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Online Resumes with "IRB "
Compensation or Benefits Specialist - 20 Years of Experience
Summary An accomplished Payroll/HR professional who has provided expertise for over 25 years. Recognized as a business partner who is results-oriented and accepts and meets new challenges through the use of problem solving, organizational and interpersonal skills. Works exceptionally well in a business environment where teamwork and accountability are valued. Well versed in all areas of Wage and Hour law and has a strong ba...
Tags for this Online Resume: Payroll, Audit, Bank Reconciliation, Kronos, Kronos (Labor Mgmt Sys), Management, Acquisitions, Journal Entries, Month-end Close, Pricing
Clinical Regional Monitoring - 18 Years of Experience - Near 08053
Tags for this Online Resume: Clinical Research, monitoring, Cancer, Prestudy, initiation and close out visits, Inflammatory Diseases, Cardiovascular, regulatory review, Good Clinical Practices, New Jersey, Phase I - III Clinical trials, EDC, drug accountability, infectious diseases, laboratory and study supply, IRB documentation
Application Support - 17 Years of Experience - Near 80205
SUMMARY Experienced Operations Systems Analyst with 20+ years in Information Technology, Operations, Billing, and Vendor management. BSS/OSS, ITIL (foundation), ITSM, Service Now, eTOM. Strengths include the proven ability to adapt to changes in the workplace, work well independently or as part of a team. Being detail oriented and producing quality work with consistent results. Technical Proficiencies Billing: Martin, CBP, ...
Tags for this Online Resume: Billing, Voice, Management, Ds3, Install, Order Entry, Customer Accounts, Troubleshooting, User Datagram Protocol, Vendor Management
Clinical Research - 7 Years of Experience - Near 77449
Experienced professional seeking to fill a challenging career with a company willing to utilize my clinical, medical, and management skills.
Tags for this Online Resume: Research Manager, Good Clinical Practice GCP, Clinical Research Coordinator, IRB, Clinical Trials, FDA Regulations, Patient Care, Protocol, Assessments, Clinical Research
Clinical Research - 10 Years of Experience - Near 20895
SUMMARY: International work experience in Pharmacovigilance, Clinical Trials, Pharmaceutical Sales and Regulatory Affairs encompassing Phase I experimental trials through post marketing safety reporting for the National Institutes of Health and for major pharmaceutical companies. Accomplishments include: Work Instruction Manual on Data Reconciliation for Astrazeneca. Led a team of six in writing the Work Instruction Manual ...
Tags for this Online Resume: Team Lead, MedDRA, RN, Acquired Immune Deficiency Syndrome (AIDS), oncology, Drug Safety Monitoring, Quality Assurance, Quality Control, Clinical Research Support, Data Management, Pharmacovigilance, FDA Reporting, IRB, International experience, Product Launch
Clinical Research
Areas Of Expertise * Good Clinical Practices * QC/QA Audits * IRB Submission/Standards In-House Monitoring * TMF Subject Matter Expert * eTMF System Validation Research Site Management * Cross-Functional Collaboration * Clinical Operations
Tags for this Online Resume: TMF, eTMF, CCRP, Site Management, Informed Consent, GCP, Document Management, IRB, Clinical Operations, Regulatory, Contracts, Budget
Clinical Research - 3 Years of Experience
Summary * Highly qualified clinical research professional with over 17 years' experience, including Phase I-IV domestic and international studies (including EU, Eastern EU, South America, Asia, and Canada) in a wide range of therapeutic areas. * Experienced in all stages of study development from start up to close out with ability to view study progress by each data point or from a more global prospective. * Skilled at effe...
Tags for this Online Resume: Clinical Research, Oncology, PEDIATRIC
Scientist
SKILLS SUMMARY * Authored technical reports, research manuscripts, SOPs, IACUC and IRB review of protocols. * Knowledge of GLP, ICH, FDA and NIH regulations, CITI training. * Reviewing, Editing, QC, and Finalization of documents and research grants. * Extensive knowledge of MS-Word, Excel, PowerPoint and Microsoft Access. * Proficiency in GraphPad Prism, FlowJo, Sequencher and Geneious. * In-depth scientific knowledge of Im...
Tags for this Online Resume: immunology, virology, clinical research, regulatory
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
Electromechanical Equipment Assembler - 13 Years of Experience - Near L6Z 1
MECHANICAL TECHNICIAN professional Profile 10 + years' experience manufacturing, installing and repairing machinery * Strong ability to troubleshoot hydraulic and pneumatic machines * Highly skilled in conventional machines which include lathe, drill, grinders and sharpeners * Experienced in installation, wiring set-up of PLCs, and industrial communication systems. * Highly developed ability to analyze, troubleshoot, mainta...
Tags for this Online Resume: Blue Prints, Blueprints, Injection Molding, Switches, Welding, Email, Reliability, Schematics, Automation, Install, Builder Machine & Maintenance Mechanic
Clinical Research - 12 Years of Experience - Near 15135
Profile: Medical background with extensive research, quality improvement, regulatory, consent writing, creation of protocol-specific tools for physicians and coordinators, local IRB and external/commercial IRB, Institutional Review Board Staff, institutional liaison with all external IRBs, HTML coding of all active AHN studies for our AHN.org research site Qualifications of outside researchers * Institutional boilerplate la...
Tags for this Online Resume: Pharmaceutical, Documentation, Research, Audit, Cancer, Centrifuge, Clinical Research, Coding, Compliance, Data Analysis, clinical, phase iv, phase iii, clinical trials, regulatory, cro, phase i, phase ii, pharmaceutical, research
Clinical Research - 3 Years of Experience - Near 02478
Summary: MS in Clinical Investigation with 3+ years of experience as Clinical research assistant cum coordinator seeking a preferably full time position in Clinical Research fields as Clinical Trial Associate / Project Management. Offering combination of strong background in biological sciences (specialization in Oncology, Molecular biology) as well as deep understanding and knowledge of ICH-GCP & FDA regulations. Demonstra...
Tags for this Online Resume: Clinical Research, Documentation, Research, Advertising, Audit, Budgetary, Data Entry, Data Management, Filing, Gastroenterology, Recruting, IRB admministration, regulatory, phase ii, clinical trials, ICH-E6 GCP and GLP, HIPAA compliance
