 Perform routine data entry including first and second pass validation as required Adhere to current data entry priorities using appropriate tools and resources Add and resolve QC notes to data fields Act as liaison for data management issues between SCHARP study teams and research sites Attend assigned SCHARP study team meetings and conference calls Assist in development of Case Report Forms for assigned studies Manage study data for assigned studies Assist in the maintenance of the study database including routine revisions or additions Monitor study data to insure the quality and completeness of the data submitted by implementing quality control procedures as appropriate per CDMS Generate QC reports for site review and correction as well as a variety of other reports as required Evaluate study data for protocol compliance Assist in production and review of Data Operations SOPs and WPGs Assist Data Operations staff in resolving non-routine data entry issues Perform additional tasks as appropriate and assigned 2+ years’ experience in the pharmaceutical/clinical research environment as Clinical Data Coordinator or equivalent role EDC experience required. Working knowledge of Medidata Rave highly desirable. Demonstrated expertise in relevant clinical data management activities Working knowledge of ICH/GCP guidelines and FDA regulations Familiarity with all phases of clinical trials and ability to adapt to study requirements Strong verbal and written communication skills. Ability to understand and follow instructions and guidelines; able to pick up new tasks quickly; willing to ask questions when a task is not fully clear Ability to exercise independent judgment within generally defined practices and policies. Shows good judgment in interpreting guidelines and in when to seek support Ability to work independently and to work efficiently under pressure A strong team player with optimistic attitude