CV, Curriculum Vitae and Online Resumes Search

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Online Resumes with "GCP "

Clinical Regional Monitoring - 11 Years of Experience - Near 53224

Tags for this Online Resume: clinical, trial, gcp, protocol, pharmaceutical, ich, phase, oncology, monitoring, site management

Clinical Data Management - 17 Years of Experience - Near 80023

To manage clinical trials projects and a project management level by delivering clean and on-time and within budget. To collaborate with multiple internal / external parties to achieve excellent year-over-year results.

Tags for this Online Resume: Management, Data Management, Reviews, Process Improvement, Protocol, Quality, Documentation, Process Improvements, Query, Oncology, oncology, phase, clinical, trial, gcp, protocol, sas

Program Manager - 10 Years of Experience - Near 92064

SUMMARY Project Manager/Portfolio Project Manager with significant experience in the healthcare and medical device research environment. Proven abilities to analyze business processes and markets excellent leadership, project management, and team building skills. Strong understanding of both medical device and pharmaceutical product development processes (GCP), as well as CLIA.

Tags for this Online Resume: Management, Project Management, Project Manager, Budgeting, Clinical Research, Financial, Financial Management, Oncology, PEDIATRIC, Pharmaceutical, Medical Device, Genomic Testing, Clinical Trials

Biochemist - 1 Years of Experience

Summary of Qualifications * Master degree in Science with more than 15 years' experience in educational and research setting. * Good knowledge of Ontario health care system and OHIP rules. * Very good knowledge of GCP, TCPS and procedures required for REB documentation. * Good computer skills on Microsoft Office programs and e-CRFs * Very good knowledge of research procedures as obtaining informed consent, drug accountabili...

Tags for this Online Resume: Coding, Research, Training, Accounting, Administrative Assistant, Communication Skills, Documentation, Good Clinical Practices, Data Entry, Data Management

Clinical Regional Monitoring - 15 Years of Experience - Near 30067

SUMMARY OF EXPERIENCE Experience in clinical trial coordination, including initiating, administering and maintaining protocols with emphasis on FDA compliance. Therapeutic areas of experience include Cardiology (Hypertension), Infectious Disease (Prostatitis and UTI), Diabetes, Obesity, Respiratory, Nephritis, Irritable Bowel Syndrome, COPD, GERD and Pain Management (Osteo-Arthritis). Phases include II, III and IV.

Tags for this Online Resume: Clinical Research, Research, Documentation, Protocol, Billing, Chiropractic, Document Review, Filing, Health Insurance, Insurance, clinical, trial, protocol, pharmaceutical, phase, oncology, gcp

Pharmacokinetist

Tags for this Online Resume: Pediatrics, Research, Allergy, PEDIATRIC, Sar, High Performance Liquid Chromatography (HPLC), phase, trial, gcp, protocol, pharmaceutical, ich, DMPK, pharmacokinetics, ADME

Animal Scientist - 20 Years of Experience - Near 19129

with Animal Surgery Province, Southwestern Minority -Teaching and research focussed on Endocrinology using radio immunoassay.

Tags for this Online Resume: Electrophoresis, ELISA, Research, Mcp (Os -Lg Unisys Sys), Medical, Project Management, Project Manager, Surgery, oncology, clinical, phase, trial, gcp, protocol, sas, pharmaceutical, sap, ich, animal surgery, mice, rats, cell culture, iPS cell, myocyte, mouse models of heart attack, heart feilure model

Clinical Research - 16 Years of Experience - Near 94547

SUMMARY of QUALIFICATIONS 16 years of experience as a Clinical Research professional in Biotech and Pharmaceutical industries. Well-rounded skill, as a CRA in Clinical Operations processes, Clinical Development, Regulatory, TMF and Data Management. Skilled in data audit/review Study start up, Study conduct, Vendor management, and Site monitoring activities extensive knowledge of GCP-ICH, GLP, GMP guidelines familiar with Ex...

Tags for this Online Resume: Protocol, Assessments, Audit, Clinical Research, Documentation, Pediatrics, Research, Clinical Management, Distribution, oncology, phase, trial, clinical, protocol, pharmaceutical, gcp, ich

Clinical In-house Monitoring - 4 Years of Experience - Near 95131

Tags for this Online Resume: Documentation, Protocol, Audit, Good Clinical Practices, ICH, Management, Quality Assurance, Test, Quality, Quality Control, oncology, clinical, phase, trial, gcp, protocol, pharmaceutical, SOP, CAPA, Regulation, ich, Monitor, Clinical research, Clinical Trial

Clinical Research - 7 Years of Experience - Near 27560

Tags for this Online Resume: Clinical Research, Research, Medical, Medical Records, Protocol, Documentation, Monitoring, PEDIATRIC, Pediatric Patients, Pediatrics, oncology, protocol, phase, clinical, gcp, trial, pharmaceutical

Clinical Research - 3 Years of Experience - Near 02478

Summary: MS in Clinical Investigation with 3+ years of experience as Clinical research assistant cum coordinator seeking a preferably full time position in Clinical Research fields as Clinical Trial Associate / Project Management. Offering combination of strong background in biological sciences (specialization in Oncology, Molecular biology) as well as deep understanding and knowledge of ICH-GCP & FDA regulations. Demonstra...

Tags for this Online Resume: Clinical Research, Documentation, Research, Advertising, Audit, Budgetary, Data Entry, Data Management, Filing, Gastroenterology, Recruting, IRB admministration, regulatory, phase ii, clinical trials, ICH-E6 GCP and GLP, HIPAA compliance

Clinical Research - 20 Years of Experience - Near 07405

Tags for this Online Resume: Management, Project Management, Accounting, Business Development, Forecasting, Resource Allocations, Associate Customer Service, Chemistry, PMI, oncology, phase, clinical, trial, gcp, protocol, pharmaceutical, Real World Evidence, RWE, Late Phase, Interventional, Non-Interventional