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Online Resumes with "Solid Tumor"
Clinical Research - 16 Years of Experience - Near 27616
PROFILE Senior Pharmacovigilance Officer with 10 years of experience in the Pharmacovigilance industry. Over the course of my career, I have been involved in Global/UK/European/US Phase I-IV studies covering a wide range of therapeutic areas to include infectious disease, oncology, neurology and cardiology. Specific areas of oncology include Non-Hodgkin's Lymphoma, cervical cancer, breast cancer, prostate cancer, hepatocell...
Tags for this Online Resume: Coding, Troubleshooting, Documentation, Oncology, Cancer, Cardiology, Critical Care - Neurology, Diagnostics, Hepatitis, Hepatitis B
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 - 15 Years of Experience
SUMMARY A highly experienced Clinical Research professional with considerable experience in all stages of clinical trial processes, gained within the Biotech, CRO and Pharmaceutical environments. Key experiences areas: CNS- Psychiatric/Migraine/Alzheimer/Seizure/Movement Disorders Epilepsy, Cardiovascular- Statins, Type 1 & 2 Diabetes, Infectious Disease- HIV, AIDS, Autoimmune (NMO), Medical Device-stents, valves, glucomete...
Tags for this Online Resume: Clinical Programs, Clinical Research, Research, Protocol, Cardiovascular, Management, COPD, Distribution, Oncology, Vendor Management
Clinical Research - 16 Years of Experience - Near 07052
SUMMARY: Clinical research professional with experience conducting and managing sponsor related clinical trials Phases I-IV following GCP and ICH requirements and guidelines. Clinical trial experience in various indications including Oncology (Solid Tumors, Prostate, Lymphoma and Renal Cell Carcinoma) and Cardiovascular (myocardial infarction, acute ischemic stroke, and Venous Thrombo-Embolism). Strong team player experienc...
Tags for this Online Resume: Management, Billing, Direct Patient Care, Integrate, Inventory, Inventory management, Medical, Medical Billing
Clinical Regional Monitoring - 20 Years of Experience - Near 18929
Seeking an opportunity with a Pharmaceutical, Biotechnology company or CRO as a Senior Lead Clinical Research Associate, Lead CRA, CRA Manager/Trainer (Mentor) and/or CRO Oversight Monitor to employ my 27 years of clinical research monitoring, management skills and CRA mentoring as well as19 years of Respiratory/Pulmonary and Cardiopulmonary critical care clinical medicine. Clinical Research Experience: Projects/Therapeutic...
Tags for this Online Resume: Pharmaceutical, Clinical Research, Research, Rheumatology, Biomedical Industry, Pharmaceutical Industry, Cardiology, Critical Care - Neurology, Critical Care - Respiratory, Neurology, oncology, clinical, phase, gcp, protocol, trial, ich
Clinical Research
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...
Tags for this Online Resume: Chemotherapy, Clinical Research, Collection, Gastrointestinal, Oncology, PEDIATRIC, Protocol, Support
Clinical Regional Monitoring
Summary of Qualifications: Over nine years as CRA and ten years as CCRC performing site management of phases I-IV clinical trials with large and mid-sized pharmaceutical sponsors and international CROs: INC Research/inVentiv Health Clinical, Pfizer, United Therapeutics Inc., Clinipace Worldwide (Formerly Paragon Biomedical), GeNO LLC, PAREXEL, Merck, Astra Zeneca/MedImmune, GlaxoSmithKline Actelion, Gilead Sciences, INO The...
Tags for this Online Resume: Management, Pulmonary, Clinical Research, Documentation, Research, Protocol, Allergy, Applications, Assessments, Biomedical Industry
Medical Sales Representative
Tags for this Online Resume: Key Accounts, Program in General Insurance, Training, Web, Web Portal, Web Technologies, Account Management, Active Server Pages, Cancer, Compliance
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
