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Customer Service Manager

Elizabeth, NJ
... Served as member of Ethics Committee to safeguard the rights, safety and wellbeing of clinical trial subjects. Radiation Oncology Data Manager 09/1984-10/1993 Presented cases during Tumor Board Rounds. Member of Ethic Committee. Verified that data ... - Aug 27

Management Clinical Research

Columbia, MD
... I managed the clinical and research operations of five clinical studies on carotid stenosis and peripheral vascular/arterial occlusive disease, and CREST-2 (Carotid Revascularization and Medical Management for Asymptomatic Carotid Stenosis Trial) ... - Aug 26

Clinical Research Project Manager

Katy, TX
... Collective experience in clinical trial designs from Phases I to Phase IV. Great attention to detail while collecting, authenticating and managing clinical trial data at multiple clinical sites across the country. Strong commercial awareness and ... - Aug 26

Management Training

Carlsbad, CA
... Practicing attorney adept at mediation with over 14 years trial law experience Versatile, collaborative and proactive ... Results: $4M in savings.`+ Consulted with leading edge Healthcare Insurance/Clinical Delivery organization as Interim V.P. ... - Aug 25

Clinical Research Microsoft Office

Edison, NJ
... Computer Skills Microsoft office- Word, Excel and PowerPoint SQL server, Internet search engines SUMMARY OF PROFESSIONAL SKILLS Source data verification TMF Management and organization Clinical Trial start up, close out Highly detail oriented ... - Aug 25

Medical Management

Saudi Arabia, Al Khobar, Eastern Province
... 6.On site primary investigator, clinical trial, Gilenya long term side effects. CERTIFICATION: 1.Neurology Board certified. 2.Neurophysiology Board eligible. 3.Epilepsy Board eligible. 4.Pain Board eligible. PROFESSIONAL MEMBERSHIP: 1.American ... - Aug 25

Clinical Research Management

... with all aspects of clinical research process. Familiar with all mine principals of dental management and organization of treatment plans and follow up process. Knowledgeable, of all requirements for Clinical Trial documents design, review ... - Aug 24

Clinical Research Associate

Houston, TX
... monitor and manage all aspects of clinical trials in accordance with the ICH-GCP guidelines, FDA regulations, standard operating procedures and study protocol. SUMMARY OF SKILLS: Phase I-IV clinical trial monitoring experience Knowledge of ICH ... - Aug 24

Data Entry Manager

Elizabeth, NJ
... into SharePoint 2010 Reconciliation of documentation and ensured that documents were available for every trial Support system to Clinical Trial Teams in navigation through SharePoint Delegated access on different levels, roles, responsibilities ... - Aug 23

Clinical Research Microsoft Office

Canada, Toronto, Ontario
... EXPERIENCE Clinical Research Project Plan and Preparation Reviewed of assigned protocols and other protocol documentation (ICF, IB) for accuracy, feasibility, timing, and resources. Prepared and maintained the Trial Master File (TMF) for the study. ... - Aug 22
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