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Online Resumes with "phase ii"



Construction Project Manager - 30 Years of Experience-kUWAIT

Curriculum Vitae Khaled Mohamed Rabie Tel: 50510301/51504450 Khalidrabhie@yahoo.com Khalid.rabhie@falghanim.com Status: Married Nationality: Egyptian Education: Bachelor of Science in Civil Engineering, El Mansoura University, Egypt - May1985 Practical project management course, from IDC technologies. Certified by PMI – April 2009 Professional Experience: Current Position: Since October 2013till Date Company: Alghan...

Tags for this Online Resume: Structural Design, Bilingual, Computer Literate, Construct (App Dev Tool), Construction, Database, Fabrication, Infrastructure

Featured Profile

RN Medical Coder - 18 years experience

Remote Medical Coder experienced in with ICD-9CM, ICD-10, WHODrug, WHO-ART, COSTART and MedDRA coding practices. Knowledge of diseases, drugs, dictionaries, and coding conventions. Multiple compound ownership interfacing with Clinical, Clinical Data Management and Clinical Safety to ensure appropriate coding for report analysis. Responsibilities include the daily running of studies, documentation of all procedures, regular...

Medical or Health Services Manager - 10 Years of Experience

Career Summary Pharmacist by education, with 10 years of Industrial Experience in various domains of Preclinical and Clinical Research and Development as well as IMP Supply Chain Management. R&D Professional with 4 years of Clinical Research experience from within the CRO as well as Sponsor environment that includes PK/PD studies, Phase II, III and IV studies and more than 1 year of experience in Preclinical research labora...

Tags for this Online Resume: Clinical Research, Clinical Supply , Trial Management , Microsoft, Microsoft Excel, Microsoft Office, Microsoft Word, Microsoft Word, Clinical Research, Management, Research, Analytical Skills, Audit, Cardiovascular, Compliance, ENT

Regional Clinical Research Associate

Highly-motivated Senior Clinical Research Coordinator with over twenty years of experience coordinating Phase II-IV clinical trials. Proven ability to work independently and effectively with leading Investigator site and Sponsors to meet project goals. Seeking a Clinical Research Associate position with a dynamic and expanding organization.

Clinical Research

PROFESSIONAL SUMMARY Persistent, Organized and detailed oriented professional interested to pursue a position as a Clinical Research Associate (CRA) with a pharmaceutical / biotechnology firm where I can utilize my medical and clinical research knowledge along with my strong technical and procedural skills in clinical monitoring to meet the growing needs for clinical trials of new drugs in multiple therapeutic areas. CORE Q...

Tags for this Online Resume: Protocol, Clinical Research, Research, Complaints, Documentation, Interactive Voice Response, MDR, Voice

Featured Profile

Global Regulatory Affairs - 14 Years of Experience- New Delhi India 110021

Seeking assignments as a Global Regulatory Affairs Professional - NCEs, GENERICS- Pharma, Biotech products, Botanicals & Medical Devices in Global Regions and/or Quality & Compliance professional across the Pharma & Medical Devices Industry. Overall Profile * With overall 15+ years industrial experience, with 14+ years in the field of Global Regulatory Affairs, Compilation & Submissions of Technical Packages for IND/CTA, ND...

Ideal Companies: BBraun Medical Pvt Ltd, New Delhi, India, Glenmark Pharmaceuticals Ltd., Mumbai, India, Panacea Biotec Ltd., New Delhi, India

Tags for this Online Resume: Regulatory Affairs, Management, Medical Devices, Pharmaceutical Industry, IND/CTA, Formulations & APIs, Regulatory Audits & Compliances, NCEs/NMEs/Generics, CT, Regulatory Consultancy, Regulatory Due Diligence & Gap Assessment

Biochemist - 15 Years of Experience - Near 08854

• Senior Level Drug Metabolism Scientist recognized for managing and collaborating with cross-functional teams to produce consistently superior results in discovery and development within strict deadlines. • Extensive experience in the Pharmaceutical Industry includes preclinical discovery and development, enzymology, in vitro metabolism, phenotyping of Phase I and Phase II enzymes, enzyme kinetics, CYP inhibition/inductio...

Tags for this Online Resume: Drug Metabolism, In vitro, P450, Enzymology, Drug-drug interaction, Drug discovery, Drug development

Clinical Research - 20 Years of Experience - Near 07081

Vaud. L'Hôpital Cantonal de Fribourg Performed and led all start-up aspects for a Phase II multi-center study for Crohn's disease. Monitored 120 patients using a PAF antagonist for asthma, including pre-study visits, site initiations, monitoring, and close down. Wrote protocol and designed CRF for a methacholine challenge study. Monitored pharmacokinetic Phase I studies co-wrote final study report.

Tags for this Online Resume: Clinical Research, Research, C Programming Language, Consulting, Hepatitis, Hepatitis C, Pharmaceutical, Protocol, Filing, Health Insurance Portability And Accountability Act

Clinical Regulatory Affairs - 10 Years of Experience - Near 28201

SUMMARY OF EXPERIENCE: Experienced clinical research professional with more than 15 years in clinical and academic research that has acquired diverse experience in phase II and III clinical drug and device studies with knowledge spanning several therapeutic areas and indications.

Tags for this Online Resume: Protocol, Collection, Documentation, Costing, Consulting, Document Review, Management, Oncology

Biostatatician - 6 Years of Experience - Near 46802

Professional Summary: * SAS Certified Programmer with around 6 years of experience in clinical trials data analysis and reporting in Health care and Pharmaceutical fields. * Well-versed with clinical data analysis: analyzing clinical data, creating tables, listing and generating reports and graphs as per requirements, specifications and Statistical Analysis Plan (SAP). Experienced with SAS procedures such as Proc Format, Pr...

Tags for this Online Resume: Protocol, SAP, Clarify, Data Analysis, Documentation, ETL, Extensible Markup Language (XML), Extract Transform Load Tools

Clinical Research

SUMMARY OF EXPERIENCE Experienced in assisting Project Manager in Phase II/ III studies. Administrative, financial and technical support to the project manager and team members of assigned projects during any and all phases of the project (planning, initiation, monitoring, data management and reporting). Extensive knowledge of all tracking and reporting programs at PAREXEL. Training and set up of systems and policies. Assis...

Tags for this Online Resume: TMF Lead, Forecasting, Training, CMA, Accounting, Investigator Payments, Home Based, Financial, Management, Project Management, Project Specialist, Resource Analyst