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Senior Director, Franchise Health Economics And Market Access - Robotics, Endomech And Energy Platfo
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The Senior Director serves as a member and contributor to various business unit teams, providing functional expertise and leadership, and actively contribute to the business as a whole; Cross functional partners, including R&D, GSM, US marketing, Business Development, Medical Affairs, Clinical Research, Regional HEMA & Marketing, Regulatory Affairs, HCC and Legal.
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The Senior Power Resources Specialist will be responsible for overseeing a variety of regulatory compliance filings, engaging in complex electric regulatory proceedings, collaborating closely with external partners, and/or effectively advocating for SJCE’s interests at the CPUC, the CEC, and/or the CAISO.
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Intel's Legal, Trade, and Government Affairs (LTG) group offers unique opportunities to work in a variety of areas, including counsel to Intel businesses; technology and intellectual property licensing; patent prosecution; trademarks and brands; litigation, mergers, acquisitions and investing; public policy, legislative and regulatory lobbying; global trade, export, import, and customs; and corporate compliance.
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We seek outstanding candidates with teaching experience in the following: industry experience in entrepreneurship, drug/ medical device development, data science, regulatory affairs, clinical and medical affairs, quality management, project management, finance, business operations, research and development, biometrics, health economics and outcomes research or manufacturing.
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Verona Pharma is currently recruiting a Respiratory Sales Specialist to join our team, reporting to the Regional Sales Director. Communicate frequently with other Respiratory Sales Specialists across the country and cross-functional counterparts such as Marketing, Sales Ops, Market Access, Field Reimbursement, Training, and Medical Affairs to create alignment of business plan, focus on strategic drivers, and sharing best practices.
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The Environmental Compliance Specialist will play a key role in the maintenance and improvement of company-wide EMS; proactively monitors the various elements of the EMS to ensure compliance with internal systems, regulatory requirements, and applicable standards.
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We are looking for a candidate with an exceptional ability to engage crossfunctionally with other teams including Microbiology, Software & Data Science, Hardware Engineering, Process Engineering, and Quality & Regulatory Affairs (QA/RA.
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In partnership with L1 team members, designs and drives execution of medical affairs-related strategic goals and objectives, in keeping with overall company strategyFacilitates adherence to US regulatory requirements and International Conference of Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human use (ICH), pharmacovigilance and Good Clinical Practice (GCP) guidelines through the development and maintenance of applicable Company Standard Operating Procedures.
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ADARs will also be required to coordinate and communicate cross-functionally within NPC (e.g., Patient Support Center, Customer Engagement, Marketing, Market Access, Public Affairs, State & Government Affairs, Trade, Specialty Pharmacy Account Management, and other applicable third-party affiliates.
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Compliance: Ensure regulatory compliance with PCI-DSS, CJIS, and California Consumer Privacy Act of 2018 (AB-375) Security Certification(s), such as CISSP, CISM, CGEIT, GSEC, CEH, MCSE: Security, and CCNP-Security certification.
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Support coordination and implementation of global HTA strategies, including dossier development and submissions, in collaboration with Medical & Scientific Affairs and Market Access colleagues.
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In order to achieve these goals, the Education Specialist must collaborate with appropriate staff and district personnel, including but not limited to: Special Education Manager, Administration, DCP teachers, Central Office staff, School Psychologist, the Program Specialist, and other District/SELPA personnel.
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Certified Global Sanctions Specialist certification is a plus. Ability to create procedures to interpret and align with regulatory policies, while enabling investigators perform appropriate level of due diligence.
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PATH is currently seeking candidates passionate about making a positive impact on the lives of others to join our Coordinated Street Outreach Program serving San Diego as a Peer Support Specialist.
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Demonstrate a solid understanding of the appeals and grievance processes, including all regulatory and reporting requirements. Develop and manage reporting to monitor key performance indicators, identify trends, conduct root cause analysis, report to appropriate committees, and adhere to regulatory reporting requirements.
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regulatory affairs specialist jobs in Santa Clara, CA
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