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Online Resumes with "drug accountability"

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 Research - 10 Years of Experience - Near 08002

PROFESSIONAL SUMMARY * Research Nurse with over 10 years' experience * Therapeutic areas of experience include Cardiovascular, Oncology, Medical Device, Immunology, Pediatrics, Neurology, Rheumatology, Phases I-IV. * Skilled with sponsor and Investigator-initiated research projects * Multiple site management dealing with Europe, Asia, South America * Team Lead responsible for oversight of clinical research staff, time manag...

Tags for this Online Resume: Protocol, Research, Management, Documentation, Cardiology, Audit, Budgeting, Clinical Research, Critical Care - Neurology, Data Entry

Clinical Research

PROFESSIONAL SUMMARY: Experienced Clinical Research Professional seeking career advancement with a CRO where I can make a positive contribution by utilizing my clinical research expertise. In-depth knowledge of clinical trial policies and procedures, study protocols, GCP guidelines, ICH guidelines, regulatory clinical trial documentation requirements, IRB documents submittal, sponsor electronic data capture systems for data...

Tags for this Online Resume: Chemotherapy, Clinical Research, Collection, Gastrointestinal, Oncology, PEDIATRIC, Protocol, Support

Featured Profile

Clinical Regional Monitoring - 15 Years of Experience - Near 75219

Professional Summary Accomplished and energetic Senior Clinical Research Associate with a solid history of achievement in monitoring clinical trials. Motivated leader with strong organizational and prioritization abilities. Performed lead study duties to include trip report review and expense reporting. Mentored junior level CRAs and provided feedback and constructive critiques. Interested in senior positions as a research ...

Ideal Companies: Allergan, Bayer, CMED, Novartis, Pfizer, Paidion Research,

Tags for this Online Resume: Clinical Research, Research, Medical, Medical Records, Monitoring, Documentation, Protocol, Complaints, Nursing, Ophthalmology