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Clinical Regulatory Affairs Online Resumes
Clinical Regulatory Affairs
Clinical Regulatory Affairs - 3 Years of Experience - Near 02115
Clinical Regulatory Affairs
Tags for this Online Resume: Richmond, VA, FDA, DEA, Regulatory Affairs, Arlington, VA
Clinical Regulatory Affairs
Clinical Regulatory Affairs
Clinical Regulatory Affairs
Clinical Regulatory Affairs - 20 Years of Experience - Near 52246
Research experience at Canadian and American universities. * Strong communication (both oral and written) and computer skills, and excellent organizational skills. * Highly motivated person, with strong analytical and problem solving skills, self-driven, but also achievement oriented team player. * Respectful of diversity KNOWLEDGE AND EXPERIENCE: Extensive research experience in Clinical trials research with adult human s...
Tags for this Online Resume: Data Management, Management, Research, Evaluate, Microsoft Office, Personal Computer, Research and Development, Allergy, Immunology, Pulmonary
Clinical Regulatory Affairs
Tags for this Online Resume: Research, Recruiting, Surgery, Services, Applications, Clinical Research, Connectivity, Distribution, Documentation, Imaging
Associate Director, Regulatory Affairs, Philadelphia/Princeton/Horsham 15 years experience
Associate Director, Regulatory Affairs, Labeling led multiple teams to support ANDA approval and continued compliance with regulatory guidelines. Extensive negotiation with FDA reviewers to bring products to successful approval. Developed and led numerous pharma training sessions both internally and externally. Conducted company and global partner GMP and Quality Assurance audits. Successfully managed all aspects of a globa...
Tags for this Online Resume: Regulatory Affairs, Regulations, SPL, PLR, Personnel Management, Project Managemetn, Labeling, FDA Negotiation, Training, Audits, Contract Development, Pharmacovigilance
Clinical Regulatory Affairs
Clinical Regulatory Affairs - 15 Years of Experience - Near 24534
Tags for this Online Resume: Query, Management, Project Management, Protocol, Ad Hoc Reports, Clinical Research, Data Quality, Good Clinical Practices, Query, Management, Project Management, Protocol, Ad Hoc Reports, Clinical Research, Data Quality, Good Clinical Practices
Global Regulatory and Scientific Documentations Intern
Highly motivated and committed individual looking for a career in Regulatory Affairs as well as Research and Development in the pharmaceutical industry. Currently I am working at Bristol-Myers Squibb in the Global Regulatory Department. Works well under pressure in a sustained energetic manner. Comfortable multi tasking in a rapidly changing environment. Given my science education as well as my previous work experience with...
Tags for this Online Resume: Lab Technician , Research , Regulatory , Clinical , Healthcare, Hospital , Pharmaceutical
