Review study records in Client registry and perform relational QC as required between/amongst documents as needed.Provide reports to identify all required data points per study.Identify potentially incorrect and missing data points, and review total registry record with study team members.Instruct study team members on how and where to find required data point information, and collect information and location of applicable source documentation for data points from study team.Provide Data Entry Specialist with required information to make necessary entries/corrections to each study in the Client registry.Responsible for meeting client productivity metrics

Responsible for entering and correcting data for studies in the Protocol Registration System within The Clinical trials.gov database.

Assist study teams with both study management and data management activities Validate and monitor web-based data capture data flow, issue and resolve queries, track data review, report to team progress and trends Review validation work done by other team members to ensure all issues are resolved Establish and maintain key interactions with customers (internal/external) and interface with clinical departments to ensure quality of SD deliverables

Liaison between Contract Research organizations to ensure database setup and timely delivery of databases and other trial results Work closely with colleagues in order to relay clarifications to CROs Provide input in company development of processes and infrastructure concerning data management Assist with development and review of CRFs and associated documents, protocols and system setupReview and edit department SOPs Data Management Specialist 2005-2007; Assist with development and review of CRFs and associated documents, protocols and system setupLiaison between Contract Research organizations to ensure database setup and timely delivery of databases and other trial results Work closely with colleagues in order to relay clarifications to CROs Provide input in company development of processes and infrastructure concerning data management

Review Case report forms. Generate edit specifications and data review guidelines, edit query and resolve data issues Coordinate and interact with Clinical staff to resolve data issues.

Thoroughly review protocols and CRFs to assure functionality and compliance to standardsAssure system development tasks are accurately completed and perform final reviewFunction as a departmental technical resource and assist in development of new technical processes Represent Clinical Data Management in multidisciplinary settings and maintain communications between staff in European and US sitesEditing and resolution of inconsistencies and errors in data collected during investigational drug researchResponsible for assuring the quality completion of all work associated with assigned project and reporting project status routinely to appropriate personnel within Clinical Operations and CR&DGenerate and resolve Data Clarification Forms for assigned study sites through routine contactTracking data flow and monitoring of staff workloadTrain and mentor new employees in basic data management skillsLiaison between Wyeth project group and CRO Data Management Team Assist with migration of databases to Oracle Clinical

Function as a departmental technical resource and assist in development of new technical processes. Represent Clinical Data Management in multidisciplinary settings and maintain communications between staff in European and US sites.Liaison between Wyeth project group and CRO Data Management Team.

Perform all clinical data handling functions. Project Leader responsible for assuring the quality completion of all work associated with an assigned project.