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Experience working with Food and Drug Administration (FDA), International Council on Harmonisation (ICH) guidelines, cGMPs and SOPs regulatory rules, regulations and guidelines. Operates general analytical instruments during raw material, IP and FP testing such as High Pressure Liquid Chromatography (HPLC), Ultra Performance Liquid Chromatography (UPLC), Gas Chromatography (GC), Ultra Violet visible spectroscopy (UV/Vis), automatic titration, Infra-Red Spectroscopy (IR), Malvern Mastersizer, Thin Layer Chromatography (TLC) and dissolution apparatus (Distek); Creates and uses custom fields in Empower software while operating HPLC/UPLC and GC instruments.
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The Associate Director, Market Access Contracting role is to work cross-functionally with internal and external stakeholders to support the execution of channel Strategy, documenting contractual relationships that support US Market Access strategy, protocols and operations to ensure an efficient and compliant organization.
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We are seeking a dedicated Associate Research Scientist to join our early translational group in Lawrenceville, NJ. In this role, you will support programs transitioning from discovery to First-in-Human (FIH) studies, running various experiments under the guidance of senior scientists.
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IMMEDIATE NEED for Sr. Manager of Clinical Trial Inspection Readiness to join multi-billion dollar client and leading pharmaceutical company! The Sr Manager, Clinical Trial Inspection Readiness, is responsible for leading clinical inspection readiness activities to support the Program Operations Leader and Clinical Study Lead(s) for one or more assigned clinical programs within Clinical Trial Management.
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Lead coordination and filing of N.A. Government Affairs Department’s U.S. Lobbying Disclosure Act reporting. This position, reporting directly to the Vice President, Global Government Affairs, is responsible for supporting the development of N.A. government and public affairs strategies, while working as an effective liaison with teams and colleagues in the Syensqo business units and functions to ensure a streamlined and coordinated approach.
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Position : Sr Databricks Architect. Sr Databricks Architect. Write and optimize Apache Spark code in Scala, Python, or other supported languages. Analyze business requirements and design efficient and scalable data processing solutions using Databricks.
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Serves as a modeling and simulation (M&S) representative on project teams interacting with clinical, pre-clinical, biostatistics, and regulatory agents, as well as CROs. Interact with the asset development team to support the design and interpretation of Clinical Pharmacology and pharmacometrics studies, to prepare the regulatory dossier and respond to reviewer queries.
$121,000 - $197,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Cranbury Animal Hospital is searching for a talented and dedicated veterinarian to join our close-knit team.
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The Corporate Underwriting Associate will be a critical member of the central underwriting organization, Corporate Underwriting, responsible for the oversight and steering of our portfolio. For more information on MRSI, including licensing, regulatory-required, and other information on the operating companies, visit.
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Rocket is seeking an Associate Director, Regulatory Operations to support the development and implementation of the global regulatory strategy of Rocket’s gene therapy programs in accordance with regulations and through collaboration with external partners, internal cross‑functional teams, and global health authorities.
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Treasury Senior Associate in AIS Middle Office providing hedge funds with fund administration. Ensure self and team complies with risk, regulation and compliance programs and applicable laws and regulatory requirements.
$50,000 - $83,750 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Senior Associate Brand Manager, International Marketing role is a critical part of the International team and will be responsible for contributing to the development of the Waterpik international brand strategy, working to identify and accelerate global new product launch opportunities and for overseeing elements of global brand equity on the Waterpik brand.
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The Sr. HRIS Analyst, Talent and Recruiting is responsible for analyzing, designing, configuring, testing, and deploying Workday HR solutions to meet the business requirements of clients. The Sr. HRIS Analyst, Talent and Recruiting is responsible for analyzing, designing, configuring, testing, and deploying Workday HR solutions to meet the business requirements of clients.
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For the Consulting Associate, Engineer position, we anticipate the annual base pay of $62,000 – $72,422 USD. An employee’s pay position within this range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, geographic location, performance, shift, travel requirements, sales or revenue-based metrics, and business or organizational needs.
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The Study Associate (SA) I is responsible for operational study support during study start-up, maintenance, and close-out. Monitors Trial Master File related KPIs and performs quality review of the eTMF (per CRO oversight plan) while collaborating with internal and CRO study teams to resolve any issues and risks.
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Title: sr regulatory affairs associate Company: Thermo Fisher Scientific in Princeton, NJ
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