/24)
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  • Novo Nordisk Inc. (Atlanta, GA)
    …co-promotion partners, associations, and field and home office personnel. Essential Functions Compliance : Adhere to the Prescription Drug Marketing Act of 1987 and ... of Motor Vehicle Records. Development of People Ensure that reporting personnel have individual development plans (IDP), with annual...and aspiration plans and are in place for all reporting personnel to enable the achievement of goals and… more
    HireLifeScience (06/06/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …areas centered around rare diseases and immune disorders. Summary The Regulatory Data Manager will be a key member of the Global Regulatory Affairs (GRA) Process ... Excellence function, responsible for driving data governance, reporting , and analytics for RA. This will include working within and optimizing the defined, R&D data… more
    HireLifeScience (05/05/24)
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  • Daiichi Sankyo, Inc. (Atlanta, GA)
    …centered around rare diseases and immune disorders. Summary: The Oncology Territory Manager represents Daiichi Sankyo to assigned customers. The Oncology Territory ... Manager represents the assigned product, and its approved indications,...group settings.Meet all administrative expectations and standards, including budgets, reporting , and communication.Maintains a current key customer target list,… more
    HireLifeScience (05/31/24)
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  • Lundbeck (Dallas, TX)
    …lead the way in creating positive customer experiences!As a BioPharmaceuticals Account Manager , you lead the promotion of our infusion product, driving demand ... patients including the full range of treatment options available. Pharmaceutical Environment/ Compliance - Ability to apply knowledge of pharmaceutical and regulatory… more
    HireLifeScience (06/05/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …myeloma. Legend Biotech is seeking an Associate Director for Operations Compliance and Investigations Managementas part of the Technical Operations team based ... in Raritan, NJ. Role Overview The Associate Director for Operations Compliance and Investigations Management will provide strategic direction and leadership for the… more
    HireLifeScience (04/19/24)
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  • Lovelace Biomedical Research Institute (Albuquerque, NM)
    …federal contracting process to include both pre- and post-award management and compliance reporting . Will perform contract and subcontract administration in ... the Director of Research Administration and under limited direction, the Contracts Manager - Federal Contracts and Compliance , will oversee end-to-end contract… more
    HireLifeScience (05/14/24)
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  • Merck & Co. (North Wales, PA)
    …Contracting and Distribution Strategies team in US Vaccines is seeking a Customer Manager who will be responsible for managing our contracts and agreements in the ... future contracts.Working with sales teams and customers to ensure appropriate compliance with the terms and conditions of our contracts.Collaborating with… more
    HireLifeScience (05/31/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …through outsourcing (eg, study startup, study conduct, study closeout, and reporting ).Provides oversight for Data Management CRO and other third party vendors ... to ensure compliance with the protocol, external/internal standards, Good Clinical Practices (GCPs), applicable regulatory guidelines, Policies, SOPs, and other… more
    HireLifeScience (06/06/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …and International Conference on Harmonization (ICH) guidelines.The Senior Clinical Study Manager will have routine interaction with key internal and external ... abroad, governmental, academic, community and industry organizations.The Senior Clinical Study Manager role is primarily a tactical study delivery role, reporting more
    HireLifeScience (05/22/24)
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  • Catalent (Harman, WV)
    The Manager , Supply Chain - Warehouse , reporting to the Director, Supply Chain, has an opportunity to make a significant impact on the way that the Harman's ... site operates. The Manager , Supply Chain - Warehouse will lead a shift...and Materials Services Associates. Responsibilities include: project participation, dashboarding, reporting , and governance. The scope includes all continuous improvement… more
    HireLifeScience (05/02/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …contracting agreements. In collaboration with the Associate Director, the Associate Manager will support CMR's partnership and alliance contract management strategy ... leadership, across all organizations within CMR as well as Procurement, Legal, Compliance , Privacy and other key focus areas. To support the successful planning… more
    HireLifeScience (05/22/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …Sponsored Studies (CSS) Support the preparation, set-up, and execution and reporting of all global oncology medical affairs operations clinical trial activities, ... company sponsored studies review and approvals are current and accurate.Liaison and reporting on study activities with other relevant GOMA functions and the Global… more
    HireLifeScience (05/22/24)
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  • Eisai, Inc (Nutley, NJ)
    …profile, we want to hear from you. Job Summary Oversees and assures compliance with standard operating procedures, compliance with regulatory standards and ... medical writing skillsKnowledge of International and US Regulations for reporting Adverse Events for Investigational and Marketed products.Minimum 5-7 years… more
    HireLifeScience (05/28/24)
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