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5+ years experience in Communications, Public Relations, Public Affairs. We're looking for an experienced professional with experience in media training, external speaking, and content development (i.e. op-eds, keynote presentations, videos, bylines), as well as a deep interest in AI and how it will impact business, public policy, and culture.
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Meet is partnering with a late stage pediatric rare disease startup looking for a high-level Regulatory Affairs professional to join their team. This position will be reporting into the SVP of Regulatory Affairs and will be supporting Clinical Regulatory and Regulatory CMC functions.
$240,000 - $280,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Ensure compliance with relevant regulatory requirements and industry standards (e.g., GDPR, CCPA, PCI-DSS). Strong understanding of regulatory requirements and industry standards (e.g., GDPR, CCPA, PCI-DSS.
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For the health and safety of our team members and residents, Oakmont Management Group may require team members to vaccinate, participate in daily screening, surveillance testing, and to wear face coverings and other personal protective equipment (PPE) to prevent the spread of the COVID-19 or other communicable diseases, per regulatory guidelines.
$90,000 - $92,000ExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Familiarity with data protection laws, including GDPR, CCPA, and HIPAA.Experience in incident response, risk management, and regulatory compliance in the cybersecurity domain. Regulatory Compliance: Monitor and interpret information security and cybersecurity regulations, and other relevant laws.
$214,500 - $321,700ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Job Description: Rakuten International oversees 7 businesses with over 4,000 employees globally.
$200ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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This investigation includes but is not limited to a criminal, civil litigations and regulatory review, employment, education, and credit review (role dependent). We assist companies and non-profit organizations in delivering benefits to their employees.
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In this role, you will partner with our global Accounting, Finance, Financial Systems, Regulatory/Compliance Legal and Tax teams. To further this important mission, we are seeking a Treasury Accountant who has expertise in financial instrument hedging and investment valuation to support accounting for our internal Treasury initiatives.
$126,600 - $189,800Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Participate in meetings with regulatory agencies as medical program leader. Medical review of clinical documents submitted to regulatory agencies. Working with Clinical Research team and key personnel including Medical Directors, this highly skilled and team-oriented Medical Director will be a physician and will have subspecialty training in Nephrology or Infectious Disease or Rheumatology and have at least 5 years of clinical research and development experience.
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Willingly assists as needed in all peri-anesthesia settings including the preoperative area, PACU, and the Endoscopy PACU. · Maintains the principles of confidentiality and HIPPA. Understands the legal/regulatory requirements related to the release of information.
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Minimum of 7 years of experience in external affairs, advocacy, government relations, or related roles, preferably within the technology or financial services industry. Public Affairs: Represent &/or support others’ participation at events, conferences, and other forums to build relationships, foster awareness and trust in the platform and our team, and advance our programmatic and business goals.
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Liaise with functions such as Development, Manufacturing, Supply Chain, Project Management, QA, QC, and Regulatory Affairs as well as off-site functions such as external partners. We believe that our PCVs could receive regulatory approval based on successful completion of clinical studies utilizing well-defined surrogate immune endpoints, consistent with how other PCVs have obtained regulatory approval in the past, rather than requiring clinical field efficacy studies.
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Our client is looking for an energetic and talented Sr. Associate Engineer to contribute to the Polysaccharide Upstream Pilot Plant function within the CMC team. Sr. Associate Engineer, Polysaccharide Pilot Plant.
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This crucial role demands extensive expertise in the development and commercialization of small molecule pharmaceuticals, as well as a comprehensive understanding of regulatory requirements for rare disease therapeutics.
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The Computational Biology group in the Clinical Biomarkers & Diagnostics (CBD) department at is seeking a highly motivated Sr data scientist to join our team and contribute to develop machine learning modeling and prediction pipelines using multi-modal biomarker data from clinical trials.
$85 - $92ExpandApply NowActive JobUpdated Today
regulatory affairs jobs Title: sr Company: Csl Behring in Burlingame, CA
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