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Online Resumes with "Clinical Research Associate CRA "
Clinical Research
Experienced Clinical Research Associate seeking a challenging and rewarding Clinical Research Associate (CRA) position that will utilize my clinical site monitoring and general management skills and experience to coordinate, monitor and manage all aspects of clinical trials in accordance with the ICH-GCP guidelines, FDA regulations, standard operating procedures and study protocol.
Clinical Research - 20 Years of Experience - Near 43003
Summary of Qualifications and Skills Graduate prepared nurse with a Clinical Specialist in Oncology with a minor in HIV Disease. Broad pharmaceutical experience, starting as a Research Coordinator in academia, an in-house Clinical Research Associate (CRA) in Biotech, Associate Director in Global Operations in Clinical Pharmacology with Aventis Pharmaceuticals, and as a home-based CRA Responsibly managed multiple projects an...
Tags for this Online Resume: Clinical Research, Research, Pharmaceutical Industry, Process Improvement, Project Leader, Project Management, Research and Development, Oncology, Medical/Surgical, HIV Disease, Long-term Care, Community-Based Care, Clinical Nurse Specialist, Remote Data Entry, Delaware, OH, Columbus, OH, Portland, OR, San Francisco, CA
Clinical Research Associate- 3 years Experience
To obtain a position as Clinical Research Associate (CRA) with a pharmaceutical / biotechnology firm where my knowledge and experience along with my strong technical and procedural skills in clinical monitoring can be utilized and challenged to meet the growing needs for clinical trials of new drugs and medical devices in multiple therapeutic areas. Also, to contribute to reducing the time it takes for a new drug to progres...
Medical & Clinical Laboratory Technologist - 20 Years of Experience - Near 07076
An accomplished scientist with proven track record in successfully managing complex scientific projects. Ability to work independently as well as to collaborate across functional areas. A positive inspirational personality combined the ability to pay attention to details. A hard working ethic and consistent delivery under strict timeline. A key contributor to many priority projects and publications.
Tags for this Online Resume: Clinical Data Management, Medical Writer, Oncology, Clinical Research Associate (CRA), Regulatory, Pharmaceutical Research, Clinical Coordinator, CMC, New Jersey, Clinical Trial Management, Medical Affair, SAS and Oracle Clinic
Clinical Research - 20 Years of Experience - Near 30016
SUMMARY * 23 years as a Clinical Data Management working for the following companies: Novartis, PRA International, Abbott, Covidien, Ingenix (i3), Ortho Clinical Diagnostics, Octagon Research Solutions and Pharmanet i-3. * 20+ years' experience of team leadership working with: Data Manager, Clinical Data Coordinator (CDC), Data Entry Personnel, Biostatisticians, Programmers, Investigators and Clinical Research Associates (C...
Tags for this Online Resume: clinical , Data, Manage , Reasar, Data Manager, Query, Coding, Quality Assurance, Test, Medical, Audit, Clinical Research
Sr. Clinical Research Associate - 22 years Experience - remote - Austin, TX
A top-performing Senior Clinical Research Associate with extensive experience in clinical research, GCP, ICH, Regulatory, and clinical site management/monitoring. Solid background in critical care nursing for in-depth understanding of medical terminology for records review. Highly skilled in spearheading internal teams through clinical research and document management to ensure accuracy and adherence with study specific str...
Ideal Companies: Pharmaceutical, Biotech, Medical Device, CRO
Tags for this Online Resume: Clinical Research, Management, Protocol, Research, Documentation, Medical, Allergy, Monitoring, Reporting Tools, Cardiology, clinical, trial, gcp, protocol, pharmaceutical, regulatory, medical device, CNS, EDC, contract, remote, CRO
Not Listed - 0 Years of Experience
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...
Tags for this Online Resume: Insurance, Audit, Compliance, Clinical Research, Data Management, Documentation, Filing, Management, Monitoring, Research
