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Online Resumes with "Clinical Trial Data Management"



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 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 ...

CRA - 20+ yrs. Healthe Care, 6+ yrs. Clinical Research

Tags for this Online Resume: Clinical Trial Associate, Clinical Research Associate, Document Specialist, Clinical Trial Data Management

Clinical Data Management - 8 Years of Experience - Near 07083

SUMMARY * Senior Clinical Trial Data Manager with extensive experience in domestic and global trial data management * Deep expertise leading Phase I-IV trials, across various therapeutic areas, including Oncology, Cardiology, and Diabetes. * Adept at serving as the liaison between Sponsor and CRO/BPO. * Deep familiarity with ICH / GCP guidelines. Experienced with Medidata RAVE, and Oracle platforms, and likewise, skilled in...

Tags for this Online Resume: Clinical Research, Protocol, Research, Oncology, Audit, Management, Project Management, Data Manager, Rheumatology, Trend Analysis

Clinical Research

PROFESSIONAL SUMMARY: Experienced Clinical Research Professional seeking career advancement with a CRO where I can make a positive contribution by utilizing my clinical research expertise. In-depth knowledge of clinical trial policies and procedures, study protocols, GCP guidelines, ICH guidelines, regulatory clinical trial documentation requirements, IRB documents submittal, sponsor electronic data capture systems for data...

Tags for this Online Resume: Chemotherapy, Clinical Research, Collection, Gastrointestinal, Oncology, PEDIATRIC, Protocol, Support

Clinical Trials Executive - 25 Years Experience - Cincinnati

SUMMARY OF QUALIFICATIONS CRO professional specializing in central laboratory operations and clinical trials data management. Resolves issues by building consensus. Strong customer relationship skills developed as a service provider to the biopharmaceutical development community. Experience directing international teams to develop business intelligence enabling integrated business/IT strategic planning.

Tags for this Online Resume: Protocol, Management, Project Management, Applications, Information Technology, Business Development, Electronic Data Interchange, Insurance, clinical trials, cro, Data Management, Informatics, Innovation, Vendor Management, Business Process Management