CV, Curriculum Vitae and Online Resumes Search

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Online Resumes with "Good Clinical practices"

Clinical Research - 6 Years of Experience - Near 37013

Accomplishments Significant flow cytometry assay development experience. Proficient in multicolor assay panel design. Comfortable with immunoassay concepts and data analysis. Successfully manage all reagent, biological specimen, and laboratory supply orders. Able to function harmoniously with a team and independently to complete tasks. Successfully initiated and completed training of two new hires and participate in various...

Tags for this Online Resume: Drafting, Quality, Quality Assurance, Quality Control, Troubleshooting, Cellular, Data Analysis, Good Clinical Practices, Good Laboratory Practices, Microsoft

General - 20 Years of Experience - Near 40100

• Qualified Protection & Control and Substation Automation Systems, high Voltage equipment with over 25 years at electrical substations up to 240 kV, Commissioning and testing of electrical equipment as motors, breakers, Transformer, Generators, PT’s, CT’s. • Great skills in installation, commissioning and maintenance with relay Digital Protection, control circuit, of Generator control panel (GCP), Automatic Voltage Regulat...

Tags for this Online Resume: Electrical Engineer, Protection , Automation, English Language, Gas Plants, High Voltage, Install, Power (Os Enhancemnt Tool, Power Systems, Electrical Engineer, Protection & Control and Automation Electrical Systems., Spanish Language native

Clinical Regional Monitoring - 3 Years of Experience - Near 0000

PROFESSIONAL SUMMARY Clinical Research Professional with various project experience from concept to development. Talents include in-depth knowledge of ICH guidelines SAE reporting and GCP auditing. Integral team-player with excellent communication skills CORE QUALIFICATIONS * Patient Recruitment & Screening * Detailed Documentation * Serious Adverse Event Reporting * Communicating with IRB for study proposal, approval and u...

Tags for this Online Resume: Clinical Research, Data Entry, Research, Audit, Communication Skills, Compliance, Documentation, Excellent Communication Skills, Good Clinical Practices, ICH

Clinical Research - 14 Years of Experience - Near 27523

Objective: Lead clinical/project teams, continuing to manage and mentor clinical research experts, using skills, experience, and wisdoms to increase operational effectiveness. • Experienced in mentoring junior CRAs and project team members, training large or small groups in various areas of the clinical trial process, creating executive and operational reports, managing project timelines, and monitoring clinical sites sho...

Tags for this Online Resume: Management, Project Management, Support, Training, Process Improvements, Customer Service, Clinical Research, Medical, Monitoring, Research, Analysis, Critical Thinking, clinical, trial, gcp, protocol, pharmaceutical, ich, phase, Mentor, Team Lead, phase iv, phase ii, phase i, research, phase iii, clinical trials, regulatory, cro

Clinical Research - 9 Years of Experience - Near 1

Liliana Andrea Sánchez Valencia is a Clinical Research Associate Sr. CRA at Inventiv Health Clinical Colombia S.A.S, based in Bogotá Colombia, where she completes project activities associated with monitoring functions of Phase I-IV clinical research studies while continuing to develop knowledge of the drug development process, Good Clinical Practices, and relevant regulations. Ms. Sánchez has therapeutic experience in the ...

Tags for this Online Resume: Clinical Research, Management, Research, Protocol, Query, Project Management, Project Manager, Documentation

Clinical Research - 7 Years of Experience - Near 37208

Summary of Qualifications Detail-oriented, enthusiastic, and highly motivated Research Professional with 19+ years of successful experience. Diverse background encompasses research, laboratory analysis, reporting, and project/study planning and execution experience. Skilled at ensuring compliance with Standard Operating Procedures (SOP), Good Clinical Practices (GCP), and applicable policies and regulations. In-depth knowle...

Tags for this Online Resume: Instrumentation, Research, Quality, Quality Assurance, Quality Control, ISO, Toxicology, Leadership, Automation, Chemistry

Correspondence Clerk - 16 Years of Experience - Near 60085

PROFILE: Motivated, results-oriented Professional with extensive clinical and regulatory knowledge (Good Clinical Practices, Food and Drug Administration, The International Conference on Harmonization and other regulatory requirements), has 16 years experience in clinical support activities with a broad array of clinical database software programs. Possesses exceptional interpersonal skills to develop and foster working rel...

Tags for this Online Resume: Documentation, Filing, Database, Documentum, Documentum (Wkflow Sw), Support, Clinical Management, Management, Quality, Audit, Clinical Documentation

Clinical Research - 9 Years of Experience - Near 45999

- 3 clinical research studies while developing an understanding of the drug development process Good Clinical Practices and relevant regulations. Perform management of study site activities to ensure the integrity of clinical data in adherence to all applicable regulatory guidelines and Standard Operating Procedures (SOPs). New experience oncology trials (lung cancer melanoma antigen-specific immune-therapeutics) RDE (elect...

Tags for this Online Resume: Clinical Research, Research, Oncology, Overdose, Cord Injury, SAP MM module, Application Support, Good Clinical Practices, Management, Support

Clinical Research - 12 Years of Experience - Near 32837

Profile: Clinical Research Professional with vast experience in Phases I- IV study trials in Oncology,

Tags for this Online Resume: Protocol, Good Clinical Practices, Quality Assurance, Test, Oncology, Management, Research, Clinical Research, Data Management, Phlebotomy, clinical, phase, trial, pharmaceutical, gcp, protocol, ich

Clinical Research

To apply my knowledge of FDA Good Clinical Practice guidelines/ICH guidelines, extensive site/field Clinical Director, Site Lead Study Management, in addition to my experience with various therapeutic areas of medicine, to a position as a Clinical Research Associate. Achievement: Co-Author on Two Research Article Publications

Tags for this Online Resume: Clinical Research, Documentation, Research, Management, Monitoring, Outsourcing, Policies and Procedures, Protocol, Training, Accounting

Clinical Regional Monitoring

Accomplishments: * Compliance- Maintained compliance with regulatory standards. Ensuring site staff was trained and followed all guidelines set forth by the FDA. * Implementation-Implemented a new tracking system that resulted in improved query resolution. * Documentation-Ensured study sites followed ALCOA to ensure accuracy of through precise documentation. * Patient Safety-Ensured quality control through following ICH/GCP...

Tags for this Online Resume: Audit, Compliance, Data Quality, Documentation, Forth Programing Language, Good Clinical Practices, ICH, Management, Monitoring, Protocol

Quality Assurance Manager / Vendor Manager - 20 Years of Experience - Near 60060

SUMMARY: Experienced, dedicated, Quality Assurance professional and trainer who provides the knowledge and skills to assist with and drive projects as part of a team or as an individual contributor. * 20+ years of experience in pharmaceutical research, 15+ in Quality Assurance * Experience with Good Clinical Practice (GCP) regulations, the International Conference on Harmonization (ICH), Good Laboratory Practice (GLP), Vend...

Tags for this Online Resume: Quality Assurance, Test, Clinical Research, Research, Audit, Management, Pharmaceutical Industry, Development Activities, Policies and Procedures, Vendor Management, Clinical, GCP, GLP, Training, Nonclinical research, Preclinical, Early phase clinical research