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Online Resumes with "Clinical Trial Master Files"
Clinical Reaseach Assistant II, Milpitas
Worked s a clinical research assistant for 5 years, creating clinical documents, preparing central files,edc data entry and verification, inventory management. Lab instruments calibration, operation and maintenance. 8 years of experience as a QA technician
Tags for this Online Resume: medical device, Diabetes, YSI Blood glucose analyzer, Medidata, inventory control, clinical trial master file
Clinical Research - 6 Years of Experience - Near 92649
Experienced Clinical Research Professional interested in positions within the pharmaceutical or medical device industry.
Ideal Companies: inventiv, johnson & johnson, covance, covidien, peregrine
Tags for this Online Resume: Irvine, CCRP, regulatory affairs, clinical project manager, EDC, budgets , timelines, contracts and budgets
Clinical Research - 20 Years of Experience - Near 12553
SUMMARY Self-motivated, dedicated and hardworking professional with greater than 30 years of experience in Clinical Operations (Clinical Associate, Trial Master File, Grants & Payments) and Clinical Development & Medical Affairs within the pharmaceutical industry. Major strengths include excellent communication and organizational skills. CORE STRENGTHS Knowledge in Clinical Trials and Drug Development for Clinical Developme...
Tags for this Online Resume: Clinical Trial Associate, Immunology, Clinical Operations, Medical, Medical Affairs, Oncology, C Programming Language, Cardiovascular, Database, Hepatitis, clinical, phase, oncology, trial, protocol, gcp, pharmaceutical, ich, TMF, Clinical Payments, sap
Associate Director Regulatory Affairs
I am seeking an opportunity to continue working in Regulatory Operations focusing primarily on eCTD submissions and document management of Regulatory, Clinical, and Quality compliance documents.
Tags for this Online Resume: Regulatory Affairs, Regulatory Operations, eCTD Submissions, Clinical Trial Master Files, Quality Assurance, Document Management
Clinical In-house Monitoring - 17 Years of Experience - Near 08844
10+ years of proficient experience into clinical research as a Clinical research associate in pharmaceutical industries and clinical research organizations. * In-house and regional monitoring experience in Phase I, II, & III. * Capable to work as both in-house CRA and as a Regional CRA with efficiency to monitor and manage any number of sites depending on Sponsor's SOP. * Good working knowledge of GCP and ICH guidelines. (...
Tags for this Online Resume: Research, Clinical Research, Management, Quality, Quality Assurance, Quality Control, Audit, Oracle, Filing, Good Clinical Practices
