CV, Curriculum Vitae and Online Resumes Search

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Online Resumes with "Therapeutic area"

Programmer - 7 Years of Experience - Near 08807

Experienced with CDISC SDTM (IG 3.1.2 and 3.1.3) and ADaM (IG 1.0) standards. * Created safety, and efficacy SDTM and ADaM datasets, summary tables, listings and graphs (TLFs). * Proficient at using SAS data step and procedures. * Experienced in generating Integrated Summaries of Safety and Efficacy (ISS, ISE). * Validated Analysis datasets and TLFs using parallel programming and other validation techniques. * Created new m...

Tags for this Online Resume: Operating Systems, Pharmaceutical, Pharmaceutical Industry, Proc, Programming, Protocol, Quality, Quality Assurance, Relational Database, SAP, java, it jobs, javascript

Senior Medical Scientist

I am a Medical Scientist with extensive clinical development experience and a proven track record of successful contributions to the approval of multiple new drug applications (NDA/BLA). I have a strong foundation of global drug development and extensive experience conducting clinical trials in accordance with local, country-level and global standards. My experiences range evenly from early to late stage clinical developmen...

Tags for this Online Resume: Cancer, Statistical Analysis, Cardiovascular, Chemistry, Diagnostics, Filing, Immunology, Integrate, Management, oncology, trial, pharmaceutical, clinical

System Engineer

Experienced with CDISC SDTM (IG 3.1.2 and 3.1.3) and ADaM (IG 1.0) standards. * Created safety, and efficacy SDTM and ADaM datasets, summary tables, listings and graphs (TLFs). * Proficient at using SAS data step and procedures. * Experienced in generating Integrated Summaries of Safety and Efficacy (ISS, ISE). * Validated Analysis datasets and TLFs using parallel programming and other validation techniques. * Created new m...

Tags for this Online Resume: Active Directory Application Mode (ADAM), Base SAS, C Programming Language, C++ Programming Language, Catalogs, Communication Skills, Compliance, Data Analysis, Data Management, Database

Clinical Research

To apply my knowledge of FDA Good Clinical Practice guidelines/ICH guidelines, extensive site/field Clinical Director, Site Lead Study Management, in addition to my experience with various therapeutic areas of medicine, to a position as a Clinical Research Associate. Achievement: Co-Author on Two Research Article Publications

Tags for this Online Resume: Clinical Research, Documentation, Research, Management, Monitoring, Outsourcing, Policies and Procedures, Protocol, Training, Accounting

Clinical Research

PROFILE Decisive, action-oriented and results-focused professional offering more than 30 years of experience in the medical field with 23 years focused in clinical research. Thorough knowledge of Medicine. Ability to deal with the public in a professional, concerned manner and ability to convey a sense of confidence and trust to patients and work well with other health professionals. Knowledgeable of FDA, ICH and GCP guidel...

Tags for this Online Resume: ICH, EKG, Research, C Programming Language, Catalogs, Clinical Research, Hematology, Hepatitis, Hepatitis C, Scheduling

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 Data Management - 8 Years of Experience - Near 07083

SUMMARY * Senior Clinical Trial Data Manager with extensive experience in domestic and global trial data management * Deep expertise leading Phase I-IV trials, across various therapeutic areas, including Oncology, Cardiology, and Diabetes. * Adept at serving as the liaison between Sponsor and CRO/BPO. * Deep familiarity with ICH / GCP guidelines. Experienced with Medidata RAVE, and Oracle platforms, and likewise, skilled in...

Tags for this Online Resume: Clinical Research, Protocol, Research, Oncology, Audit, Management, Project Management, Data Manager, Rheumatology, Trend Analysis

In Between - 5 Years of Experience - Near 500081

Career Summary * SAS Certified Base for SAS9 with more than four years of experience. * Worked on different Phases of clinical trials and I have experience in programming, SDTM, ADAM and reporting in Clinical Research using SAS environments. As a Clinical SAS * Worked on Various Complicated SDTM domains like LB, MO & OE for ophthalmoscopy studies * Understanding of the study Documents and Data (e.g. Study design and objecti...

Tags for this Online Resume: A SERIES, Active Directory Application Mode (ADAM), Base SAS, Cardiology, Clinical Research, Data Management, Documentation, Generate Reports, HyperText Markup Language, Macro (Predefined Code)

Case Manager - 20 Years of Experience - Near 21224

SUMMARY: 30 years Clinical Research and home-based monitoring experience 12 years Oncology monitoring experience 12 years Pediatric Nurse experience Largest workload: 5 - 6 protocols with 10-15 sites in Oncology-Non-Small Cell Lung-Phase III, Neurology-Multiple Sclerosis-Phase III while at EMD Serono 10 years experience with Inform EDC and 6 months experience with IMedidata Located 20 minutes from Baltimore Washington Inter...

Tags for this Online Resume: PEDIATRIC, Clinical Research, Research, Management, Therapy, Oncology, Protocol, Audit, Monitoring, Critical Care - Neurology, registered nurse

Clinical SAS Programming

SUMMARY OF QUALIFICATIONS * Certified SAS/Statistical programmer with over 7 years of experience in data analysis and statistical programming in phases I-IV of clinical trials working for Pharmaceutical companies and CROs in various therapeutic areas with high proficiency and within given timeline * Expertise in analyzing and coordinating clinical trial data, generating reports, tables, listings and graphs using SAS in acco...

Tags for this Online Resume: SAS, Proc, Programming, Data Management, Extensible Markup Language (XML), Generate Reports, HyperText Markup Language, Management, PDF, Pharmaceutical

Clinical Regional Monitoring - 12 Years of Experience - Near 30339

Profile A conscientious Research Associate with 30 years of diverse experience in product development, quality assurance as well as technical service and clinical research. A persistent self-starter experienced in operating and training personnel in a variety of analytical instrumentation and procedures. Successful in finding innovative solutions to a wide range of problems in a team environment or alone. inVentive Health C...

Tags for this Online Resume: Clinical Research, Research, Training, Management, Support, Technical Support, FRACTURES, Instrumentation

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