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As a Regulatory Affairs Manager, you will play a pivotal role in leading a team of Project Managers and Specialists, obtaining, and maintaining marketing approvals for our products in the UK. Implementing the regulatory strategy for the UK. Ensuring full regulatory and company compliance, and provide regulatory expertise to support clinical research, product launches, and business development.
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The Associate Director, Immunology Medical Affairs Data Analytics will collaborate with colleagues across the Immunology US Medical Affairs organization, such as Medical Heads, MSL Field Directors, Integrated Evidence Team Leads, as well as data analysts in the business units with whom Medical Affairs collaborates: Commercial (Franchise and Brand), Global Medical Affairs, Janssen Scientific Affairs, and Strategy Analytics and Transformation.
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Within HPD’s Office of Legal Affairs, the Regulatory Affairs Division (RAD) provides legal support services for the Agency’s regulatory and enforcement functions and advice on compliance with external City, State, and Federal statutory and regulatory requirements.
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Master’s degree in engineering, business, education, counseling, psychology, student affairs, or related field. Bachelor’s degree in engineering, business, education, counseling, psychology, student affairs, or related field plus two (2) years of related experience working with students in a 1:1 setting.
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The Regional Medical Scientific Director (Medical Science Liaison) is a credentialed (i.e., PhD, PharmD, DNP, MD) Director Level Medical Affairs position and therapeutic and disease expert who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs.
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Represent Planned Parenthood in Nebraska at events, internal and external task forces, coalitions, workgroups, as approved by the Senior Manager of Public Affairs and Advocacy Strategists. Support the Public Affairs team by monitoring and tracking relevant state and federal legislation.
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Experience working with regulatory compliance requirements such as HIPAA, HITRUST, SOC2, PCI, etc. Partner with the Chief Information Security Officer (CISO) to set department vision and direction aligned with security leadership and key business partners.
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Experience working within regulatory standards and requirements such as SOX, HIPAA, GDPR, HITRUST is preferred. The candidate will also leverage AGILE project management skills to drive improvements in IAM services and processes to improve the overall security posture.
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GEICO's Government and Regulatory Affairs team is looking for experienced Government Relations individuals to join our team to advance the Company's legislative and regulatory agenda.
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To fulfill these duties, you will collaborate with internal project teams such as transmission and renewable development, engineering, government affairs, and construction management; external teams like environmental and engineering consultants, and external legal counsel; and external stakeholders such as private landowners, state/federal resource agencies, and conservation organizations.
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As a member of a cross-functional team, GRAIL's Principal Scientist, RWE will build and maintain cross-functional relationships with Medical Affairs, Clinical Development, Regulatory, and business teams; and collaborate with the team effectively to ensure the implementation of rigorous methods and delivery of scientifically sound results, in support of regulatory submissions, publications and/or other uses.
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Able to evaluate the environmental permitting, regulatory, and compliance aspects of project. Identify key gaps / needs as it relates to environmental permitting, regulatory, and compliance aspects of project.
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A. Degree: Community planning; or related field such as urban affairs, architecture, landscape architecture, engineering, sociology, geography, economics, political science, or public administration that included at least 12 semester hours in the planning process, socioeconomic and physical elements of planning, urban and regional economic analysis, and development finance.
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Experience in change management processes, manufacturing operations, quality operations, and/or regulatory affairs. The QA Manager/TL is accountable for ensuring cGMP compliance within the site's B1 Biological ABI/BPM/ Pharmaceutical and Pharma/Biopackaging Operations, is expected to identify and escalate areas of risk, provide guidance and support in the interpretation and enforcement of regulatory guidelines, and support site project initiatives.
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Serve as corporate level data security and compliance subject-matter expert, advising on compliance with contractual data security obligations under applicable federal, state and foreign legislation, including technical compliance with FISMA, NIST and other regulatory/legal information security requirements (e.g., FERPA, HIPAA, Privacy Act.
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regulatory affairs jobs Title: regulatory affairs project Company: Jobget in Lincoln, NE
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