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Why You Should Apply:Lead regulatory affairs for groundbreaking stem cell therapies in neurodegenerative diseases. Leadership and Mentorship: Build and lead a high-performing regulatory affairs team, providing mentorship and fostering a culture of compliance and continuous improvement.
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Work closely with Field Medical, Global Medical Affairs, Commercial, and other cross-functional teams to ensure the alignment of educational initiatives and engagement strategies with objectives and KOL knowledge needs.
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Vice President/Senior Vice President, Regulatory Affairs. You will provide regulatory leadership and provide strategic direction to Regulatory Affairs, Clinical Quality, Medical Writing departments and lead Regulatory Affairs group, including hiring, mentoring, and leading staff.
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Serve as the Medical Affairs lead for strategic partnerships. Provide strategic and scientific leadership to and define global medical affairs strategyfor early-stage clinical programs. Liaise with global and regional medical affairs to ensure medical insights from all keymarkets are integrated into and inform product development.
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Actively collaborate with Senior Management and Enterprise functions (e.g. Clinical, Commercial, Medical Affairs, amongst others) to provide regional regulatory insight and broader drug development expertise.
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You’re the right fit if you have the following:You acquired a minimum of 5 years’ experience in regulatory affairs within the FDA regulated, global medical device industry. JOB DESCRIPTION Job TitleRegulatory Affairs Program ManagerJob DescriptionAs a Regulatory Affairs Program Manager, you will be an important member of the Philips Regulatory Affairs Centralized Services Team, committed to improving billions of lives worldwide.
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Senior Medical Director / VP – Neurology Medical Affairs with the leading RNA company. As the Senior Medical Director/ VP– Neurology you will play a key role in growing the company, building out the medical affairs team and leading the neurology portfolio.
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As an Associate Director, Global Regulatory Affairs Marketed Products you will define, develop and lead global strategies to maximize global regulatory success towards achievement of program objectives for complex and/or multiple projects.
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Work with the Consul General and Deputy Consul General to ensure that the Consulate’s press, politics and public affairs work is planned, coordinated with all the other sections in the Consulate and delivered in line with key objectives.
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Minimum of 15 years of experience in regulatory affairs within the biotech or pharmaceutical industry, with at least 8 years in a senior leadership role. Scienta Search is seeking a seasoned and strategic leader to join our executive team as the Global Vice President of Regulatory Affairs.
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Responsible for the development and planning, organization and direction of programs, policies and activities of the Fiscal Affairs office, Bursar, Business Office, and Financial Aid. Responsible for supervision of the college budget.
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Syndax has an exciting new opportunity for an Associate Director, Regulatory Affairs. Syndax Pharmaceuticals is looking for an Associate Director, Regulatory Affairs. Independently directs as well as prepares global regulatory affairs strategies and executes regulatory activities for Syndax, with general guidance from manager and regulatory affairs leadership.
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Demonstrates acceptable skills with increasing independence in the area of regulatory strategy such as understanding broad concepts within regulatory affairs and implications across the organization and globally; proactively identifies regulatory issues; offers creative solutions and strategies, including risk mitigation strategies.
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As part of the Consulting leadership team, the Managing Director - Medical Affairs will contribute to setting business direction, strategy, and priorities and take ownership for driving the overall growth and scalability of the Medical Affairs consulting business.
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Responsible for the management and leadership of Regulatory Affairs including Reg Strategy, Reg CMC, Reg Ops, Advertising and Promotion and Labeling. The VP, Head of Regulatory Affairs is a key leader accountable for the development and execution of comprehensive global regulatory strategies for the development programs and marketed products at Innoviva Specialty Therapeutics.
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Title: affairs Company: Turnstone Biologics in Charlestown, MA
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