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Online Resumes with " GCP"
Research Director- 18 yeras if experience managing sites
I have over 18 years of professional experience established in clinical research. As my resume indicates, I have experience in all aspects of clinical trials. I recently worked as the Director of Clinical Operations in a clinical site where I performed all aspects of clinical trials and the daily operation including problem solving. I have successfully managed the quality assurance department and acted as a trainer for t...
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...
Clinical Research Professional - Specializing in Study Start Up
I am ready to take my career to the next level. I am a Clinical Research professional specializing in Study Start Up with experoence in: ICFs, Site Regulatory Packages, ICH-GCP, Feasibility and Contract Negotiation.
Tags for this Online Resume: ICH-GCP, Study Start Up, Informed Consent, Contract Site Agreements, Feasibility , Regulatory Documents
