CV, Curriculum Vitae and Online Resumes Search

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Online Resumes with "Clinical Trials"

Quality Coordinator

Professional Summary: * Certified clinical research professional with nearly 10 years of clinical research experience in the medical device industry. I have a wide range of knowledge with site and study management having worked as an In-house/Field CRA, Lead CRA and Clinical Trial Assistant. * Conducting: Qualification, Initiation and Close-Out monitoring visits for pre and post-market trials. * Start-up activities for both...

Tags for this Online Resume: Documentation, Management, Data Management, Budgeting, Clinical Operations, Clinical Research, Collection, Compliance, Contract Negotiations, Distribution

Financial Analyst

Professional Summary: * Manager for four years at Employer Insurance in SAS Reports, SAS Statistics and Modeling. * QA Supervisor, problem solver with the ability to encourage others in collaborative problem solving. Reviews of business requirements and functional specification of the software to the test specification of desire results. Programs went through cycles, using software development methodology such as Second Edi...

Ideal Companies: 1960

Tags for this Online Resume: Pc, Personal Computer, SAS, IBM DB2 Database, Cobol Programming Language, Enterprise Guide, Modeling Experience, Teradata, Teradata (NCR Data Warehouseing product), Insurance

Quality Coordinator - 20 Years of Experience - Near 06790

Profile ASCP certified Medical technologist with a MS in Management and Biomedical Technology with years of first hand experience in healthcare settings. 10 years of experience working in the areas of Quality, Regulatory, Drug Safety, Pharmacovigilance and Clinical Trial Management.

Tags for this Online Resume: Management, Clarify, Coding, Collection, Complaints, Data Entry, Documentation, Protocol, Triage, Quality Assurance

Clinical SAS Programming

Summary of Qualifications * Clinical and Statistical SAS Programmer: 15 years * SAS Certification: Base (2001, 2003) Advanced (2005, 2009) * PMP: Project Management Institute (2002, 2005, 2008) * Clinical Trials Design and Management Certificate: University of California San Diego, California (2003-2005)

Tags for this Online Resume: Macro (Predefined Code), Pc, Personal Computer, IBM, IBM DB2 Database, Oncology, Protocol, Ad Hoc Reports, Query, Unix

Clinical Research - 20 Years of Experience - Near 32828

My career objective is to become a part of your Organization and to apply my experience and knowledge during the conduct of clinical trials, with emphasis on safety, efficacy in accordance to ICH-GCP, FDA and study protocol guidelines. Further, I will always strive to accomplish efficiency and savings for clients, by developing effective monitoring tools

Tags for this Online Resume: Microsoft-Office, ICH-GCP, FDA-guidelines, CTMS, EDC, RAVE, Monitoring, Clinical trials, Cardiovascular, Management, Auditing

Clinical Research Pro

Highlights of Qualifications * Eleven years of public health, laboratory and clinical research experience * Skilled in database management for study design, data collection, verification and analysis. * Excellent verbal and written communication skills with proven effectiveness in organizing scientific content and making complex ideas and plans accessible to a wider audience * Thoughtful collaborator and independent thinker...

Tags for this Online Resume: clinical trials, research, cro, Regulatory Affairs, Cancer, Clinical Research, Database, Management, Project Coordinator, Public Health

Clinical SAS Programming

SUMMARY: Over Nine years of experience in SAS programming with good knowledge of advanced statistical methodologies applied in Pharmaceutical and Biotech industries. Expertise in analyzing and reporting various phases (Phase I-IV) Of Clinical Trials using tools like Base SAS, SAS/STAT, SAS/GRAPH, SAS/SQL, SAS/MACRO, SAS/ACCESS and SAS/ODSin UNIX and Windows environment. Developing Debugging and validating the project-specif...

Tags for this Online Resume: Programming, Support, Microsoft Windows, SAS, SAS/STAT, Data Management, Management, HyperText Markup Language, Oncology, Macro (Predefined Code)

Clinical Research - 1 Years of Experience - Near 10710

Areas of Expertise * Direct patient contact * SOPs Implementation * FDA regulatory knowledge * Clinical Trials * Managerial

Tags for this Online Resume: Psychiatry, Data Management, Management, Accounting, Audit, Clinical Research, Data Entry, Evaluate, Forecast, Hepatitis

Associate Director Regulatory Affairs

I am seeking an opportunity to continue working in Regulatory Operations focusing primarily on eCTD submissions and document management of Regulatory, Clinical, and Quality compliance documents.

Tags for this Online Resume: Regulatory Affairs, Regulatory Operations, eCTD Submissions, Clinical Trial Master Files, Quality Assurance, Document Management

Clinical Research Coordinator, San Francisco

Looking for opportunities in the clinical trial/drug safety area in the pharmaceutical industry.

Tags for this Online Resume: Clinical Research Coordinator, Drug Safety, Medical writer

Early/Mid Level Statistical Analyst, San Francisco

I have 6 years of experience in clinical trials and healthcare research with the past 4.5 of those in a program management position. I currently manage a bipolar and depression research program at the VA in Palo Alto and Stanford University Medical Center. Working in this program has been a valuable experience where I've had the opportunity to develop many new skills (grant writing, scientific writing in general, managemen...

Clinical trial manager

Clinical trial research, conduct oncology, cardiovascular, diabetes, and neuro-degeneration disease trials, multi-center clinical trials and global trials.

Tags for this Online Resume: Publications, Protocol, Research, Cancer, Cardiovascular, Clinical Research, Critical Care - Neurology, Management, Neurology, Oncology