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Online Resumes with "Generate Protocols"
Manager preclinical studies, prepare clinical regulatory documents IRB/ICB submissions IND applications
My career objectives are to focus on clinical coordinator, study manager, quality assurance, and regulatory. For the last six years I have worked in preclinical testing drugs, getting them from pre-IND to IND submission and into the clinic. The next logical career move is to work in clinical.
Ideal Companies: All companies are ideal.
Tags for this Online Resume: Clinical Coordinator, Study Manager, Regulatory, Generate Protocols, Generate Case Report Forms, Preclinical study manager, Clinical, Stereotactic Neurosurgery, Tumor Models, Subcontracts, Office Manager
Summary of Qualifications Manufacturing engineering, experienced in both Research and Development (R&D) and operations. Generated Protocols and reports documenting validation of manufacturing equipment and processes to satisfy both FDA and CE requirements (e.g., IQ, OQ, PQ, ). Participated on a R&D team that brought new products to market from concept to finished goods. Conceptualized automation of a syringe manufacturing l...