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Online Resumes with "IRB"
MEDICAL ETHICS ADVISOR
I have had 20 years medical ethics training and advising. I specialize in end-of-life issues for hospitals and medical experimentation ethics. I serve on three Institutional Review Boards (IRB) and have passed the Certified IRB Professional exam.
Tags for this Online Resume: Sacramento, Part-time, 300/day, ethics trainer, medical/research, compliance, palliative care
Clinical Research - 3 Years of Experience
Basra studies: 1. Population-Based Study to Define the Clinical & Economic Burden of Pneumococcal Pneumonia in Hospitalized Adult Patients in Jefferson County, Kentucky (HAPPI). 2. PROTOCOL # B1851147 Streptococcus Pneumoniae Serotypes in Adults 18 Years and Older with Radiographically-confirmed Community-Acquired Pneumonia (CAP). * Screen different hospitals for eligible patients every day for many studies. * Approached an...
Tags for this Online Resume: Clinical Research, Infectious Diseases, Research, Audit, COLLECTED SPECIMENS, Data Entry, Distribution, Documentation
Professional Researcher - 10 Years Experience
PhD with documented success and experience in a diverse range of fields including academia, pharmaceuticals, and the medical device industry. Excellent writing, presentation and data analyses skills. Strong interpersonal skills with a remarkable ability to communicate scientific information to a diverse audience. Motivated by systems to improve human health and patient care.
Ideal Companies: Stryker, Johnson and Johnson, Glaxo Smith Kline
Tags for this Online Resume: Research, Infectious Diseases, Statistics, Medical Devices, Spine, Orthopedics, Sales, Pennsylvania, Clinical Research Manager, Biology, Immunological Assays, Client Relations, Social Media, Large-Scale Studies, Vaccines, Market Analysis, Event Planning, Sales Cycle Management, Data Analyses, qPCR, Genome Sequencing, Global Research, Journal Publications, Published Writer, Media Relations, Presenatations, Team Leadership
Lead Clinical Research Coordinator - 4+ Years of Experience - Near 48304
Tags for this Online Resume: SPSS, CCRP, IRB documents, Multicenter Clinical Trials, SAE reporting, Data management, internal monitoring, GCP and FDA regulations
Clinical Research - 20 Years of Experience - Near 60601
-Participate in development of new intramural clinical research studies, both for solid tumors and hematology/oncology, reviewed all new protocols, supervised designing case report forms for the new protocols for the solid tumors and hematology/oncology. -Work with the multiple investigators on developing and implementing new intramural oncology protocols and supervised accomplishments with all protocols' requirements. ...
Clinical Project Manager
Accomplished, dynamic professional experienced in synergizing communications between clinical research centers, contract research organizations (CROs), and major pharmaceutical corporations to amass clinical investigation objectives. Adept at executing, managing and monitoring IRB-approved, Phase I-III clinical studies and data management. Proven success in identifying opportunities to improve timely event reporting, increa...
Tags for this Online Resume: Clinical Project Manager, Clinical Team Lead, Clinical Research Manager, Clinical Research Associate
Clinical Research - 15 Years of Experience
Focused on obtaining a position as a Clinical Research Associate. Detail oriented with the ability to plan organize coordinate and manage projects according to priorities. Ongoing and consistent promotion of team work efforts. Excellent Communication and Interpersonal skills. Excellent oral and written communication skills with the ability to communicate effectively with medical personnel. Quick learner with the ability to ...
Tags for this Online Resume: Documentation, Management, Cardiovascular, Cardiology, Clinical Research, Distribution, Good Clinical Practices, Research
Administrative Assistant - 13 Years of Experience - Near 27713
SUMMARY Professional with extensive experience in various companies, including a leading IRB, a global 500 pharmaceutical company, and a national research university, with increasing responsibilities. Demonstrated abilities in customer service satisfaction, communications, project management, office administration, managing invoices, supervisory experience, and interpersonal dynamics.
Tags for this Online Resume: Data Entry, Distribution, Management, Policies and Procedures, Administrative Support, Email, Inventory, Inventory management, Quality, Quality Assurance
Clinical Regulatory Specialist
Looking for an opportunity that will allow me to share my skills and experience for the betterment of our global community. I have worked in this arena for quite some time and I know how to avoid the pitfalls surrounding clinical trials to ensure deliverables are met and compliance and efficacy is adhered to on every level of the study timeline.
Tags for this Online Resume: Clinical Trials , IRB Submisssion, Compliance specialist, Willing to Travel, Regulatory Document Reviewer, Essential Document reviewer, Informed Consent Reviewer, Management, Clinical Research, Ethics Committee Submission experience
Clinical Regulatory Affairs - Boston Area
Tags for this Online Resume: IRB, FDA, Clinical Research, Unix, Regulatory Affairs, NDA, GLP
Clinical Research Associate
SUMMARY: To apply my knowledge of FDA Good Clinical Practice guidelines/ICH guidelines, extensive site/field Clinical Director, Site Lead Study Management, in addition to my experience with various therapeutic areas of medicine, to a position as a Clinical Research Associate. AREAS OF EXPERTISE * Management * Interview candidates and either make a selection decision or recommend individuals for hire. * Able to manage multip...
Tags for this Online Resume: Clinical Research, Research, Accounting, Acquired Immune Deficiency Syndrome (AIDS), Advertising, Amazon Elastic MapReduce, Audit, Basic First Aid, BLS, Budgeting
Clinical Research
Summary of Qualifications Clinical Research Manager, Associate, Monitor, Coordinator, with over 25 years experience in the medical field and 21 years experience in clinical trials with extensive experience in the fields of Cardiology, Electrophysiology, Neurology, Urology, Autoimmune, Respiratory, Gastroenterology, Weight Loss, Diabetes, Women's Studies, Arthritis, COPD, Gynecology, Endocrinology, Rheumatology and Stem Cell...
Tags for this Online Resume: Monitoring, Protocol, Cardiovascular, Clinical Research, Management, Pharmaceutical, Research, Therapy, Audit, Data Management, Medical Device, CRA, CTM, Clinical Trials
