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Database, Research, Cardiovascular, Clinical Research, Insulin, Query, Therapy, C-SECTION, Cesarean Section, Computer Aided Software Engineering
Over 15 years of Pharmaceutical and Medical Device Clinical Research Experience I will provide an employer with a highly qualified candidate to fill the role of Sr. CRA or Clinical Trial Lead.
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Protocol, Clinical Research, Data Reporting, Inventory, Medical, Medical Records, Research, Surgical, Documentation, Integrated Development Environments, oncology, clinical, phase, trial, gcp, protocol, pharmaceutical
Ideal Companies: Biomedical companies, pharmaceutical companies, hospitals in MA
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ELISA, Purify, Western blot, Cancer, Computer Aided Software Engineering, Printer Access Protocol, Billing, Call Center, Medical, Referrals
Ideal Companies: Clinical Research Organization, Biotech/Pharmaceutical Company
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Filing, Management, Compliance, Cancer, Quality, Quality Assurance, Quality Control, Test, Clinical Research, Research
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Clinical Research, Management, Protocol, Query, Research, Corrective Actions, Documentation, Monitoring, Project Leader, Project Management
3-years' experience coordinating and assisting in clinical trials monitoring activities * Sound knowledge of Good Clinical Practices (ICH-GCP) and FDA regulations * Vast experience in billing and coding, data management, data entry, conducting billing practices, and other administrative tasks * Familiar with various computerized coding programs and electronic health records. * Advanced medical/scientific knowledge and medi...
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Insurance, Audit, Compliance, Clinical Research, Data Management, Documentation, Filing, Management, Monitoring, Research
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Cancer, Data Queries, Monitoring, Query, Therapy, Antibiotic Therapy, Intensive Care, Clinical Research, ICH, Intensive Care Unit
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Monitoring, Protocol, Mining, Macromedia Flash, Management, Manufacturing, Documentation, Budgeting, C Programming Language, Cardiovascular
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. (...
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Research, Clinical Research, Management, Quality, Quality Assurance, Quality Control, Audit, Oracle, Filing, Good Clinical Practices
Ideal Companies: 1962, 1962, 1962
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Clinical Research, Data Queries, Documentation, Management, Research
Tags for this Online Resume:
Audit, Project Management, Project Manager, Training, Data Management, Financial, Financial Management, Management, Metrics, Procurement
