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Science & Biotech Online Resumes

Clinical Regulatory Affairs

Clinical Regulatory Affairs - 2 Years of Experience - Near 02120

Tags for this Online Resume: regulatory affairs, quality assurance, clinical regulatory affairs, eCTD, marketing authorization applications, Dossier submissions, FDA , QUALITY SPECIALIST

Clinical Regulatory Affairs - 20 Years of Experience - Near 08730

To be a part of organization that is positioned to grow and develop in the marketplace. Ultimately I would like to be an active participant in the organization’s positioning and would like to work in collaboration to create their strategy for success. Working with people that have strong values, innovative ideas, respect for each other and most importantly be committed to our mutual success is especially important to me.

Tags for this Online Resume: Medical Affairs, Scientific Strategy, KOL Management, Regulatory , Vendor Management, New Product Commercialization

Regulatory Affairs - 15 Years of Experience - Near 94565

Regulatory Affairs professional seeking to change industries for petrochemical regulatory matters to biotech and medical device industry. Proven aptitude to in dealing with regulatory authorites with special expertise in the Asia Pacific region.

Clinical Regulatory Affairs - 19 Years of Experience - Near 80004

Clinical Regulatory Affairs - 13 Years of Experience - Near 19711

My background includes six years experience as a Project Manager for Regulatory Global submissions, as well as Life Cycle Management of Regulatory documents. As a Project Manager within the Submission Management Group, I provided expertise on global submission compilation and published electronic submissions compiled in RSS Application (eCTD) in accordance with Health Authority guidelines and departmental standards.

Tags for this Online Resume: Newark, DE, eCTD, RSS Application, Regulatory Publisher, Regulatory Submissions, Document Management, Legal, Management, Project Management, Publishing, Quality Assurance, Test, eCTDXpress

Clinical Regulatory Affairs

Regulatory Affairs CMC - 8 Years of Experience - Near 62446, Cuernavaca, Mexico

Clinical Regulatory Affairs

Worldwide Director of Regulatory Affairs

Strategic Regulatory Affairs Professional with diverse and progressive experience leading growing or established companies in the pharmaceutical, biotech and medical device industry providing global strategic regulatory direction for both new and existing products, as a primary contact facilitating preparation of international regulatory documents. Advances the development of knowledge, products, people, collaboration, c...

Tags for this Online Resume: Product Registration, CMC, International Submissions, Global regulatory, BLA, INDs, Orphan Drugs, Project Management, Bilingual, International regulations

Clinical Regulatory Affairs

Clinical Regulatory Affairs - 20 Years of Experience - Near 21702