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 Clinical Data Coordinator - Ellicott City, Maryland

Details
Country: USA
Location: ELLICOTT CITY MD
Total applied: 40
Location: US-MD-ELLICOTT CITY

Base Pay:N/A

Employee Type:Full-Time Employee

Industry:Other Great Industries

Manages Others:No

Job Type:Research

Req'd Education:4 Year Degree

Req'd Experience:At Least 1 Year

Req'd Travel:Not Specified

Relocation Covered:No


Contact:Not Available

Phone:Not Available

Email:Not Available

Fax:Not Available



Ref ID:758356CBP


Company Links:Company Website
Clinical Data Coordinator - Ellicott City, Maryland

TEAMWORK The Ultimate Symbiotic Relationship Focusing on a common goal. Performing your job accurately so that the next person can do theirs. That's how we work together at ICON Clinical Research. Because at ICON, your personal best is the valuable link in the teamwork we need to achieve quality results.Working with ICON, you'll share in a unique culture of a large company that emphasizes a warm, friendly environment. This is where career possibilities can become realities... where those who look for challenges, embrace the learning and growth opportunities we offer.ICON Clinical Research is dedicated to providing the pharmaceutical and biotechnology industries with exceptional clinical research and biometrics services, and we're the first international CRO awarded ISO 9001:2000 quality certification across all divisions and functions.
Clinical Data Coordinators
Ellicott City, MarylandThe selected candidates will review Case Report Form (CRF) data for completeness, accuracy and consistency; identify and resolve data discrepancies; as appropriate, apply level I corrections to CRFs; generate and resolve (as appropriate) data queries; update/correct/review data in the clinical databases based on resolved data queries; perform data listings review; update tracking systems as necessary; create and maintain study files and appropriate study documentation.In addition to the above responsibilities, the Clinical Data Coordinator II may also assist with database testing, SSP preparation & review and other data management activities e.g. medical dictionary coding, SAE reconciliation, external data reconciliation.The Clinical Data Coordinator III will be responsible for setting up dummy data for testing, generating status reports for management, assisting the DBA with database development, and function as a co-lead on a study when necessary.The qualified candidates should have a degree in the life sciences or equivalent clinical data work experience. Accuracy and attention to detail is essential. Previous data entry experience is be a plus. Knowledge of medical terminology is a plus. At least one year of relevant experience required for the CDC II position. At least two years of relevant experience is required for the CDC III position.
Job Requirements
Come to ICON and be an important part of a well respected and growing company that believes the details of your career are every bit as critical as the work you do. You'll enjoy highly competitive benefits in addition to flexible scheduling, relocation assistance, tuition reimbursement, credit union, health club privileges, and many other exceptional advantages.TO APPLY and for more information on our opportunities and locations, please visit us at

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