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Online Resumes with "MEDIDATA RAVE"
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...
SUMMARY OF EXPERIENCE * Monitored Phases I, II, III, clinical trials in many therapeutic areas, including, but not limited to, Oncology, Cardiology, Dermatology, Infectious Diseases, Immunology, Women's Health, Gastrointestinal, Genitourinary, Neuroscience, in Adult and Pediatric (Otitis Media and Influenza) populations. * Managed multiple studies in various stages of conduct at as many as 15 study centers at any given time...
Experienced with data entry and management of various EDC's to include IMPACT, Medidata/RAVE and CTMS * Therapeutic experience includes: Infectious Disease, Oncology, CNS, General Medicine, Mens Health, Cardiology and Dermatology * Received IAoCR (International Accreditation of Clinical Research) accreditation in February 2017 * Taught Continuing Education courses in Computer Skills at Austin Community College in 2000 - 200...
Tags for this Online Resume: Attention to Detail, Cardiology, Clinical Research, Communication Skills, Data Entry, Dermatology, Management, Medical, Oncology, Problem Solving, clinical, phase iv, Clinical monitoring, Phase I-IV, CRO, phase i, phase ii, clinical trials, pharmaceutical, cro, phase iii
Pursuing a challenging career in an organization where I can apply my talents and education in a medical/scientific-related field. Qualification Highlights Proficient use of Databases: iMedidata RAVE, RTOG, GOG, Inform, Oncore, CTSU, SWOG, Clincapture. Oversee RNs are strictly following X-Chart requirements of study protocols. Reviews Expectancy Reports of all associates in our department to ensure data timelines are met. R...
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...
PROFESSIONAL SUMMARY: Experienced Clinical Research Professional seeking career advancement with a CRO where I can make a positive contribution by utilizing my clinical research expertise. In-depth knowledge of clinical trial policies and procedures, study protocols, GCP guidelines, ICH guidelines, regulatory clinical trial documentation requirements, IRB documents submittal, sponsor electronic data capture systems for data...