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Online Resumes with "clinical trial data"
Clinical Research Coordinator
Profile: Certified Clinical Research Associate professional with extensive recent focus in CVS research and clinical trials. Combine resourcefulness and problem solving skills with clinical knowledge to consistently deliver improved research and production results. Team player dedicated to quality, continuous improvement and bottom-line objectives. QUALIFICATION HIGHLIGHTS • Knowledgeable in all areas of research including...
Ideal Companies: quintiles, Pfizer, Novartis, Aerotek, Abbott, J&J, Merck
Tags for this Online Resume: CRA program, clinical research coordinator
Clinical Data Manager
Implemented knowledge of ICH GCP and CDISC Standards. Proven organizational skills with the ability to learn quickly; excellent time management, meet tight deadlines; manage multiple tasks and changing priorities while working in a high-pressured environment. Reputable for my attention to detail skills and strong ability to respond and solve problems in real time to fulfill customer expectations. Ability to work effectively...
Tags for this Online Resume: organized, data, bilingual, pharmaceutical, SQL Language, SAS, ClinTrial, ClinAccess, detail oriented
Clinical Trial, Data analysis, SAS Programmer
I am Biostatician with MS Degree and SAS Programming,looking any position inmy field or related.
Coordinator clinical trials, data manager, research, oncology
Data management positions, preferably home based, clinical trial coordination or specialist, full time with benefits and prospects for growth, continuing education
Tags for this Online Resume: research, data management, SAE reporting, oncology, neuroscience, liason, regulatory
Clinical Research Scientist, MD _Devices & Surgical Metods Development_4 years experience
Physician with clinical training in Internal Medicine and over nine years of clinical research experience in Medical Device and Cell Therapy industries would like to utilize medical, clinical and laboratory science knowledge toward the development of new medical products and procedures.
Tags for this Online Resume: clinical research, scientist, clinical trial data analysis, implant procedure development, investigators training, cell processing
Clinical Data Associate/Manager - six years plus experience
Established this firm to leverage extensive clinical data management experience in supporting clients’ clinical trial laboratories as well as clinical trial data of various therapeutic areas. Working remotely, manages a variety of activities including high-volume clinical double data entry reconciliation and data validation of Phase I, II, and III clinical trial studies. Enhances client value by performing double data entry...
Clinical Pharmacologist (PhD)
A Study Co-ordinator (PhD in Pharmacology) with more than 2.0 year of experience in the pharmaceutical industry. Demonstrated ability to attain and maintain a working knowledge of GCP, schedule Y (Indian CDSCO guidelines), Clinical Trial Document (CTD), and applicable SOPs. Expertise in BA/BE studies, managing clinical trials data, formulating source documents and data collection charts and severe adverse event reporting. C...
Tags for this Online Resume: Clinical Pharmacologist, ClinicalPhamacokinetics, Clinical PK-PD, BABE studies, Phase III studies
Senior Associate Research Operations - 6 years Industry experience
I am a Life science professional with over 6 years of experience with data mining, interpretation/ writing and document formatting to regulatory guidelines and showcased timely completion of projects with cross functional teams.
Tags for this Online Resume: San Francisco, Clinical trial data management, non-clinical data management, competitive intelligence, Documentation, medical writing
Clinical SAS Programming - 3 Years of Experience near 48310
•Clinical SAS Programmer with over 3 years of experience in designing, developing, testing & validating applications in pharmaceutical and clinical research •Expertise in analyzing and coordinating clinical trial data, generating tables and listings •Proficiency with Base SAS, SAS Macros, SAS/Access, SAS/SQL, SAS/STAT, SAS/Graph, SAS/ODS and SAS/Reports •Knowledge in understanding the PROTOCOLS, CDISC Process (SDTM and ADa...
Tags for this Online Resume: base SAS, Advance SAS, SAS-MACROS, SAS- ACCESS, PROC SQL, SAS- STATS, SAS- GRAPHS, PROC REPORT
Clinical SAS Programming - 5 Years of Experience - Near 08809
Dear Sir/Madam, Greetings. I am Krishna, Cheyula-Venkata and I am having 5 years of experience in SAS Programming in Clinical Trials. I am a SAS Certified Base and Clinical Trials programmer using SAS 9. I am a permanent resident here in USA and I can start the new contract in two weeks. I have good experience in clinical trial analysis activities for phase I, II in CVS and CNS therapeutic areas. Solid experience in compl...
Tags for this Online Resume: sas, macros, sdtm, adam, cdisc, TFL, validation
Clinical trials Assistant
I have a graduate degree in Health Care and currently pursuing Level 1 Certificate in CTRA at Durham Technical Community College. I have also completed the GCP training . Currently I am working part time for 6 to 8 hours per week as a translator in a company that conducts and monitors the cognitive testing for clinical trials. I am seeking an entry- level or an internship position, in the field of Clinical Trials and Data ...
Biostatatician - 6 Years of Experience - Near 46802
Professional Summary: * SAS Certified Programmer with around 6 years of experience in clinical trials data analysis and reporting in Health care and Pharmaceutical fields. * Well-versed with clinical data analysis: analyzing clinical data, creating tables, listing and generating reports and graphs as per requirements, specifications and Statistical Analysis Plan (SAP). Experienced with SAS procedures such as Proc Format, Pr...
Tags for this Online Resume: Protocol, SAP, Clarify, Data Analysis, Documentation, ETL, Extensible Markup Language (XML), Extract Transform Load Tools