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Online Resumes with "Consent"
Medical Scientist - 14 Years of Experience
Profile: Professional in Clinical Research with Extensive Medical Knowledge and Academic Research Experience Summary of Qualifications Clinical Research Skills * Graduated with Master Degree in Clinical Investigation Sciences, with knowledge and experience in clinical research, clinical trials design, IRB application, informed consent writing, protocol design, and data analysis. As well as knowledge in epidemiology and publ...
Tags for this Online Resume: Cardiology, Progress, Research, Cardiovascular, Medical, Consulting, Data Analysis, Pediatrics, Training, Attention to Detail
Clinical Pharmacovigilance/Drug Safety - 10 Years of Experience - Near 19440
Summary Clinical Scientist/Clinical Data Analyst/Clinical Data Management/Project Coordinator/GLP auditor/Research Biologist with over 15 years experience in the pharmaceutical industry. Authored/QC review of protocols, protocol amendments, protocol clarification letters, informed consent forms, risk language, periodic safety reports (PSUR, DSUR, QSR), investigator brochures, medical monitoring plans, clinical SAE narrative...
Tags for this Online Resume: Protocol, Oncology, Audit, Monitoring, Critical Care - Neurology, ICH, Neurology, Quality Assurance, Test, Data Quality
Construction Trade Worker Manager - 20 Years of Experience - Near 113
EXPERIENCE SUMMARY___________________________ * MEP and utility service project Design, Project Management, Estimation, Tendering, Material Approval, Procurement, Business Development initiations of Infrastructural, Residential, Industrial, Defense, Power, Hospital, Commercial, Multistoried & tower buildings. * MEP Design & Shop Drawings preparation, review & approval, the design of services and utility referring to the top...
Tags for this Online Resume: Business Development, Business Development Manager, Services, Substations, Water Supply, HVAC, Project Management, Project Manager, Billing, Progress, fire alarm, MEP Manager,, construction supervision Electrical, Mechanical & Plumbing services, shop drawing reviews, material procurement, value engineering
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
Medical Office Manager - 5 Years of Experience - Near 27502
QUALIFICATIONS: * Promoted to the Senior CRC position as the youngest individual within the organization due to ambition, diligence, a strong team player with the ability to look at the big picture and plan accordingly. * Developed strong CRO/sponsor/vendor relationships, ensuring continuity and open communications through all phases of the trials. * Continuously reached study goals by collaboration with a diverse populatio...
Tags for this Online Resume: Cardiology, Clinical Research, CMA, Communications, Management, Medical, Project Management, Research, Triage, Research Protocols, IRB, Informed Consent, Mentoring
Director or better
Stable company willing to invest in people Need to be in the Phila, central and southern New Jersey areas
Tags for this Online Resume: Management, Project Management, Documentation, Business Management, Forecasting, Pharmaceutical, Audit, Compliance, Quality, Quality Assurance, Validation, Regulatory Affairs, CQV, Consent Decree Remediation, Compliance Remediation
Psychology - 17 Years of Experience - Near 92057
Clinical Assisted Director of Operations in the daily operation of all trials at the Site. Responsible for staffing and training study personnel and planning study start-up activities. Responsible for team performance and annual goal reviews. Responsible for client relationships through obtaining feedback from trial monitors and sponsors. Trials was an outpatient Phase 2-4 clinical research facility with a 4-bed sleep labor...
Tags for this Online Resume: Management, Process Improvements, Risk Management, Clinical Operations, Clinical Research, Research, Pharmaceutical, clinical, phase iv, phase iii, pharmaceutical, quality, clinical QA, GCP, document control, clinical trials, IRB, consent document, essential documents, nonessential documents, SOPs, Work Instructions
Tax Manager - 10 Years of Experience - Near Portland, OR
Prepare Morrow is the largest tower crane and hoist rental provider in North America with a global network of full-service facilities with 27 locations in 6 countries. Primary Responsibilities: * Assist tax manager with all aspects of income tax filings for US/Canada federal, state, and local income tax returns for US parent and international subsidiaries * Review/prepare state and local/municipal sales and use tax and prop...
Tags for this Online Resume: Audit, Property Tax, Software, Filing, Real Estate, State Tax, Accounting, EMC, Management, SAN (Storage Area Network), accounting, tax, manufacturing, gaap, excel, accountant
Postsecondary Teacher - 11 Years of Experience - Near 29376
CURRICULUM VITAE: Sharon Woodruff Team excellence instructor, facilitator, and trainer. Proven managerial, interpersonal, and training skills. Work History Title: Senior Clinical Research Associate Company/Location United BioSource Corporation Kansas City, MO/Regional United States Dates July 2014 - January 2015 Accountabilities Implement and monitor clinical trials for medications and devices to ensure sponsor and invest...
Tags for this Online Resume: South Carolina, Training, New Hire , Business, Education, Postsecondary, Excellence
Human Resources Manager - 15 Years of Experience - Near 92122
I am a Human Resources professional with at least 15 to 20 years of experience in this field. I have at least 10 years employed as a manager responsible for managing Human Resources functions, supervising HR staff, and serving as a consultant to executives, managers, supervisors and lead workers. I have worked in environments in which the rank & file staff were in unions with collective bargaining agreements, and I have h...
Tags for this Online Resume: employee relations, human resources
Director of Nurses/Nurse Consultant 20 yrs. experience
Perform client/site visits as needed to provide education and training, general support, consultation, oversight and perform formal quality and performance evaluations/dashboards (open & closed chart internal audits). Areas of focus: Policy and practices, Staff education & development, Risk Management Indicators (Infection Control, Staffing, Medication Reconciliation & Tracers/ADR, Consents, Admit/Discharge, Treatment Pl...
Regional Home-Based CRA
Tags for this Online Resume: oncology, phase, clinical, trial, gcp, protocol, pharmaceutical, Cardiovascular, CRO, Neurology, Bone, immunotherapy, monitoring, Initiation, close-out, Remote, query, onsite, SOP, ICH, GCP, investigator, IRB, sponsor, CTMS, CNS, Endocrinology, Haematology, ICF, Informed Consent, EDC, SDV, InFORM, MediData Rave, eTrial, eDiary, MedWatch, Adverse Event AE, SAE, 1572 Statement of Investigator, IB, Trip Report
