Title: Clinical Data Coordinator II/III

Company: MedImmune, LLC

Location: Gaithersburg, MD

Salary: Unspecified

Job Description:

Participate in the data collection and management of moderately to highly complex clinical trials to ensure processing is completed with a defined timeframe.

Provide data management planning and coordination of CDM activities for multiple projects using knowledge of database management techniques to ensure the accuracy and integrity of clinical data.

Logically translate the data requirements from protocol to CRF to database structure utilizing understanding of database architecture and its impact on data management processes and eCRF/CRF design

Lead the design, development, testing and implementation of tools and activities that promote the timely completion of studies, e.g., database, eCRF/CRF, edit check programming, data listings;

Identify data trends and develop strategies for managing them as needed; Participate in User Acceptance Testing (UAT) for EDC studies

Participate in the development of data management strategies for multicenter/global studies of highest complexity; Act as a resource for CDCI and CDCII, providing technical expertise and training; Provide ongoing feedback regarding project issues to lead data manager or department management; BS/BA with a minimum of 3 years of experience; o HS diploma/some college with a minimum of 5 years of experience

3-6 years clinical data management experience (in a biotechnology or pharmaceutical company or at a Contract Research Organization); managing people/projects

Proficient in Microsoft Office, Oracle Clinical, Phase Forward InForm, medical coding dictionaries; Working knowledge of software utilized for external data review, i.e. I-Review, Cognos Reporting; knowledge of medical terminology

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To learn more about this position and apply online, visit www.medimmune.appone.com and search for Req 00244.

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To apply, visit medimmune.appone.com and search for REQ 00244