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The Regulatory Affairs Specialist supports the oversight of regulatory matters and strategy implementation to ensure the organization complies with applicable regulations. Regulatory Affairs Specialist.
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Preferred Qualifications Experience working with legal counsel on regulatory and legislative affairs. The Virtual Power Plant Policy Director will lead SUN’s policy, regulatory, and advocacy efforts to implement solar + batteries Virtual Power Plant (VPP) policy across the country and in targeted states.
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Transamerica is organized by lines of business (Life Insurance, Annuities, Mutual Funds, Retirement Plans, and Employee Benefits), which are supported by Transamerica Corporate (Corporate Development; Finance; Internal Audit; Legislative, Regulatory & Policy; Office of the CEO; People and Places; Brand; Corporate Affairs; Risk; and Technology.
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Health and Work/Life Balance Benefits; Be Well Company sponsored holistic wellness program which includes Wellness Coaching and reward dollars, Parental Leave, Adoption Assistance, Employee Assistance Program, College Coach Program, Back-up Care Program, Paid Time Off to Volunteer, Employee Matching Gifts Program, Employee Resource Groups, Inclusion and Diversity Programs, Employee Recognition Program.
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The NCI/NCTN Senior Regulatory Affairs Start-Up Specialist is expected to resolve, with minimal supervision, regulatory queries, and participate in the initiation of the new study, as well as, communicate transition of the new study to the applicable team Regulatory Affairs Specialist post-site initiation.
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Currently seeking a new Global Director of Regulatory Affairs to help spearhead our client's 1st generation PMA submission as well as future supplements and OUS international registries for global commercialization.
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Collaborate with US Government Affairs team to identify and develop policy priorities related to commercial market access. Minimum of 10 years of experience in health policy, market access, and reimbursement, including comprehensive knowledge of commercial payment systems and the healthcare regulatory environment.
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Senior Director, Regulatory Affairs CMC. This position will be working across the company's mid-stage, new development pipeline and will be reporting into the VP of Regulatory Affairs.
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Minimum of 7 years of Regulatory Affairs experience; preferably using data, software, and services to enable processes, make decisions, and deliver value. Ability to clearly explain and articulate the value of relevant data/content, such as Pharmacovigilance, Chemical Manufacturing Controls, and Regulatory Intelligence.
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This position requires an aplished candidate with strong academic credentials, political acumen, relationships with state Department of Insurance officials and state legislative officials and staff, as well as a developed technical background in regulatory and legislative matters for all lines of property and casualty insurance (P&C), including workers'pensation.
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Youve got at least four years experience in the Life Sciences R&D industry in at least one of the following areas: research, clinical development / operations, pharmacovigilance, regulatory, medical affairs, medtech, patient services, MD&D (medical device and diagnostics) or related areas (CROs), health institutions, health technology companies, etc.
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The Pharmaceutical Regulatory Affairs Senior Manager will use their experience and knowledge in pharmaceutical industry regulatory affairs to lead and manage complex projects for our clients in the pharmaceutical sector, and provide strategic advice, guidance, and solutions on regulatory matters.
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A minimum of 8 years of prior pharmaceutical/biotechnology industry experience, including at least 6 years in regulatory affairs, is required. They have retained us to assist them in their search for a Director of Regulatory Affairs.
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The Director, Regulatory Affairs is responsible for assisting with establishing and managing regulatory strategies, life cycle plans, and pre/post regulatory approvals. Establish regulatory strategies and process by collaborating and coordinating with relevant development and CMC team members.
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The Senior Medical Writer is a writing-based position within our Global Regulatory Affairs department. Authors deliverables with consideration for regulatory, corporate, departmental, and quality standards (documents include but are not limited to protocols, clinical study reports, Investigator's Brochures [IBs], annual reports, HA briefing packages and response documents, submission summary modules, and integrated data summary reports.
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regulatory affairs jobs in Philadelphia, ID, Maine
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