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Online Resumes with "Therapeutic Experience"
Marketing & Mental Health Professional with extensive knowledge of communications combined with clinical therapeutic experience. Proven leadership, interpersonal, and organizational ability. Recognized for ability to work with very diverse clients and sta
I am a Senior Director in the pharmaceutical industry with experience in multiple therapeutic areas including specialty products. I have held leadership roles in Sales, Marketing, Managed Markets and Specialty Distribution. I have therapeutic experience in CV, Respiratory, Anti-Infectives, Anesthesia, Rheumatology, and GI. Most recently I have been involved in the launch of Renal/Dialysis and IBD with Specialty products.
PROFESSIONAL SUMMARY: A CRA with strong eye for detail and exceptional ability to interpret and follow instructions Possesses the ability to collect accurate data in line with client specifications excellent analytical and organizational skills knowledgeable in FDA regulations, GCP/ICH guidelines, seeking to join an organization that makes research subjects' safety its first priority. CORE QUALIFICATIONS: * Over 5 years exp...
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...
SUMMARY OF THERAPEUTIC EXPERIENCE Autoimmune Endocrine Neuroscience Oncology Ophthalmology Pediatric Studies Urology Women's Health SUMMARY OF PHASE EXPERIENCE Phase II Phase III Phase IV Device Studies SYSTEM EXPERIENCE: TransCelerate TrackWise OneNote Microsoft Lotus Notes
Therapeutic experience in IVD Oncology Hematology Orthopedics GI Cardiology Melanoma ENT Multiple Sclerosis and ADHD Extensive knowledge of FDA regulations ICH guidelines GLPs GCPs and SOPs * Monitoring experience of national and international sites for PSSVs SIVs IMVs and COVs * Ability to identify issues and resolve appropriately * Experience multiple EDC systems and platforms
SUMMARY OF CLINICAL EXPERIENCE Eleven years' experience as a CRA which includes 2 years as a Lead CRA in clinical trial monitoring, including study start up, study initiation through closeout, as well experience in International, and Domestic studies. Provide on-site clinical trial monitoring and full site management at investigational sites in the conduct of Phase II-IV clinical trials. Recruited and trained CRA (s), inves...
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
Profile: I have over 4 years' experience in the Clinical Research industry as a clinical research associate/ remote monitor and as a clinical research coordinator. My therapeutic strength is in Oncology (Solid), Infections and Infectious Diseases, Gastro- intestinal tract, pulmonology and with experiences on Phases I-III. THERAPEUTIC Experience: Oncology-Gastrointestinal (Carcinoid syndrome) Neuroendocrine tumors, Lymphoma ...
Liliana Andrea Sánchez Valencia is a Clinical Research Associate Sr. CRA at Inventiv Health Clinical Colombia S.A.S, based in Bogotá Colombia, where she completes project activities associated with monitoring functions of Phase I-IV clinical research studies while continuing to develop knowledge of the drug development process, Good Clinical Practices, and relevant regulations. Ms. Sánchez has therapeutic experience in the ...
- 3 clinical research studies while developing an understanding of the drug development process Good Clinical Practices and relevant regulations. Perform management of study site activities to ensure the integrity of clinical data in adherence to all applicable regulatory guidelines and Standard Operating Procedures (SOPs). New experience oncology trials (lung cancer melanoma antigen-specific immune-therapeutics) RDE (elect...