Study Management Needed

SR. CRS (Phase I) OR (Phase II-III)

***20-30% Travel Required (Baltimore, DC area)

 

This Wilmington DE consulting position offers an opportunity to both study management and data management activities.  The ideal candidate will  monitor the web-based data capture data flow for assigned sites.  Job responsibilities will include data review, PELs and exception list reviews, issue and resolve queries, work with Regional CRAs to resolve data issues, track data review, report to team leader regarding progress and trends.  There will also be coordination operational aspects of study and participate in activities that ensure quality, consistency, and integration of study data and progress to time cost and quality from Study Delivery Concept through database lock and study close-out activities. The consultant will establish and maintain key interactions with customers and interface with clinical departments to ensure quality of  deliverables.  Along with Monitoring Study Conduct and progress, proactively identify and resolving  issues.  The consultant will lead in preparation and delivery of Study documents.  As well as ensure timely entry into communication tools.

 

Consultant must offer at least 2-5 years of Clinical Data Management experience.  Any clinical study monitoring experience is a big plus.  Outstanding communication and teamwork skills are required.

 

KEYWORDS:  Data Management, Clinical Research, Query, queries, validate, Validation, start up, lock, initiation, close-out, edit, edit-check, web-based capture system, edc, SAS, Oracle Clinical, ClinTrial, Rave, Medidata, data review, dmp, data management plan.

This opportunity offers a competitive market rate depending on experience!