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Online Resumes with "Medidata "
Clinical Data Management - 7 Years of Experience
A Clinical Research Professional having around 7 plus years of experience in the industry. Have sound experience in Drug trials (pharmaceutical trails), phase I-IV studies with drug trials, Microbiology techniques, and Molecular diagnostics techniques. Having strong verbal and written communication skills, a great team player and fun to work with.
Tags for this Online Resume: Denver,, MEDIDATA RAVE, SPOTFIRE, EDC, Project management, risk based monitoring, centralised monitoring, QUERY MANAGEMENT, Research, Management, Medical, Database, Good Clinical Practices, ICH, Query, Support, Research, Management, Medical, Project Management, Query, Support, Test, User Acceptance Testing
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
Clinical Research - 4 Years of Experience - Near 60148
Tags for this Online Resume: Medidata RAVE, InForm, OC RDC, Serious adverse event (SAE) reconciliation, lab reconciliation, IVRS , , Microsoft Excel proficiency, Study lead, Client interaction
Clinical Data Management - 9 Years of Experience - Near 01821
SUMMARY * I am certified-RAVE Study Builder- Certification Sponsored by Cognizant & Medidata USA. I have 12 years of experience in Project Management, Clinical Data Management, Technical Support and Team Management,Overall 10 years of progressive experience in Clinical Data Management domain from study start up till DBL activities. I am experienced with all aspects of data management including project management, edit check...
Tags for this Online Resume: Management, Data Management, Pharmaceutical Industry, Quality, Quality Control, Team Lead, Document Management, Audit, Training, Quality Assurance
Developer - 7 Years of Experience
PROFESSIONAL SUMMARY * Over 9 years of Clinical SAS programming experience in a Pharmaceutical industry involving different Phases (I, II & III) of clinical trials. * Experienced in working closely with statisticians to provide SAS programming in analyzing clinical trials data and generating Statistical Analysis Files, Tables, Listings, Summaries and Graphs/Figures (TLFs) for the Integrated Summary of Safety (ISS) and Integ...
Tags for this Online Resume: Microsoft Windows, SAS, Structured Query Language, Unix, Microsoft Windows 7, Windows 7, PDF, Proc, Extensible Markup Language (XML), Microsoft Excel
Clinical Research - 15 Years of Experience - Near 92880
ACCOMPLISHMENTS * Worked with 50 different sponsor and CRO companies on various GI studies * Managed Bunion investigational study with 300 patients. * Three FDA audits without 483. * Met all recruitment targets within required study timeframe * Managed regulatory binder for studies, post start-up * In depth knowledge of Microsoft packages ( Word, Excel and power point) Experienced with Oracle, Inform, Medidata eDC programs ...
Tags for this Online Resume: Clinical Research, Oncology, Research, Computer Aided Software Engineering, Good Clinical Practices, Medical, Microsoft, Microsoft Excel, Microsoft PowerPoint, Microsoft Word
Clinical Research - 8 Years of Experience - Near 60169
Professional Summary A certified professional Clinical Research with 4 years of experience in Clinical Research coordination and a year experience as Clinical Study Associate. Expertise in QC of documents, remote Monitoring and supporting the management by handling the tasks of multiple clinical research studies managing eTMF's & designing Clinical Portfolio's from Sponsor end. Expert in liaising between different departmen...
Tags for this Online Resume: Document Management, Monitoring - Remote and onsite, Clinical Research coordinator, Device trials, clinical Research, Project Management, QC and QA, Pharmacovigilance, Ethics and compliance, regulatory, Clinical study Associate, Multiple therapeutic areas experience, Phase 1-4 trials, Audits and Inspection readiness, Multiple software and application experience - Veeva VAULT , Impact , Quest , Sentinel,Tesla, EDC experience- RAVE Medidata, IRT system experience Clinpace , Endpoint
Software Engineer - 14 Years of Experience - Near 27604
PROFESSIONAL SUMMARY I have over fourteen years of business industry experience as a software developer/engineer. Experience working with relational databases and software development methodologies including agile. I am proficient in a range of computer systems, languages, tools, development and testing methodologies. Summary: This project involved development and testing thoroughly the concepts of phase 1 of Clinical Acces...
Tags for this Online Resume: java, spring, hibernate, struts, Oracle, db2, xml, Documentation, ejb, xlt, adf, webcenter, javascript, ajax, html, jsp, jsf
Clinical Data Management - 14 Years of Experience - Near 28411
I am a Clinical Data Manager with 14 years experience in all aspects of clinical trial from early development to post approval. I am interested in using my extensive experience to join a Data Management group.
Tags for this Online Resume: Remote, Medidata Rave, Work from hom, Clinical Research, Early Development, Phase I-IV
Clinical Research - 12 Years of Experience - Near 78254
SUMMARY OF QUALIFICATIONS * Managed Phase I -IV and observational Clinical Research Trials for HIV/AIDS, HIV Vaccine trials, HIV and Hepatitis, Infectious Diseases, Hyperlipidemia, Diabetes, Renal CKD, Secondary Hyperparathyroidism, Vitamin D Deficiency, Diabetic Nephropathy, Allergies, Asthma, and Immunology, Hepatic therapeutical area, from HBV, HCV, Fatty Liver, Cirrhosis in the Liver, medical devices. * As an inhouse mo...
Tags for this Online Resume: PEDIATRIC, Pharmaceutical, Surgical, C Programming Language, Data Entry, Hepatitis, Hepatitis C, Research, Therapy, Cardiovascular
Senior Clinical Research Consultant/ Associate
I have 12 years of experience in the field of clinical research with more than 9 years of experience in the field of monitoring. I have worked as a sub-investigator and quality insurance manager as well. I earned my Doctorate of Medicine in Anesthesiology and Critical Care in India in one of the reputed institutes. I relocated to US in 2002 and started my career in clinical research since research was my passion during my u...
Manager, Clinical Data Manager - 12 Years of Experience
Tags for this Online Resume: OC , OCRDC, Rave , Inform, Data Management, Clinical , Medidata
