Clinical Data Coordinator-Data Management Project Leader, Ellicott City, MD

Success through teamwork

We work together to find a better way and break new ground to make progress possible. Focused on common goals, we raise the standard and make a difference. We strive for excellence in everything we do.

At ICON, career possibilities can become realities for those who look for challenges and embrace learning and growth opportunities.

ICON Clinical Research is dedicated to providing the pharmaceutical and biotechnology industries with exceptional clinical research and biometrics services.

To continue our legacy of excellence, ICON Development Solutions, a dynamic and innovative Product Development Organization committed to helping pharmaceutical and biotech companies bring products through development from early stage to regulatory approval, is now the Strategic Pharmaceutical Development Division of ICON.

Join us in one of our current openings and enjoy highly competitive benefits and exceptional advantages.

Clinical Data Coordinator - Data Management Project Leader
Ellicott City, MD
ICON Development Solutions

ICON Development Solutions is recruiting Clinical Data Coordinators and Data Management Project Leaders.
The Clinical Data Coordinator candidate will independently and accurately review Case Report Form data for completeness, accuracy, and consistency in accordance with all applicable procedures, will be responsible for performing Quality Reviews and identifying data discrepancies in the clinical data via computerized edits as well as manual checks/listings and appropriately address all issues. In this role you will independently and accurately generate data queries to resolve data discrepancies, prepare database test documentation and test data entry screens. You will also assist with the validation of edit check programs, represent Data Management at internal/external meetings as appropriate and effectively mentor less experienced staff and assume study lead role when applicable.

In addition, the Data Management Project Leader candidate will also be the primary contact with the sponsor and will be responsible for the management of project activities and resources, staff evaluations and training, and project documentation. In this role, you will write study specific procedures, alert sponsors of any issues, plan and allocate resources and ensure that the project is going as planned according to the timeline

Candidates should have a degree in the life sciences and/or relevant experience along with 2+ years of clinical data management experience in either a CRO or pharmaceutical company and experience using clinical data management software and/or medical terminology. The understanding of Protocol and CRF design and review, clinical database structure and annotated Case Report Forms, programming language skills, and knowledge of the Clinical Data Management process is required. Must be detail-oriented, able to multi-task, and possess excellent communication skills. The employee may occasionally lift and/or move up to 40 pounds. Occasional travel (less than 10%) may be required.

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 http://www.iconclinical.com/index.asp?getpage=true&sid=10&ssid=173 . Please apply to Req. #293459, #293460 or #293461. No agencies, please.

ICON. A Symbol of Excellence.

ICON Clinical Research is an Equal Opportunity Employer committed to strength in diversity.

www.iconclinical.com
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