• Insmed Incorporated (Bridgewater, NJ)
    …Best Workplaces in New York™, and Best Workplaces for Millennials™ lists.OverviewThe Manager , Regulatory Operations will be responsible for functional ... or existing systems in Regulatory AffairsRequired Skills5 years of Regulatory Operations experienceExtensive knowledge and experience with Microsoft Office,… more
    HireLifeScience (04/10/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …coordinate, and review US regulatory submissions in collaboration with USRL, Regulatory Operations (RO), and other key stakeholders (eg Protocol Amendments, ... areas centered around rare diseases and immune disorders. Summary The Manager , Regulatory Affairs - Regulatory Project Management (RPM) provides planning… more
    HireLifeScience (05/26/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …well as other research 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...as cross-functional stakeholders (eg, RA CMC, R&D Excellence, Clinical Operations , IT).Responsibilities Operate within and in support of the… more
    HireLifeScience (05/05/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …preferred- 1 or More Years Strong appreciation of the impact of regulatory bodies on pharmaceutical operations . preferred- Experience auditing software vendors ... Non-GxP activities, assuring that these systems are compliant with global regulatory and Daiichi Sankyo requirements, and business expectations. Executes the Global… more
    HireLifeScience (06/05/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …around rare diseases and immune disorders.Summary The Clinical Trial Information Disclosure Manager leads company operational activities to comply with US, EU, Japan ... A member of the Global Clinical Trial Disclosure Platform and Operations Committee. Facilitates the company's compliance with current disclosure requirements and… more
    HireLifeScience (06/07/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …and cultures. Additionally, this position possesses a working knowledge of clinical operations and relevant regulatory requirements. This position has experience ... the protocol, external/internal standards, Good Clinical Practices (GCPs), applicable regulatory guidelines, Policies, SOPs, and other relevant guidelines.Ensures Data… more
    HireLifeScience (06/06/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …opportunity employer including veterans and people with disabilities. Summary The Manager External Data Management, is accountable for an end-to-end delivery of ... for clinical trials, companion diagnostics trials, clinical development, and regulatory submissions. The position will perform validation of the electronically… more
    HireLifeScience (04/28/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …research areas centered around rare diseases and immune disorders. Summary The Manager , Global Clinical Operations (GCO) Functional Excellence (FxExc), will help ... needed, help support the partnership with Clinical Trial Business Operations (CTBO)to:-monitor GCO processes and workstream implementations for effectiveness.-monitor… more
    HireLifeScience (04/28/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …as other research areas centered around rare diseases and immune disorders.Summary The Manager of Data Governance Stewardship will work in areas required for the ... with and understanding of key industry best practices as well as legislative, regulatory and industry artifacts / frameworks, such as, the following: o 21 CRF… more
    HireLifeScience (04/12/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionPosition Description: Clinical Research Manager (CRM) - General Medicine (REMOTE) This role is primarily accountable for the end-to-end performance ... standards and adverse event reporting-requirements internally and externally.The Clinical Research Manager (CRM) could be responsible for a particular study for… more
    HireLifeScience (06/08/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …Value process in evaluating study budgetsCollect information and coordinate with DS Regulatory Operations to post trial information on required public forums ... under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations , in adherence to the protocol, Good Clinical Practices… more
    HireLifeScience (06/06/24)
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  • Insmed Incorporated (Bridgewater, NJ)
    …Workplaces in New York™, and Best Workplaces for Millennials™ lists.OverviewThe Manager , Laboratory operations will manage the internal analytical laboratory ... characterization for drug substance, drug product and reference standards. The Manager must possess a good understanding of pharmaceutical development processes from… more
    HireLifeScience (05/28/24)
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  • Merck & Co. (Rahway, NJ)
    …TA Head and CRD as needed.Works in partnership with GCTO country operations , finance, regulatory affairs,-pharmacovigilance, legal and regional operations , ... assigned protocols and sites in a-country.-Under the oversight of the CRA manager the person ensures compliance of study conduct with-ICH/GCP and country… more
    HireLifeScience (06/05/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …in the treatment of multiple myeloma. Legend Biotech is seeking a Project Manager , Process Engineer- Consultant as part of the Global MSAT team based in ... effort will have a focus related to industry available cell therapy unit operations to be incorporated with an automation platform that integrates with MES systems… more
    HireLifeScience (06/04/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …in the treatment of multiple myeloma. Legend Biotech is seeking QA Manufacturing Excellence Manager as part of the Quality team based in Raritan, NJ. Role Overview ... The QA Manufacturing Excellence Manager role is an exempt level position with responsibilities...environment. This role will also provide oversight of technical operations activities including data or document review, risk assessments,… more
    HireLifeScience (04/25/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …of multiple myeloma. Legend Biotech is seeking an Associate Director for Operations Compliance and Investigations Managementas part of the Technical Operations ... based in Raritan, NJ. Role Overview The Associate Director for Operations Compliance and Investigations Management will provide strategic direction and leadership… more
    HireLifeScience (04/19/24)
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  • Eisai, Inc (Nutley, NJ)
    …to standards.Oversee regional security vendors.Prioritize risk-based reduction efforts. Manager investigations.General Compliance Activities:Maintain an inventory of ... play a pivotal role in ensuring the organization's adherence to security, regulatory , and compliance standards. Collaborating with business and EIT stakeholders, you… more
    HireLifeScience (05/28/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …or material handling tasks in a backup role, as needed. Updates supervisor/ manager of work status or problems with recommendations for improvement or correction. ... decision making and troubleshooting skills in relation to procedures, regulatory standards, and company policies. Ensure non-conformances are investigated thoroughly… more
    HireLifeScience (03/13/24)
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  • Program Manager , Integrity…

    Meta (New York, NY)
    …inquiries and investigations across a large XFN team. **Required Skills:** Program Manager , Integrity Regulatory Operations Responsibilities: 1. Co-ordinate ... **Summary:** Integrity Regulatory Operations team works cross-functionally to...manager to join our team and lead our regulatory compliance efforts in the integrity space. In this… more
    Meta (04/26/24)
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  • Regulatory Operations Manager

    Publicis Groupe (New York, NY)
    …trades, or just an all-around nice person, let's chat. **Job Description** The Manager , Regulatory Review is responsible for ensuring regulatory submissions ... to PM and Account teams as they prepare projects for Medical Legal Regulatory (MLR) review + Submit completed materials to the client, both electronically and/or… more
    Publicis Groupe (05/10/24)
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