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The Manager of Regulatory Affairs at AES Clean Energy (AESCE) will be tasked with supervising AESCE's positions and fostering relationships within the Federal Energy Regulatory Commission (FERC), managing policy positions within Regional and Independent Transmission Organizations (RTO/ISO), and taking the lead on filings and policy positions at state Public Utility Commissions (PUC) or Public Service Commissions (PSC) in key states.
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Reporting to the CEO the SVP/VP Global Regulatory Affairs drives the articulation and. In the short-to-mid term the SVP/VP Global Regulatory Affairs primary focus shall be the.
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Collaborate with the Project Management and CMC teams and related functions, including discovery, non-clinical development, Formulation, Analytical Development, QA, and CMC Regulatory Affairs.
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Represent PCDS at team meetings and coordinate between PCDS and other functions including CMC, Regulatory Affairs, Clinical Operations, and Platform and Discovery Sciences. The candidate should possess an in-depth understanding of safety pharmacology, investigative and regulatory toxicology, and have experience designing and critically evaluating results of exploratory and GLP-compliant toxicology studies.
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The primary purpose of this position is: To serve as a Public Affairs Specialist, to carry out a wide range of public affairs assignments that include elements of media operations, social media, community engagement, command information, visual information, communication planning, contingency/crisis response, special event planning, environmental, and security.
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Serve as a student conduct hearing officer as needed by the Associate Vice President for Student Affairs. Participate in the administrator on-call weekly rotation with the Associate Vice President for Student Affairs, Director of Residence Life, and other administrators.
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Director, Safety, Regulatory and Medical Affairs Quality Standards is responsible for the management of a RDQA global Safety, Regulatory Affairs (RA) and Medical Affairs (MA) QA team which provides independent quality oversight of GxP activities, covering the AbbVie drug, device and cosmetic portfolio.
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Draft and oversee the DMPK/clinical pharmacology sections of regulatory communication documents, such as briefing documents for regulatory meetings, Investigator Brochures (IBs), Pediatric Investigational Plans (PIPs), and reports on population pharmacokinetics (popPK) modeling/simulation.
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Monitors projects for regulatory compliance and maintains knowledge of the latest developments in the utility industry, to meet North American Electric Reliability Council ( NERC ), Federal Energy RegulatoryCommission ( FERC ), Electric Reliability Council of Texas ( ERCOT ) and Texas Public Utility Commission (TX.
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Knowledge of utility standards and regulatory requirements, to meet North American Electric Reliability Council ( NERC ), Federal Energy Regulatory Commission ( FERC ), Electric Reliability Council of Texas ( ERCOT ) and Texas Public Utility Commission (TX.
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The clinical trial responsibilities will include supervising study monitors and working closely with the Project Manager, VP of Regulatory and Quality Affairs, Chief Technology Officer, and Senior Director of R&Dto ensure clinical trial milestones are achieved on time and within budget.
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Our suborganizations vary in nature, and include: Human Resources, Training & Development, Safety & Security, Government Affairs, Public Affairs, Community Services, Transportation (Marine, Aviation, etc.
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Veteran’s Affairs and Institutions C-Suite, Staff psychiatrists, attendings, staff and in-house pharmacy, Director of Nursing, Outpatient and Inpatient Psych Program Directors. Sales Leadership, Sales Operations, Marketing, Market Access (RAM’s), Medical Affairs, Finance, HR, Field Reimbursement and Compliance.
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60367 Director, Regulatory Compliance $158K - $244K, Purchase, NY. 60371 Chief Regulatory Officer (Remote Anywhere USA) 60372 VP, Compliance (Remote Anywhere USA) 60330 Director Legal (Remote Anywhere USA), San Antonio, TX.
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Over 15 years of progressive advancement within global regulatory affairs in the pharmaceutical /biotech industry. The Vice President, Regulatory Affairs & Quality is in charge of providing subject matter expertise on all matters related to FDA and global regulatory requirements, as well as leading the growth and responsibilities of the regulatory and quality department.
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regulatory affairs jobs Company: Aegon Asset Management in Oklahoma
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