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Online Resumes with "NDA"
Regulatory Affairs Associate
Fulltime opportunity in Regulatory Affairs Function
Tags for this Online Resume: Regulatory Submission, ECTD, PDF Editor, SPL, Regulatory Compliance, Regulatory Compliance/FDA/EMA (EU), Clinical Trials, NDA/ANDA/IND/CTA, Medical Devices
Director of Life Sciences Consulting
Lead a Life Sciences Practice and ultimately progress to the VP level.
Ideal Companies: Business and IT consulting firms in life sciences;professional services firms in life sciences.
Tags for this Online Resume: Program Director, Process Optimization, Systems Integration, Human Performance Optimization, Application Design & Development, Leadership, Research and Development, Clinical Research, Clinical Research and Development, Regulatory Affairs, Safety Surveillance, Marketing and Advertising, R and D
Clinical Regulatory Affairs
Tags for this Online Resume: regulatory affairs, quality assurance, clinical research associate, cGMP compliance, ISO 13485, NDA, IND, 510K, PMA, SOP, quality audit
Regulatory Affairs Associate, New Jersey
Regulatory Affairs professional with a strong regulatory and compliance foundation, well-versed in the laws, regulations and requirements of the FDA; over six years of experience as an International Coordinator for a pharmaceutical organization, currently completing a graduate degree in Regulatory Affairs in Drug Development, Biologics and Medical Devices, studying all facets of regulatory requirements including processes a...
Respiratory Therapist
TO BE ABLE TO LEARN AND DO BETTER ATMY PROFESSION.
In-vivo Pharmacologist
Extensive years of experience in the research, planning and implementation of in-vivo models in the Respiratory, Inflammatory and Oncology areas. Project management for various drug development models. Exceptional analytical and problem solving skills. Highly motivated, with the demonstrated ability to conduct independent research related to the successful development of pre-clinical and IND/NDA candidates.
Tags for this Online Resume: pharmacology, in-vivo, animal, dosing
Regulatory Affairs, Clinical Research, Quality Assurance
A degreed professional with over 4 years of experience in the pharmaceutical/Biotech industry with multi-functional Regulatory, Clinical and Quality background. Demonstrated ability to expand beyond the scope of assigned responsibilities to gain proficiency in new areas. Responsibilities have ranged from managing the preparation, submission of INDs, BLAs, ANDAs/NDA, to reviewing QMS, essential regulatory documents to ensure...
Tags for this Online Resume: Regulatory Affairs, Clinical Research, FDA, GCP, GCP, ICH, GLP, Pharmaceuticals, Quality Assurance
