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Interns will assist the Global Regulatory Affairs Oncology Liaison team with projects to support department goals and objectives. Intern Regulatory Affairs, Oncology. Interns will assist with development and submission of regulatory documents such as clinical study reports, study protocols and protocol amendments, and assist with activities in preparation for annual reporting requirements (e.g., Investigator Brochure, Orphan Annual report, etc.
$55 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The CMC Regulatory Affairs Sr. Manager at Gilead is responsible for providing strategic direction, operational support, and technical expertise for. Initiates process improvements and contributes to global process improvements, which have a significant impact for the Regulatory Affairs CMC Department or development matrix teams.
$199,320 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Collaborate and work cross-functionally with Manufacturing, Regulatory Affairs, Assay Development, Finance, and Quality functions to ensure all activities are scheduled and executed on time in accordance with program timelines.
$225,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Minimum of 5-7 years of experience in government affairs, lobbying, or a related role, with a strong understanding of the legislative and regulatory process. Carry out advocacy strategies to influence policies that impact pediatric rare disease patients and Soleno in collaboration with government affairs consultants.
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Author/review and/or coach team members to author CMC regulatory sections of IND/INDa. Contribute to regulatory strategies and support associated agency interactions and product-related inspections.
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Active Assisted Living Manager, RCFE or Healthcare Administrator license in accordance with state regulatory requirements. Knowledge of federal, state and local regulatory requirements as they relate to licensed Assisted Living & Memory Care communities and the ability to lead & operate within these guidelines.
$155,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Ensure compliance with industry standards and regulatory requirements (e.g., PCI-DSS, GDPR) We are looking for a highly technical Sr. Network Engineer who can lead people and projects to join our driven NetOps team.
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The Director, Regulatory Affairs will be responsible for developing and implementing global regulatory strategies encompassing clinical, non-clinical and CMC disciplines in support of investigational studies.
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Provide support in production or validation of summary tables, data listings and graphs required for trial report and clinical development, and CDISC data sets for regulatory submission. This position will be responsible for leading the programming aspect of a project for all programming deliverables from the single study through to regulatory approval.
$175,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Palo Alto has also served as an incubator and was headquarters to several other prominent high-technology companies such as Apple, Google, Facebook, Logitech, Intuit, Pinterest, and PayPal. Explore Palo Alto Veterans Affairs Palo Alto Health Care System (VAPAHCS) VAPAHCS is a teaching hospital associated with the Stanford University School of Medicine.
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To Clinical, Manager, Monitoring, Operations, Regulatory Affairs, Project Management, Healthcare. Works cross-functionally with other Guardant Health departments (such as Bioinformatics, Clinical Operations, Regulatory Affairs, Client Services, etc.
$154,900 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Work collaboratively with Manufacturing, QA and Regulatory to support CMC analytical deliverables. Author and revise SOPs, deviations, CRs and LIRs. Areas of responsibility include but are not limited to testing samples for Appearance, pH, UV and water content, HPLC, ELISA, western blot and SDS-PAGE as needed.
$35 - $37 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Sr. Director, Clinical Development will work closely with individuals in other functional areas (e.g., clinical operations, regulatory, preclinical, project management, quality, CMC, etc.
$315,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Vice President, Regulatory Affairs and Quality Assurance, will lead the regulatory and quality functions for all development-stage programs. Lead global regulatory strategy development for small-molecule product candidates in oncology and obesity.
$325,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Knowledge of local, state and federal regulatory requirements related to areas of functional responsibility Knowledge of principles and practices of organization, administration, fiscal and personnel management Knowledge of radiation production, positioning and radiation safety.
$66.46 - $88.05 an hourFull-timeExpandApply NowActive JobUpdated Today
regulatory affairs jobs Title: sr in Palo Alto, CA
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