Clinical Data Management Jobs in Illinois
Job Title: Clinical Data Manager Position Description Working knowledge of Good Clinical Data Management Practices, Good Clinical Practices, Good Manufacturing Practices, Clinical research, Clinical trial process and related regulatory requirements and terminology. Working knowledge of Clinical database applications such as EDC preferably the InForm system. Solid understanding of the clinical tria...
Perform clinical care and compliance reviews utilizing published measures and criteria from the National Committee for Quality Assurance (NCQA), Medicare, accrediting bodies, and other organizations. Work with providers and nursing staff to implement actions to improve results. - RN or LPN with license in good standing in the State of Illinois. - Experience in medical record review and statistical...
Seeking experience with translational medicine, biomarker identification and companion diagnostics in the contect of Cancer therapeutics development to oversee operations and project management for globa pharmaceutical company. Shall manage lab and clinical operataions including following activities: * Participate in the identification, selection and development of biomarkers and diagnostics for t...
JOB DESCRIPTION CLINICAL COMPLIANCE ASSOCIATE CLINICAL SERVICES I. Responsibilities A. Analyze various funding, contract, compliance, outcome and quality measures to assure new and on-going clinical compliance with all requirements B. Develop training materials, guides, quick reference materials and presentations for clinical staff use in understanding various payer standards, service limits and r...
.to use your skills and experience. This is the time to let your talent come to life. To maximize your knowledge and use it for the greater good. To work with the best professionals using state-of-the-art technology, and improve lives with your innovative ideas and ambitious dreams. Find a better way: the Sysmex Way. .to improve the lives of others. Headquartered in Kobe, Japan, Sysmex is located...
Responsible for managing the organization and conduct of regulatory and non-regulatory clinical programs in compliance with Clinical Operations policies and procedures, Regulatory (Health) Authority requirements and guidelines, and International Conference on Harmonization (ICH) Guidelines in support of global business objectives. Reports directly to the Medical Products Associate Director of Glob...
We are currently looking to hire Permanent Senior Regional CRA's The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOP and regulations. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data col...
Find a Better Way. .to use your skills and experience. This is the time to let your talent come to life. To maximize your knowledge and use it for the greater good. To work with the best professionals using state-of-the-art technology, and improve lives with your innovative ideas and ambitious dreams. Find a better way: the Sysmex Way. .to improve the lives of others. Headquartered in Kobe, Japan,...
Judge Healthcare is actively seeking a CRA( Clinical Research Associate) for a leading Bio Pharma client in the Lake Forest, IL area. This is a project assignment slated to run from early January 2014 to early April 2014. PRIMARY FUNCTION: Supports and assists Clinical Project Managers (CPM) and the Clinical Operations team with execution of clinical research studies to develop safe and efficaciou...
Job Title: Clinical Affairs Coordinator Position Description Proven work history of being effective, accurate, time management and detail oriented. Strong communication skills and team player Computer literate and experience with data entry equipment and various word processing, spreadsheet and file maintenance programs Previous experience working in a medical environment and medical terminology,...
Description: The Director of Clinical Documentation Improvement is directly responsible for providing system level leadership for the clinical documentation improvement (CDI) program. The Director will work to leverage performance, providing feedback and influence to continually improve documentation results and impact key performance indicators. The Director drives continuous improvements in the...
Job Title: Sr. Clinical Research Associate Position Description Position is with the Women’s Health team supporting the conduct of a Phase 3 clinical study Position Responsibilities Key activities include review of clinical data, CRO and Vendor management, development and update of protocols/amendments, prepare study updates, assess compliance with the protocol, manage drug expiry, review vendor i...
Job Title: Clinical Project Manager Position Responsibilities Assist Sr. Project Manager (SPM) in planning and management of one or more clinical studies Assist SPM in the coordination of activities of cross-functional areas for the initiation, conduct and completion of one or more clinical studies on time and within budget Coordinate study activities such as study design, protocol preparation, in...
Job Title: Clinical Project Manager (Non-MD) B Position Overview Assist CRM for one or more clinical studies. Assist with management of CFO and vendors such as CROs, Central Lab and other suppliers. Matrix management of functional area leads to meet study deliverables. Is aware of both internal and external business environments and their impact on studies. Escalates performance issues to manageme...
Contract Position – H1’s/Subcontractors will NOT be considered: · Individual is expected to provide leadership within the Regulatory Affairs labeling group and will be responsible for actively contributing to the development and implementation of regulatory labeling strategy and documentation for marketed products and products in development. · Serve as the regulatory labeling representative on re...
Clinical Informatics Research Scientist (062971) – Chicago, IL Your challenge: To support our clinical research activities we are looking for a Clinical Informatics Research Scientist to bridge the gap between our clinical collaborators, encompassing medical staff and hospital IT personnel, and the back office in Philips Research North America. Your responsibilities: Build and expand an effective...
ICON Clinical Research Multiple
Home Based Clinical Research Associate Travel up to 80% ( Sites throughout the country) Phase I-IV experience desired Candidate can be based anywhere in the USA Perform assessment site visits to assure study implementation and monitoring activities are conducted according to expectations (as described in the monitoring plan ) The monitor adequately prepares for the Monitoring visit by reviewing si...
Xerox Corporation is a $22 billion leading global enterprise for business process and document management. Through its broad portfolio of technology and services, Xerox provides the essential back-office support that clears the way for clients to focus on what they do best: their real business. Headquartered in Norwalk, Conn., Xerox provides leading-edge document technology, services, software and...
Theradex® is an international contract reserach organization providing complete professional services for the clinical research and development of pharmaceutical compoounds, medical devices and diagnostic test in the areas of oncology and life-threatening diseases for over 30 years. Theradex® conducts studies which lead to marekting approval of significant advances; and has built a reputation on a...
Job Title: Site Manager Job Functions: • Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (or GCP compliance according to SOPs and/or client guidelines • Recruit investigators for participation in clinical trials • Negotiate study budgets with investigators • Obtain, review for appropriateness, and process regulatory and administrative documents from investigato...
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Clinical data Manager. Which is the best institute in USA?
I want to get certified as Clinical data Manager. Which is the best institute in USA for it? What are the prospects of getting a good job after the certification and in what range if anyone has any cl...
What the future of Clinical Data Management in Bangalore, India?
I'm a postgraduate in Biochemistry and I'm looking for a job in clinical research/data management, so pls guide me. Is clinical research job oriented or wet labs?
Should I go for a clinical data entry job?
I have done my MSc. Microbiology, would like to make a career in clinical data management field but right now I haven't done any clinical research course.In this case should I go for a clinical dat...
Healthcare Career Tools
Clinical Data Specialist
$31,200.00 - $92,597.00
Typical Salary for Clinical Data Specialist in Illinois
Source: Monster.com Careerbenchmarking Tool
Education / Training
Some College Coursework Completed
Source: Monster.com Careerbenchmarking Tool
Clinical Data Specialist
Maintains data and data quality by helping in the development and maintenance of protocol-specific clinical data management plans.
Rate of Growth
Size of Industry in 2006:
Source: Bureau of Labor Statistics, May 2006
Attention to Detail
Clinical Lab Testing
Processes clinical data including receipt, entry, verification, or filing of information.
Contributes to the compilation, organization, and production of protocols, clinical study reports, regulatory submissions, or other controlled documentation.
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