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Online Resumes with "TRIALs"
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
Vice President - 20 Years of Experience - Near 06484
ACCOMPLISHMENTS Instrumental in turnaround of Westchester Health Care Corporation. Workers' compensation reserves were $45M+ with loss potential of $258M. Created infrastructure for a dedicated Workers' Compensation unit. Developed best practices including a third party administrator and legal team overseeing medical component of claim management. Within 9 months reduced incurred costs by $3M and held stable over subsequent...
Tags for this Online Resume: leadership, change agent, CT, CA, NY,FL, workers'comp expert, HR VP, Risk Control, cost containment, Financial, Labor Relations, Compensation, management, Vice president
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)
Network Engineer
Profile Synopsis: I have been in the position of network engineer for almost 8 years in one of the esteemed financial Institution. I am an efficient and hardworking network engineer skilled on details and timely deliverables of the network requirements of the company's affiliated businesses. With sound knowledge of routing and switching, I have been working on B2B platform on multiple projects dealing with multiple third pa...
Tags for this Online Resume: Cisco, Connectivity, Extranet, Firewall, IPSec, Legacy, Networking, POD, Router, Routers
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
RESEARCH ADMINISTRATION PROFESSIONAL
Dedicated Clinical Research Professional with over 10 years' progressive experience managing multiple phases of clinical research projects. Possessing advanced education, leadership, management, diplomacy and organizational leadership skills and consistently demonstrating the highest level of personal and professional standards. Seeks a varied and challenging position that will enable me to consolidate my professional exper...
Tags for this Online Resume: Oncology, Clinical Research, Diversity, Research, Consulting, Immunology, Medication Adherence, Planning, Policy Development, Strategic Planning, clinical, research, clinical trials, cro, regulatory
