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Online Resumes with "IMVs"
Creative Everyman
Educated professional with experience in creative writing, copy writing, press releases, public relations, customer service, web design, graphic design, print design, e-mail marketing, blogging, podcasting, and social media consulting for small businesses.
Ideal Companies: n/a
Tags for this Online Resume: blog, podcast, web design, print design, graphic design, html, css, photoshop, dreamweaver, creative writing, copy writing, copy editing, e-mail marketing, social media, public relations
Administrative Office Professional
Over 20 years administrative and customer service experience. Two years Human Resource experience,and over three years accounting experience.
Ideal Companies: No Specific
Tags for this Online Resume: Administrative, Human Resource
Clinical Research - 2 Years of Experience
SUMMARY OF EXPERIENCE Over 3 years of experience of clinical research experience with a clinical research organization. Established a reliable consultants building relationships with a strong commitment to quality. Team oriented, strong organizational skills with attention to detail Phase I-IV Experience. Ability to perform SWAT, PSSVs, SIVs, IMVs, and COVs according to company timeline and deadline. THERAPEAUTIC AREA OF EX...
Tags for this Online Resume: Management, Protocol, Clinical Research, Documentation, Research, Cardiology, Corrective Actions, Data Analysis
Clinical Research - 2 Years of Experience - Near 77449
HIGHLIGHTS OF QUALIFICATIONS: * RN with close to 2-years experience in clinical trials monitoring * Knowledgeable of clinical trial procedures and approval processes. * In-depth knowledge of ICH GCP guidelines and FDA regulations * Conversant with Design and Review of case report forms (CRF) * Conversant with Site Monitoring visits (PSVs, SIVs, IMVs and COVs) to meet study expectations. * Clinical and post-marketing safety ...
Tags for this Online Resume: Direct Patient Care, DRESSING CHANGES, Medical, Patient Care, Suctioning, Surgical, Wound Care, Acquired Immune Deficiency Syndrome (AIDS), HIV, Monitoring
Clinical Research - 14 Years of Experience - Near 77407
I have 5+ years of clinical research experience and I have developed the skills and abilities needed to be a great asset to the clinical research industry. I am seeking for a clinical research monitoring position where I can utilize my site monitoring skills and management experience to positively impact the clinical development campaigns of the client. Ability to travel nationally 80% of the time. I have experience working...
Tags for this Online Resume: Clarify, Clinical Research, CVS, Documentation, Drug Protocol, Good Clinical Practices, ICH, Project Leader, Project Management, Protocol
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
Clinical Regional Monitoring
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
Tags for this Online Resume: Accounting, Policies and Procedures, Project Management, Project Manager, Protocol, Documentation, Cardiology, Clinical Research, Orthopedics, Research
Not Listed - 0 Years of Experience
3-years' experience coordinating and assisting in clinical trials monitoring activities * Sound knowledge of Good Clinical Practices (ICH-GCP) and FDA regulations * Vast experience in billing and coding, data management, data entry, conducting billing practices, and other administrative tasks * Familiar with various computerized coding programs and electronic health records. * Advanced medical/scientific knowledge and medi...
Tags for this Online Resume: Insurance, Audit, Compliance, Clinical Research, Data Management, Documentation, Filing, Management, Monitoring, Research
