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Online Resumes with "Clinical Studies"
Clinical Studies Manager - 7 Years of Experience - Near San Antonio, TX 78213
Clinical Administrative Assistant and Documentation Quality Assurance - 6 Years of Experience - Near 46038
To become a highly contributing member of a healthcare system or corporate setting where I can utilize, sharpen, and expand my professional experience, knowledge, and skills.
Tags for this Online Resume: Document Management, Good Clinical Practices, Proofreading, Research and Development, Protocol, Fishers, Indiana, Strong Organizational Skills, Keen Eye for Detail, Proficient in Word, Excel, and Outlook, Familiarity with Clinical Regulatory Documents, Screening and Recruitment, Investigator Notebook, Dedicated and focused
Clinical Research Specialist
To overlook and organize medical research activities and manage clinical trials in all areas of the medical field. To communicate and interact with different business entities that involve in the initiation and operation of clinical trials for the purpose of establishing a quality and integrated systems that will objectively and truly evaluate and assess new pharmaceutical products and devices. To deliver successfully the d...
Tags for this Online Resume: Clinical Research, Clinical Study Coordinator, Clinical Research Manager, Clinical Trial Coordinator, Clinical Research Associate, Clinical Research Monitor
Clinical Research - 20 Years of Experience - Near 07081
Vaud. L'Hôpital Cantonal de Fribourg Performed and led all start-up aspects for a Phase II multi-center study for Crohn's disease. Monitored 120 patients using a PAF antagonist for asthma, including pre-study visits, site initiations, monitoring, and close down. Wrote protocol and designed CRF for a methacholine challenge study. Monitored pharmacokinetic Phase I studies co-wrote final study report.
Tags for this Online Resume: Clinical Research, Research, C Programming Language, Consulting, Hepatitis, Hepatitis C, Pharmaceutical, Protocol, Filing, Health Insurance Portability And Accountability Act
Clinical Research - 6 Years of Experience - Near 10461
Accomplished Clinical Research Professional with over 6 years’ experience in Clinical Study Manage- ment and hands-on skills in all spheres of clinical study process including but not limited to site manage- ment, study monitoring, all types of site visits, study start up and close out as well as data management. I wish to work with a team that will enhance my clinical research knowledge and broaden my scope.It is fulfill...
Tags for this Online Resume: georgia, Oncology, respiratory, CNS, Texas, Cardiovascular, New york
Clinical Studies / SAS Programmer / Analyst
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
Administrative Project Management - 20+ years- Indianapolis
SUMMARY Business professional with a broad range of experience in administrative and managerial roles within various corporate, academic, and non-profit organizations. Strong organizational skills in the areas of project management, data management, bookkeeping, and payroll. Extensive experience in clinical study coordination, clinical marketing, and creative promotional media. Exceptional interpersonal and communication sk...
Tags for this Online Resume: Administrative Assistant, Management, Project Management, Payroll, Data Analysis, Data Entry, Data Manager, Data Reporting, Marketing Management, Patient Education, Bookkeeping, Clinical data, Health and Wellness
DMPK-Clinical Research - Near 95035
SUMMARY: A holder of a PhD in Pharmacy from University of Bath/ UK, whose thesis was focused on Biopharmacy/Pharmacokinetic. I have hands-on experience Pre-clinical / Clinical studies within PKPT group for developing and implementing the bio-distribution, and PKPD relationships of novel chemo-immune therapeutics. My experience covered clinical development and documentation experience Summary for qualifications
Tags for this Online Resume: Oncology, Cardiovascular, Clinical Research, Compliance, Distribution, Pharmaceutical, Pharmaceutical Research, Progress, Protocol, Research, DMPK, Statistical Analysis, WinoNonlin
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 - 10 Years of Experience - Near M1T3N
SUMMARY: * NIH trained Study/Site Coordinator with 10 years of experience in clinical research coordination and administration. * Demonstrated ability in coordinating & implementing Network / Pharmaceutical / Investigator-driven multisite Phase I - IV clinical studies. * Adept in liaising with internal and external stakeholders.
Tags for this Online Resume: Protocol, Clinical Research Associate, Infectious Diseases, ICHGCP, Logistics of study material, Monitoring, Data Entry, Team Lead, Essential Documentation, Informed Consent, SOPs, Coordinator, Regulatory, QA/QC, Source Docmentation, CRF's, TMF, EDC, Toronto, Contracts, SAE
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
