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In-depth knowledge of CMC regulatory requirements for Advanced Therapy Medicinal Products and have an understanding of current global and regional trends in CMC Regulatory Affairs for such products.
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Mammoth is hiring a Director/Sr. Director, Regulatory Affairs, Therapeutics, to lead the regulatory activities of our growing CRISPR-based therapeutic programs as we bring them from concept to market.
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Reports to: Global Regulatory Affairs Director. This Senior Regulatory Affairs Specialist will have an opportunity to work on new to market technology that is improving the field of diagnostic imaging and saving patient lives.
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Allogene is seeking a Senior Director, CMC Regulatory Affairs to provide support for products under development and lead CMC product strategy and provide regulatory direction to quality, manufacturing/tech ops and supply chain teams.
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We invested in new offices, sector teams and practice groups including investor engagement; shareholder activism; governance; regulatory and public affairs, including geopolitical; crisis; litigation; social issues including climate change and diversity, equity and inclusion; cybersecurity, data and privacy; employee engagement; digital communications; opinion research and analysis, and; creative services.
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6+ years of legal experience, including government, in-house and/or law firm experience advising technology companies, including demonstrated work experience in the area of trust & safety and regulatory affairs.
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Practical experience in the pharmaceutical or biotech industry of at least five years in at least one major area of drug development, such as Discovery, Preclinical Development, Clinical Development, or Regulatory Affairs.
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The Director of Medical Affairs at Thermo Fisher Scientific will play a pivotal role in both strategically and functionally leading the North American (NA) Medical Affairs Team, undertaking the initiatives supporting the Clinical Sequencing Division (CSD) activities.
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These will include leadership of our work in media/PR, corporate branding, executive visibility and thought leadership, scientific communications, patient advocacy, public affairs with strong collaboration on investor relations as well as government and public affairs over time.
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We are looking for a regulatory specialist and permitting lead to support our clients in central and northern California. Work will include managing regulatory complexities and permitting for a range of projects, from municipal projects to large infrastructure programs, working with multidisciplinary teams of specialists, and performing both office and field work.
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The Scientific Director or Medical Director in Medical Affairs is responsible for the actively participating in or driving post-marketing medical planning & execution of assigned medical affairs activities at BeiGene - Americas.
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We are seeking an experienced VP of Communications / External Affairs to build a communications strategy that highlights insitro's ground breaking science and how computational approaches can make a profound impact on drug discovery and development of new medicines for patients in need.
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In the position of Clinical Research Program Manager, you work under the supervision of the Director, and are responsible for overseeing study day-to-day activities, progress, and regulatory affairs.
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Experience with clinical trials regulatory affairs, or related clinical trials experience such clinical research coordinator experience. Ensure that all investigators maintain the proper credentials and maintain these records in central regulatory binder (e.g. medical licenses, CVs, GCP/HSP certifications, NCI CTEP registration, SIP accounts, etc.
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Works collaboratively with vendors, Clinical Research, Drug Safety, Regulatory Affairs, Clinical Operation, and Project Management teams to meet project deliverables and timelines for statistical data analysis and reporting.
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regulatory affairs jobs Title: sr director Company: Abbott Laboratories in San Francisco, CA
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